BTE Technologies WER-1 MCU Wireless User Manual 40040005 rev 000

BTE Technologies, Inc. MCU Wireless 40040005 rev 000

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Users Manual Part I

40040005 rev. 000

USER MANUAL

40040005 rev. 000

BTE Technologies

Information in this document is subject to change

without notice. Companies, names and data used in

examples are fictitious unless otherwise noted. No

part of this manual may be reproduced or transmitted

in any form or by any means electronic, mechanical, or

otherwise, including photocopying and recording or in

connection with any information storage and retrieval

system, without prior permission from BTE Technologies.

BTE Technologies, Inc.™ may have patents or pending

patent applications, trademarks copyrights or other

intellectual property rights covering subject matter in this

document. The furnishing of this document does not give

you license to these patents, trademarks, copyrights, or

other intellectual property except as expressly provided in

any written license agreement from BTE Technologies, Inc.™

Printed in the U.S.A.

This manual supports the BTE Multi-Cervical™ Unit

Rev. 000

BTE Technologies

7455-L New Ridge Road

Hanover, MD 21076

Phone: 410.850.0333

Toll Free: 800.331.8845

Fax: 410.850.5244

service@btetech.com

www.BTEtech.com

40040005 rev. 000

Warranty

We guarantee that the BTE Technologies, Inc. rehabilitation products

are free of manufacturer defects in both workmanship and material.

We will replace or repair defective parts or equipment for a period

of time and in accordance with the conditions set forth below:

This warranty covers the structure and framework for 1 year of normal

institutional use. All mechanical components including bearings,

bushings, pulleys and glides are warranted from manufacturer

defects in both workmanship and material for a one-year period.

Cords and padding are covered for a 1-year period under normal use.

This limited warranty is in lieu of all warranties, expressed or implied

and all other obligations or liabilities on the part of BTE Technologies

Inc. We neither assume nor authorize any person to assume any other

obligation or liability in connection with the sale of this product.

Under no circumstances shall BTE Technologies, Inc. be liable by virtue

of this warranty or otherwise, for damage to any person or property what

so ever for any special, indirect, secondary or consequential damage of

any nature however arising out of the use or inability to use this product.

This limited warranty applies only while the BTE Technologies, Inc. product

remains in the possession of the original purchaser and has not been

subject to accident, misuse, abuse, unauthorized modification, failure

to follow instructional use, failure to do proper maintenance, incorrect

adjustments or failure due to cause beyond the manufacture’s control.

Disclaimer

The information presented in this manual is given in good faith and is

to the best of our knowledge accurate. However, anyone who uses this

information in any way does so entirely at his or her own risk. Neither BTE

Technologies, Inc., its officers nor their representatives can accept any

responsibility for any damage or injury incurred as a result of information

presented here except under the terms of the product warranty.

Class A Digital Device

This equipment has been tested and found to comply with the limits

for a Class A digital device, pursuant to part 15 of the FCC Rules.

These limits are designed to provide reasonable protection against

harmful interference when the equipment is operated in a commercial

environment. This equipment generates, uses, and can radiate

radio frequency energy and, if not installed and used in accordance

with the instruction manual, may cause harmful interference to

radio communications. Operation of this equipment in a residential

area is likely to cause harmful interference in which case the user

will be required to correct the interference at his own expense.

40040005 rev. 000

01 - Installation and Setup

02 - General Operation

03 - Client Information

04 - Templates

05 - Calibration

06 - Protocols

07 - Reports

08 - Cervical Conditioning

09 - Maintenance

10 - The Melbourne Protocol

USER

MANUAL

section 01

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40040005 rev. 000

01 - INSTALLATION & SETUP

Introduction 3

MCU™ Components 3

Multi-Cervical™ Station 3

Calibration Tools 4

Computer Equipment and Cart 4

Assembly Instructions 4

Setting up the MCU™ Station 4

Setting up the Computer Equipment and Cart 6

Strongly Recommended Additional Purchases 7

Computer Care 7

Check Computer Cables 7

Environment Requirements 7

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section 01

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40040005 rev. 000

INSTALLATION AND SETUP

I. INTRODUCTION

When you first look at the MCU™, it may be difficult to imagine that a cervical assessment can

be so simple. However, once you familiarize yourself with the basic components of the unit and

practice its operation following appropriate training, you will wonder how you ever did assess-

ments without it.

This MCU™ Operator’s Manual will review the basic components of the Multi Cervical™ Unit.

Once you are familiar with the components, you can explore the techniques and protocols for

performing a cervical assessment, including range of motion and isometric strength testing.

This Manual will also review the different types of reports that are automatically generated

using the information acquired throughout the assessment, as well as the clinical documenta-

tion you provide the Objective Documentation Evaluation System (ODES™) computer diagnostic

system component.

BTE Technologies recommends that the Multi-Cervical™ Unit be used in conjunction with a cer-

tified training program on The Melbourne Protocol. Two-day comprehensive training programs

are tailored to suit the specific needs of your facility. Refer to Section 10 for more information.

II. MCU™ COMPONENTS

A. MULTI CERVICAL™ STATION

The Multi Cervical™ Station consists of the base, column with weight stack, seat, halo,

weight stack pins, ROM stop, (2) head braces, (3) Velcro straps, and (4) RJ45 cables - 2

short and 2 long (Figure 1-1).

Figure 1-1. Multi-CervicalTM Station

Head Braces

Velcro Straps

RJ45 Cables

Base

Seat

Column

Halo

Weight Stack Pins

& ROM Stop

DO NOT CHANGE OR MODIFY ANY COMPONENTS

Any changes or modifications, especially to the wireless components, not expressly approved

by BTE Technologies, Inc. could void the user’s authority to operate the equipment.

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40040005 rev. 000

B. CALIBRATION TOOLS

The MCU™ calibration kit consists of (1) calibration block, (1) 10 lb.

weight, and (1) 15 lb. weight (Figure 1-2).

C. COMPUTER EQUIPMENT AND CART

The computer equipment consists of a computer cart, LCD monitor, CPU, printer, speakers,

isolation transformer, and a wireless hub (Figure 1-3).

III. ASSEMBLY INSTRUCTIONS

Once the MCU™ Station and computer cart have been unpacked, you are ready to start assem-

bling the unit.

A. SETTING UP THE MCU™ STATION

The MCU™ is shipped on casters to provide maximum protection in transit and ease of

installation. The caster assemblies provide adjustable ground clearance. The system is

shipped in the highest position to clear ramps, curbs, and thresholds, but it can also be

lowered to pass under low doorways.

Step 1. Move the MCU™ to the location you wish it to be used. Using a 3/4” wrench, lower

each caster a small amount until the MCU™ base is resting on the ground. Once the base

is on the ground, remove the casters (Figure 1-4).

Figure 1-2.

Calibration Tools

LCD Monitor

Computer Cart

Printer

CPU

Speakers

Wireless Hub

Isolation

Transformer

Figure 1-3. Computer Equipment and Cart

Lower the Casters Remove the Casters

Figure 1-4. Lowering and Removing the Casters

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40040005 rev. 000

Step 2. Locate the weight stack pins and ROM stop pin and place them in the correspond-

ing holes on the calibration plate (Figure 1-5).

Step 3. Locate the head braces and secure them to the calibra-

tion plate (Figure 1-6).

Step 4. Locate the Velcro straps and RJ45 cables. These may be placed on the computer

cart.

Step 5. Locate the calibration weights and calibration block and

place them in the triangular bracket on the base (Figure 1-7).

Step 6. Locate the 2 antennas and then locate the far-

right hole on the top back of the MCU™ station. Insert

one of the antennas through this hole and secure it to the

PCB (Figure 1-8).

Figure 1-5. Location of Weight Stack Pins & ROM STop Pin

Figure 1-6. Head Braces

Secured to Column

Figure 1-7. Location

of Calibration Tools

Figure 1-8. Attaching the

Antenna

ACCEPTABLE ANTENNA(S)

This device has been designed to operate with the antenna(s) listed below and having

a maximum gain of 2.7 dBi. Antennas not included in this list or having a gain greater

than 2.7 dBi are strictly prohibited for use with this device. The required antenna im-

pedance is 50 ohms.

Acceptable antenna(s) include:

1. Linx Technologies 916MHz 1/4 Wave Whip Antenna (ANT-916-CW-QW)

To reduce potential radio interference to other users, the antenna type and its gain

should be so chosen that the equivalent isotropically radiated power (e.i.r.p.) is not

more than that permitted for successful communication.

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40040005 rev. 000

Step 7. Locate the arm rests, note which is labeled left and which is right, and attach

them to the seat on the appropriate sides (Figure 1-9). Note that the armrest is inserted

below the plastic piece that is within the bracket.

Step 8. Plug the power cord, which is located at the bottom back of the MCU™, into the

designated wall outlet. Hold your hand above the back of the MCU™, next to the antenna,

and verify a red light shines on your hand; this confirms the PCB is receiving power (Figure

1-10).

B. SETTING UP THE COMPUTER EQUIPMENT AND CART

1. LCD MONITOR

If you haven’t done so, remove the small bag from the top shelf of the computer cart

and mount the LCD monitor to the cart (Figure 1-11). Plug the power cord and serial

cable into the back of the LCD monitor.

Threaded hole

on arm rest

Arm Rest Bracket

under Seat Insert Arm Rest

into Bracket

Arm Rest Knob

Thread Knob into

Threaded Hole Final Result

Figure 1-9. Attaching the Arm Rests

Figure 1-10. Plugging in the MCU

Figure 1-11. Securing LCD Monitor

Slide monitor

through brackets

Secure monitor

with set screw

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40040005 rev. 000

2. PRINTER

Remove the printer from its box and place it on the 2nd shelf of the computer cart. Fol-

lowing the instructions from the printer box, insert the ink cartridges and plug in the

power cord and USB cable. Once the computer is running and the printer is turned on,

print a test page.

3. CPU

Remove the CPU (computer tower) from its box and place it on the 3rd shelf of the com-

puter cart. Plug in the power cord, monitor serial cable, and printer USB cable.

4. SPEAKERS

Remove the speakers from their box and place them on the 3rd shelf of the computer

cart. Plug the cable from the left speaker into the designated jack on the right speaker.

Next, plug the power cord into the designated jack on the right speaker. Finally, plug the

speaker cable, which is attached to the right speaker into the CPU.

5. KEYBOARD & MOUSE

Remove the keyboard and mouse from their box. Place the keyboard on the auxiliary

shelf of the computer cart and plug the cord into the CPU. Place the mouse on the top

shelf of the computer cart and plug the cord into the CPU.

6. WIRELESS HUB

Locate the wireless Hub and place it on the 2nd shelf of the

computer cart. Note that inside of the Hub are magnets, which

are intended to keep the Hub stable on the shelf. Secure the 2nd

antenna (from Step 6 of ‘Setting up the MCU Station’) to the Hub

(Figure 1-12). Plug the USB cable into the CPU.

Note that is important to store the Hub in a location such that its

antenna is at least 3 feet from the antenna at the top of the MCU.

7. ISOLATION TRANSFORMER

Locate the isolation transformer and its power cord and place

it next to the designated wall outlet. Attach the computer cart

cable, which is located at the bottom back of the cart, to the

isolation transformer. Plug one end of the isolation transformer

power cord into the isolation transformer and the other end into

the designated wall outlet. Turn on the isolation transformer via

the green switch (Figure 1-13).

Figure 1-12. Place-

ment of Hub

Figure 1-13. Place-

ment of Transformer

The use of extension cords is not recommended. If an extension cord cannot be avoid-

ed, use no less than 14 gauge wire. Keep the cord as short as possible, and use only

hospital approved plugs. The extension cord MUST complete the ground from the ER

power supply cord to the wall outlet.

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40040005 rev. 000

IV. STRONGLY RECOMMENDED ADDITIONAL PURCHASES

In addition to the equipment shipped to you from BTE Technologies, the purchase of the fol-

lowing items from a local supplier is strongly recommended for adequate protection of your

patient data:

• Several “CD-RW” re-writable compact discs for backing up and archiving copies of patient

data

• An Uninterruptible Power Supply (UPS) unit providing at least 14 amps as a safeguard

against the permanent loss of patient information due to power surge or electrical power

failure.

• Disinfectant wipes to clean the commonly used surfaces on the machine and components.

VI. COMPUTER CARE

A computer’s hard disk is vulnerable to loss of data and “corruption” of data (may not function

correctly when you attempt to retrieve patient information) from a sudden change in the level

of electrical power. In the event of a power failure, the UPS battery will generate electricity

long enough to allow you to shut down the system without damage to your patient data.

Since computers are sensitive to extremes of temperature, do not place equipment close to a

direct source of heat or cold (for example, in direct sunlight, next to a radiator or an air condi-

tioner).

Do not install any additional software onto the controlling computer. The BTE Technologies

MCU™ system is in constant communication with the computer, so a “clean”, dedicated com-

puter system is crucial to the integrity of this communication system. Lastly, your computer will

not be covered under the warranty if any unapproved software has been installed.

A. CHECK COMPUTER CABLES

Check that all cables are securely connected to the computer. Just about every cable

connector is made in such a way that it will only attach in its appropriate location. If the

cables are not secured properly, there may be an interruption of the data transmission,

resulting in error messages.

B. ENVIRONMENT REQUIREMENTS

The MCU™ is designed to operate within the following environmental conditions:

Ambient Temperature: 50oF to 100oF (10oC to 40oC)

Relative Humidity: 30% to 75%

Atmospheric Pressure: 700hPa to 1060 hPa

Voltage Supply: 110-120 VAC (International Voltages differ)

IMPORTANT

In case of a malfunction, your computer can be repaired or replaced, but your valuable patient

data can only be restored from copies kept on “back-up” CDs (See Section 2 - General Informa-

tion).

IMPORTANT

Handle your computer with extreme care. A drop or a bump, even from a height of 3-4 inches,

may cause serious damage, which is not covered by the warranty.

section 02

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40040005 rev. 000

02 - GENERAL OPERATION

Getting Started 3

Basic Software Navigation 3

The Windows XP Environment 3

Using the ODES Software 3

Home (Start-Up) Screen 4

Administration Menu 5

Clinic Information 6

Practitioner Information 6

Environment Settings 7

Data Acquisition Channel 7

Device Settings 7

Global Settings 8

URFIO Configuration Application 8

User Manager 9

Import, Export, and Archive Data 10

Job Demand Templates 11

Superficial Tenderness Reports 11

Protocol Hibernation 12

Remove Current Case 12

Taskbar 13

File Drop-Down Menu 13

Database Utilities 13

Compact and Repair Database 13

Back Up Database 13

Restore Database 14

Log Off and Exit 14

Calibration Drop-Down Menu 14

Statistics Drop-Down Menu 14

Employer Information 14

Patient Status Information 14

Patient Information 15

Referral Information 15

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Insurance Information 15

Statistical Queries 15

Real Time Analysis 15

Export Cervical Data 16

Export Admin Information 16

Import Admin Information 17

Snapshots 17

Creating a Snapshot 18

Emailing, Saving, Removing, and Viewing a Snapshot 18

Forms Drop-Down Menu 18

Utilities Drop-Down Menu 18

Standing/Sitting Tolerance Report 18

Calculators Drop-Down Menu 18

Calculator 18

Deviation Calculator 18

Digital Capture 18

Help Drop-Down Menu 19

Help Manuals 19

About 19

section 02

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40040005 rev. 000

GENERAL OPERATION

I. GETTING STARTED

Ensure that you have carefully read Section 1 of this manual prior to starting up your MCU™.

IMPORTANT

Voltages over 125V can result in eventual damage to the MCU™ electronics and produce

frequent error messages. Even if you have a dedicated circuit for your MCU™, have a tech-

nician check the outlet with a voltmeter to ensure that the wall voltage does not exceed

125 Volts (U.S. and Canada). If your wall voltage exceeds this voltage, call BTE Technolo-

gies immediately.

Damage to your MCU™ resulting from wall voltages exceeding 125 Volts is not covered un-

der the warranty.

Step 1. After making sure everything is plugged in properly, turn on the computer.

Step 2. Once the system is booted and the MCU™ is ready to use, click on the Start Button

and select BTE URFIO Config. The URFIO Config screen will appear for 5 seconds and then dis-

appear; however, it is still running in the background. Refer to Section IV-C on how to access

the URFIO Config screen through ODES.

Step 3. Open the software by double-clicking the ODES icon, which is located on the “desk-

top” of the computer monitor.

II. BASIC SOFTWARE NAVIGATION

The BTE Technologies MCU™ is controlled through its own unique software. Use this section as

both an initial primer and a to-the-point, quick reference guide to your ODES software.

A. THE WINDOWS XP ENVIRONMENT

As a new user of MCU™, it is important for you to first acclimate yourself to the Microsoft

Windows XP operating system.

Familiarize yourself with these basic functions:

Desktop – Once Windows loads up, the entire screen is taken up by the ‘desktop’.

Double-clicking the ODES ‘shortcut’ icon, which is located on the desktop, launches the

ODES software.

Minimize – Clicking this button ‘hides’ the open program and

reduces it to a button on the start bar (Figure 2-1).

Maximize/Restore – Expands the program window to fit the

size of the entire screen. If the program is already expanded,

clicking this will shrink the screen to a smaller window (Fig-

ure 2-1).

Close – Closes the active program window (Figure 2-1).

Scrollbars – Click the small black “up” and “down” arrows on the bar at the right of a

given window to scroll up and down in screens.

Start bar - This horizontal bar located at the bottom of your screen displays a button of

every open program. Clicking a program name here switches you to that program.

Start button – This button is used to launch nearly every program and

function of Microsoft Windows (Figure 2-2).

Figure 2-2.

Start Icon

Minimize

Maximize

Figure 2-1. Minimize/

Maximize/Close

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40040005 rev. 000

B. USING THE ODES SOFTWARE

Once you are comfortable with Windows XP, take some time to familiarize yourself with the

general layout and functioning of the ODES software. Doing this now will maximize your ef-

ficiency down the line.

To access ODES, click on the ODES icon, which is displayed on the computer’s desktop. You

will be prompted for a username and password (Figure 2-3). The username is odes and the

password is bte (both lower case); the username and password may be modified through

the Administration Menu if you choose to do so later.

Upon entering ODES, you will notice the following elements are used throughout:

Title Bar – The narrow blue strip located at the top of the screen which displays the data-

base into which the data is being stored.

Taskbar – Located at the top of the screen under the title bar; while in the home screen,

this bar includes the menus: File, Calibration, Statistics, Snapshots, Forms, Utilities, Cal-

culators, Digital Capture, Patient Standing and Sitting icons, and Help. This bar changes

depending on which area of the software you are using.

Taskbar items – Items listed under each menu title which allow you to perform an opera-

tion or to pull up a report.

Text fields – Text and numerical values are entered into “fields”. To enter text or an in-

teger into a field, click the field, and a blinking black cursor will indicate that the field is

active. Type in the required information.

Check boxes – A checkbox is like a switch; click one to activate a setting and click it again

to de-activate the setting.

Drop-down menu – A text field with an arrowhead pointing down. When the arrowhead is

clicked, the menu drops down to show a list of options available.

III. HOME (START-UP) SCREEN

The first active screen you will see when the ODES program is initiated is the Home Screen (Fig-

ure 2-4). From this screen, all of the settings, patient information, and protocols may be ac-

cessed.

Figure 2-3. ODES Username and Password

Note that the sections on Self Reports, ROM Tests, Strength Tests, and Exercise Program are

covered in this manual; however, these sections are also comprehensively covered in the train-

ing program on The Melbourne Protocol. Refer to Section 10 for more information on this training

program.

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IV. ADMINISTRATION MENU

From the Administration Menu you can control several types of settings, templates, and proto-

cols as well as remove cases (Figure 2-5).

A. History – Patient History Templates

B. Examination – Patient Examination Re-

sults Templates

C. Diagnosis – Patient Diagnosis Templates

D. X-Rays/Lab – Patient X-Ray and Lab Re-

sults Templates

E. Referral – Patient Referral Letter Tem-

plates

F. Impairment – Patient Impairment and

Disability Templates

G. Return To Work – Patient Return To Work

(RTW) Letter Templates

H. Custom Note – Blank Template for Cus-

tomized Notes

I. Progress Analysis – Patient Progress

Analysis Templates

J. Validity Analysis – Comparison of Actual

Results vs. Expected Results

K. Job Demands – Comparison of Job De-

mand vs. Ability Demonstrated

L. Self Reports – Patient-Filled Question-

naires

M. Cardio – Cardiovascular Measurement

Protocols

N. ROM Tests – Range of Motion Protocols

O. Strength Tests – Muscular Strength Pro-

tocols

P. Work Sim Tests – Work Simulation Proto-

cols

Q. Clinical Tests – Clinical Analysis of Pain

Protocols

R. Impairment Ratings – Patient Impairment

Ratings

S. Testing Analysis – Analysis of the Test

Results Templates

T. Recommendations – Recommendation

Letter Templates

U. Cover Letter – Cover Letter Templates

V. Exercise Program – Pre-programmed Ex-

ercises to add to a case

W. Client Information – Create and find cli-

ents and cases; display the current client

X. Reports – Create, edit, and print reports

Y. Exit – Exit the ODES software

Z. Administration – Clinic and Practitioner

Personalization Settings, Software Settings,

Heart Rate Comments, and Protocol Settings

W X Y Z

Figure 2-4. ODES Home Screen

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A. CLINIC INFORMATION

This screen allows you to personalize the reports with your clinic’s information and logo

Figure 2-6).

Add a clinic by clicking New.

To enter a clinic logo, double click

on the Clinic Logo blank field.

Locate the saved logo file on your

hard drive.

The logo can be in any graphic file

format (.jpg, .gif, etc.) and should

be 3.2” x 0.8”, so that it doesn’t

become distorted when attached to

a report.

Edit a clinic’s information by pull-

ing up the clinic’s screen, modify-

ing the necessary information, and

then clicking New, Previous, Next,

or Close.

Remove a clinic by clicking Remove.

Change the default clinic by clicking Next or Previous to select the correct location and

then checking the ‘Set as default clinic’ box. Note that a default clinic cannot be removed

until another clinic has been assigned as the default.

When a report is printed, the default clinic and logo are included on the report.

B. PRACTITIONER INFORMATION

This screen allows you to personalize the reports with the practitioner’s name and digital

signature (Figure 2-7).

Figure 2-6. Clinic Information

Figure 2-5. Administration Menu

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40040005 rev. 000

Step 1. Type in the name and demographics of the

practitioner.

Step 2. To add a digital signature, you must first

scan the signature and save it to your hard drive in

a graphic file format (.jpg, .gif, etc.).

Click the ’allow digital signature‘ box, enter a pass-

word (optional), and double click the icon in order to

locate the signature file on your hard drive.

Step 3. Click Add to include the practitioner to the

database. The name will now appear at the bottom

of the screen.

Edit the health practitioner information by highlight-

ing the name from the list and then clicking Edit. A

practitioner may also be replaced by another within

the Edit screen. Once the changes have been made

click on Add.

Remove the health practitioner information by

highlighting the name from the list and then clicking

Remove.

C. ENVIRONMENT SETTINGS

This screen allows you to set up communication between your wireless hub and computer,

change how you interface with the software, set up reminders, and monitor the wireless

configurations (Figure 2-8).

1. DATA ACQUISITION CHANNEL

Click Auto to ensure the wireless hub is communicat-

ing properly with the computer (Figure 2-9). If there is a

problem, an error message will appear stating that ODES

cannot communicate. Otherwise, if everything is working

properly, a message will appear stating the data acquisi-

tion box has been set up successfully.

Figure 2-7. Health Practitioner

Figure 2-8. Environment Settings

Figure 2-9. DAQ Channel

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2. DEVICE SETTINGS

The Device Settings section indicates which channel the

various tools are being read from based on the set-up of

the software (Figure 2-10). This section is most helpful for

troubleshooting.

3. GLOBAL SETTINGS (FIGURE 2-11)

Country, Units, and Language – Specify the country, language, and the units of mea-

surement to be used in printed reports.

Backup Reminder – Set reminders for backing-up your data. The recommended amount

of time between back-ups is 7 days. The backups should be saved on floppy disks, CDs,

or ZIP disks and kept separate from your system in case of fire, theft, or other equally

damaging events.

Verify or Calibrate – Set reminders for calibrating and verifying the equipment. The rec-

ommended amount of time between calibrations is 7 days, and the unit should be veri-

fied before each day of testing to ensure your tools are accurate. The accuracy of your

equipment is extremely important, particularly if your reports will be used in litigious

cases. In addition, the Reminder can be set up as ‘Remind only’ or ‘Must Be Done’.

Spell Checker – Spell check your documents using Microsoft Word or the provided Medi-

cal Spellchecker.

Automatically Read Shelf Heights – This is not used for an MCU™ system.

Voice Type – Change the type and speed of the voice interface. You may also turn the

sounds and voices on and off by clicking on the knobs.

4. URFIO CONFIGURATION APPLICATION

The URFIO Configuration Application is the portion of the software that monitors the

wireless configurations of the system (Figure 2-12).

Clicking on the URFIO Configurator icon brings up the URFIO Configuration Tool Mapping

screen (Figure 2-13). This screen displays which wireless channel the system is operat-

ing on and which tool is mapped to that current wireless channel. This screen should

only be used when a new tool needs to be mapped or for troubleshooting purposes.

Figure 2-11. Global Settings

Figure 2-12. DAQ Channel

Figure 2-10. Device Settings

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40040005 rev. 000

If a tool needs to be mapped: click on the tool name under Tool Selection, highlight the

tool’s serial number under Available Tools, and then click the green arrow to map the

tool; the serial number should appear under Current Mapping. To unmap a tool, click on

the tool name under Tool Selection (the serial number must appear under Current Map-

ping), click on the red arrow; “Not Mapped” should appear under Current Mapping.

D. USER MANAGER

This screen allows you to add, edit, and remove users as well as set each user’s level of

rights to the software (Figure 2-14).

To add a new user, enter a user’s name, password (case sensitive), and select a security

level from the drop-down menu. Click Add to include the new user.

When the user signs into the software, he or she will use the name and password assigned

in this screen.

Edit a user’s information by highlighting their name on the right hand side of the screen

and clicking on Edit. Once the changes have been made, click on Update.

Delete a user by highlighting their name and then clicking on Remove.

Descriptions of the security levels:

Administrator – All rights

High – All rights except User Manager

Medium High - All rights except User Manager and removal of cases

Medium - All rights except Administration

Low Medium - All rights except Administration, Reports, removal of assigned protocols

to a client, and deletion of tests

Figure 2-13. URFIO Configuration Tool Mapping

Figure 2-14. User Manager

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Low - All rights except access to client notes, Administration, Reports, and unable to

edit, delete or create tests

Lowest - Only access to client information and client case information

E. IMPORT, EXPORT & ARCHIVE DATA

This screen allows you to import and export data with varying degrees of detail (Figure 2-

15).

Step 1. Click Browse to locate the data-

base you wish to import or export the data

from. Highlight the desired database and

click Open. The database information will

be now listed. You will be prompted to in-

clude the ODES Database Password if you

are importing or exporting from an ODES

database that is in a zipped format.

Note that the imported/exported database

cannot share the same name as an exist-

ing database. Rename the file and try

again.

Step 2. Select whether you would like to import to your current database or export data

from your current database to another.

Step 3. Select the Client Import Criteria:

All Clients – import/export all clients; new templates, custom tests, and super proto-

cols are imported/exported as well

Selected Clients – import/export select clients; new templates, custom tests, and su-

per protocols are imported/exported as well

Starting Date – import/export according to clients’ start date; new templates, custom

tests, and super protocols are imported/exported as well

Status – import/export according to clients’ status; new templates, custom tests, and

super protocols are imported/exported as well

Employer – import/export according to clients’ employer; new templates, custom tests,

and super protocols are imported/exported as well

No Clients – import/export only new templates, custom tests, and super protocols

Step 4. Choose how you would like the data handled by clicking on the boxes next to the

options.

Step 5. Once all of the parameters are set to your preferences, click Start.

Note that when an import/export is processed, the software will run a check of the tests.

If any changes have been made to the standard tests, the software considers this as a new

test and will include copies of both. You may wish to store the duplicates under protocol hi-

bernation or delete them. However, be aware that deleting a test also deletes the data from

that test in all patients’ files.

It is recommended that if you will be importing data obtained off-site to your main database,

you should export the main database (no clients) to the local database you will be using.

Therefore, when you import the data from your local database back to the main database,

there will be no test duplicates since the software recognizes these as the same databases.

Figure 2-15. Import/Export & Archive Data

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A progress screen will appear and then a notification will indicate whether the import/ex-

port was successful or not.

F. JOB DEMAND TEMPLATES

This screen allows you to create, edit, delete, and print Job Demand Templates (Figure

2-16). These templates can be used within the Job Demands screen that is accessed from

the Home Screen.

Add a new Job Demand Template by clicking New. Enter the job title and source of the in-

formation (I.e. Job Site Analysis, Dictionary of Occupational Titles, Self Report, etc.).

The Section Header is optional; however, if Section Headers are used, the Job Demand

Templates will be grouped by Section Header (I.e. lifting, positional tolerance, mobility,

etc.) whenever the templates are printed.

Include details on job tasks, units of measurement, and the job demand level (OCCasional

– 1-33%; FREQuent – 34-66%; CONstant – 67-100%). Click Save once you have added all

the needed information.

Import templates by clicking Import and selecting the directory from which you will be

retrieving the templates and the directory into which you will be importing the templates.

You must also indicate whether you will be importing all the templates in the source ODES

database or just the current template.

Print the Job Demands Templates by clicking Print. The report can also be printed by click-

ing Export to create the report as a Word document (if you have Microsoft Office installed

on your computer), or by creating a report Snapshot (see the Snapshot section of this

manual).

Edit a Job Demand Template by selecting the job from the drop-down menu, clicking Edit,

and making any required changes.

Remove a Job Demand Template by selecting the job from the drop-down menu and click-

ing Remove.

Access a Job Demands Template within the Job Demands screen by selecting the job from

the drop-down menu and clicking Populate. This will add the header, job task, job demand

level, units, and information source to the appropriate fields. Complete the Ability Demon-

strated fields, and determine whether there is a job match or not.

Add a Job Demand template from the Job Demands screen by clicking on Add to Template.

G. SUPERFICIAL TENDERNESS REPORTS

This screen allows you to create, edit, and delete Superficial Tenderness Templates. These

templates can be accessed through the Superficial Tenderness protocol within the Self

Reports screen (Figure 2-17).

Figure 2-16. Job Demand Templates

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Add a new template by clicking New.

Edit an existing template by clicking Edit and then selecting the template.

Remove an existing template by clicking Remove and then selecting the template.

H. PROTOCOL HIBERNATION

This screen allows you to place protocols, which may not be used often, in hibernation

as well as remove protocols, which may be needed, from hibernation. Moving protocols in

and out of hibernation does not delete the data or testing information. Note that protocol

hibernation can also be accessed through the protocol pages (Figure 2-18).

Hibernate a test by highlighting the test on the left hand side of the screen and then click-

ing Put into Hibernation. The test should now appear on the right screen and not the left

one.

Bring a protocol out of hibernation by highlighting the test from the right hand side of the

screen and then clicking Awaken From Hibernation. The test should now appear on the

left screen and not the right one.

I. REMOVE CURRENT CASE

This screen allows you to delete the client case that has been selected from within the home

screen. Note that once a case has been deleted, it cannot be retrieved.

Step 1. Remove the current client case by clicking Remove Current Case.

Figure 2-17. Superficial Tenderness Templates

Figure 2-18. Protocol Hibernation

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Step 2. A warning will appear prior to deleting data. Click Yes to remove the case.

V. TASKBAR (FIGURE 2-19)

A. FILE DROP-DOWN MENU

1. DATABASE UTILITIES

This screen allows you to open a database, create a new database, rename an existing

database, and remove an existing database (Figure 2-20).

Open a database by locat-

ing the database, double

clicking the name in the

Search Results field, and

then clicking Open. After

confirming that you would

like to open the database

selected, the home screen

will appear with the se-

lected database available

to use. The blue title bar

at the top of the screen

should now read the

opened database.

Create a new database by typing in the new database name within the Database Loca-

tion text field, clicking Use Blank, and then confirming you would like to create this new

database.

Rename an existing database by locating the database you would like to change, double

clicking the name in the Search Results field, modifying the name within the Database

Location text field, clicking Rename, and then confirming you would like to rename this

database.

Remove a database by double clicking the name in the Search Results field, clicking

Remove, and then confirming you would like to delete this database.

Note that once a database has been removed, it can not be recovered by you or BTE

Technologies.

2. COMPACT & REPAIR DATABASE

This screen allows you to repair any small errors that

may occur due to networking (Figure 2-21).

Repair the database by clicking on Compact & Repair.

A screen will pop up confirming you would like to repair

the database currently in use.

Another screen will appear once the repair is successful.

3. BACK UP DATABASE

This screen allows you to back up your databases; this is highly recommended in the

case your hard drive becomes irrecoverable and you cannot access your files (Figure 2-

22).

It is recommended that you compact and repair your database every one to two months.

Figure 2-19. ODES Taskbar

Figure 2-20. Database Utilities

Figure 2-21. Compact &

Repair Database Message

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Back up a database by locating the directory you

would like to save the database to, selecting whether

or not to use a password, selecting whether or not to

back up the impairment ratings, selecting whether or

not to erase the disk, and then clicking Start Back

up.

Note that BTE Technologies cannot recover any lost or

forgotten passwords that have been used for back ups.

4. RESTORE DATABASE

This screen allows you to restore a previously backed up database (Figure 2-23).

Restore a database by locating the

directory you would like to restore

the database from, entering the

password if necessary, selecting

whether to keep the original name

or not, selecting whether to restore

the impairment ratings or not, and

then clicking Start Restore.

Note that if you choose to restore with a name that is the same as another database,

the other database will be overwritten by this new restore.

After you restore a database, you must use the Database Location field to find the

newly restored database.

5. LOG OFF AND EXIT

The Log Off option is to be used if you are going to be using ODES on and off throughout

the day. By logging off rather than exiting, the speed of ODES will be enhanced.

It is recommended you exit the program at the end of each day and shut down the com-

puter.

B. CALIBRATION DROP-DOWN MENU

This section is covered in Section 5 - Calibration & Verification.

C. STATISTICS DROP-DOWN MENU

1. EMPLOYER INFORMATION

Provides a summary of all Employers that are stored within the Case Information section

of the ODES database. The report can be printed, exported to a snapshot file format, or

exported to Microsoft Word (if Word is installed on the computer).

2. PATIENT STATUS INFORMATION

Provides a summary of all Client Statuses. If the status of a client has been added to

the database in the Client Case page, the client will be added to this report. You may

sort by last name or by the status of the client. The report can be printed, exported to

a snapshot file format, or exported to Microsoft Word (if Word is installed on the com-

It is highly recommended that you back up your database to a floppy disk, CD, or ZIP

disk at the end of each day. A back-up reminder can be set within the Environment

Settings Screen.

If you are using a laptop or will be transporting your computer, we recommend back-

ing up your database prior to moving the system.

Figure 2-22. Back Up Database

Figure 2-23. Restore Database

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puter).

3. PATIENT INFORMATION

Provides a summary of all client information that has been added to the database. The

report can be printed, exported to a snapshot file format, or exported to Microsoft Word

(if Word is installed on the computer).

4. REFERRAL INFORMATION

Provides a summary of all referral sources that have been entered into the database.

The report can be printed, exported to a snapshot file format, or exported to Microsoft

Word (if Word is installed on the computer).

5. INSURANCE INFORMATION

Provides a summary of all insurance companies that have been entered into the da-

tabase. The report can be printed, exported to a snapshot file format, or exported to

Microsoft Word (if Word is installed on the computer).

6. STATISTICAL QUERIES

Allows you to query for information regarding existing clients by searching various crite-

ria (Figure 2-24):

•Case Manager

•Employer

•Physician

•Attorney

•Referral Source

•Insurance Company

•Supervising Practitioner

•Status

•Pre/Post off of employment

•Start/End Date

•Injury Locations

The report provides detailed informa-

tion on length of treatment, common

injuries, and the number of clients be-

ing referred from a specific source.

Under report type, select ‘Detailed’ to

obtain a list of the clients, and select

‘No Details’ to obtain the summary

without client names.

The report can be printed, exported to a snapshot file format, or exported to Microsoft

Word (if Word is installed on the computer).

7. REAL TIME ANALYSIS

Allows you to analyze the data from each individual client in detail. It also allows you to

compare individual or multiple trials of any strength test that is recorded in the data-

base. Real Time Analysis is useful for research, analyzing job demands, and client prog-

ress/tracking (Figure 2-25).

Step 1. Select the protocol to analyze.

Step 2. Select the test range.

Figure 2-24. Statistical Queries

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Step 3. Specify whether you wish

to analyze a specific trial or the

average of the trials relating to the

specific protocol for a specific cli-

ent.

Step 4. Specify which position you

would like to graph.

Step 5. Indicate the time frame

you would like to analyze (option-

al).

Step 6. Click Analyze and a graph

of the real time analysis will ap-

pear.

8. EXPORT CERVICAL DATA

Allows Multi-Cervical users participating in International research with the Melbourne

Protocol to export raw data into a program outside of ODES. This allows the user to work

with the data in a spreadsheet format if so desired (Figure 2-26).

Step 1. Select the type of testing

data you wish to export.

Step 2. Select the fields you wish to

include when exporting.

Step 3. Specify your target popula-

tion (including client status, gender,

and age range) or target dates.

Step 4. Select a file name and a

directory – your data will be saved

as a text file here.

The file name that you chose will

now be written in the ‘File Name to

Export Into’ line.

A confirmation message will appear

once the export is successful.

In order to locate the exported data,

close ODES and return to the Win-

dows Desktop. Open the program

into which the data was exported

(e.g. Excel). Click on the Data tab,

select Import External Data and

then Import Data. Locate the text file

which was just exported, open the

file, and follow the directions given.

The exported data should now appear

in the spreadsheet.

9. EXPORT ADMIN INFORMATION

Allows you to export the administrative information related to the various protocols, su-

per protocols, and templates (Figure 2-27).

Figure 2-25. Real TIme Analysis

Figure 2-26. Export Cervical Data

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Step 1. Select which protocols, super protocols, or templates you would like to export.

Step 2. Click Browse to find the directory you would like to export into.

Step 3. Enter a password (optional) and click Start Export.

10. IMPORT ADMIN INFORMATION

Allows you to import the administrative information related to the various protocols,

super protocols, and templates (Figure 2-28).

Step 1. Locate the directory you would like to import from.

Step 2. Enter the password if needed and click Start Restore.

D. SNAPSHOTS

This screen allows you to create PDF-like files from reports so that they may be emailed

without compromising the validity of the document (Figure 2-29). A snapshot viewer ex-

ecutable file is bundled with the report file, which will allow individuals without ODES (e.g.

insurance companies and manufacturing plants) to view the reports.

Figure 2-27. Export Administration Information

Figure 2-28. Import Administration Information

Figure 2-29. Report Snapshot Viewer

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1. CREATING A SNAPSHOT

Step 1. Click on Reports within the Home Screen.

Step 2. Preview the report you would like to snapshot.

Step 3. Within the taskbar, select Export then Create a Report Snapshot.

The report will now be exported into a report snapshot, and a message will appear once

the save is successful.

2. EMAILING, SAVING, REMOVING, AND VIEWING A SNAPSHOT

Step 1. From the Home Screen taskbar, click on Snapshots.

Step 2. Locate the snapshot you wish use. Double click on the file name within the

Search Results field, and the file name should appear within the Report Snapshot text

field.

Step 3. Click on whichever operation (Email, To Floppy, Remove, or View) you would

like to perform.

If you choose to email the snapshot, a message will appear asking if you would like to

include the snapshot viewer. If the email recipient does not have ODES or has never

viewed a snapshot before, you must email the viewer. Make sure the recipient is aware

that the viewer is included with the email and it must be used to view the report.

E. FORMS DROP-DOWN MENU

This menu offers a variety of questionnaires and forms available for printing. The client

can fill out these forms and the information can be entered manually into the software.

F. UTILITIES DROP-DOWN MENU

1. STANDING/SITTING TOLERANCE REPORT

Using the standing and sitting icons within the taskbar, you can track a client’s toler-

ance of standing and sitting and with respective to time (Figure 2-30).

Click on either the standing or the sitting icon to begin the

timer. Once the client can no longer tolerate the chosen op-

tion, click Stop.

The Standing/Sitting Tolerance Report tabulates the date and time started, the position

of the client, the duration of time the client was able to stand or sit, the total amount of

time standing or sitting, and the percentage of total standing vs. total sitting. Note that

the duration of time is rounded to the closest minute.

G. CALCULATORS DROP-DOWN MENU

1. CALCULATOR

Calculator for basic arithmetic needs

2. DEVIATION CALCULATOR

Calculator for finding the standard deviation of at least two values

H. DIGITAL CAPTURE

This screen allows you to insert a variety of pictures with accompanying headings and com-

ments. This feature is useful for showing clients how to perform tasks or exercises (Figure

2-31).

Figure 2-30. Standing/

Sitting Tolerance

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Step 1. Take the picture with a digital camera.

Step 2. Download the picture to your hard drive using your camera software.

Step 3. Within the Digital Capture Observations screen, click on the binoculars icon to

locate the picture in the directory it was saved and click Open.

Step 4. Click Insert and the picture should appear in the large box.

Step 5. Enter a picture title and any comments if desired. The comments are included

when a page of pictures is printed.

Step 6. A picture may be removed by clicking Remove below the file name text field.

Step 7. An entire page of pictures may be printed, deleted, and created by using the Print,

Delete, and New icons at the top of the screen.

I. HELP DROP-DOWN MENU

1. HELP MANUALS

A PDF version of this MCU™ manual is located here. If you have loaded the Adobe

Acrobat Reader and the help manuals onto your hard drive, you will be able to access

the manuals directly. However, if you have no loaded software and manuals, you will be

prompted to insert the ODES CD in your disk drive. You can load Adobe Acrobat Reader

for free at www.adobe.com.

2. ABOUT

A screen showing the attributes of your specific MCU™ and ODES software. This is a

helpful screen to view whenever you need to call customer service.

Figure 2-31. Digital Capture

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03 - CLIENT INFORMATION

Introduction 3

Adding a Client 3

Adding a Case 4

Adding a Family Physician/Specialist/Attorney/

Referral Source/Insurance Company/Employer 4

Adding Current Medications 4

Client Photos 4

Client Status 5

Start/End Time 5

Evaluator 1 and 2 5

Adding in ICD-9 Codes 5

Areas of Complaint 5

Locking Cases 5

Finding a Client/Case 6

Adding and Removing Tests 6

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CLIENT INFORMATION

I. INTRODUCTION

The client information screen can be accessed from the center of the home screen, just above

the client drop-down menu (Figure 3-1).

ADDING A CLIENT

In order to utilize the software, a client must first be entered. It is recommended to start by

creating a sample client in order to get familiarized with the software without having to worry

about losing valuable information (Figure 3-2).

Step 1. Click on Client Information within the Home Screen.

The Client Information screen will appear.

Step 2. Click on New Client.

Step 3. Enter all the demographics of the client.

The required information includes the name, gender, birth date, and dominant hand. This data

is required for tests which compare the client’s objective measurements with a normative data-

base.

Step 4. Click Close once all the information is entered.

The client is now stored in the database and should appear in the drop-down menu within the

Client Information screen.

Figure 3-1. Client Information Icon

Figure 3-2. Client Information

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III. ADDING A CASE

All clients must have a case associated with their file.

Within the Client Information screen, click New Case.

The Client Case Information screen allows you to enter information regarding the client’s physi-

cian, medications, referral sources, employment, insurance, ICD-9 codes, etc. (Figure 3-3).

A. ADDING A FAMILY PHYSICIAN/SPECIALIST/ATTORNEY/REFERRAL SOURCE/INSUR-

ANCE COMPANY/EMPLOYER

Enter a new contact by double clicking on the white text box. A new window will appear that

allows you to add in the contact information. After entering in the information and closing

the new window, the contact’s name will appear in the drop-down menu for that particular

contact type. This data will be saved in your database so the information will only have to

be entered once.

B. ADDING CURRENT MEDICATIONS

A list of client medications can be added by double clicking in the white text box. The

Current Medications screen will appear and this allows you to enter in the name of the

medication as well as a description of its purpose and usage. If the client is taking a

medication that has previously been entered, select the name of the medication from

the drop-down menu and enter the remaining information by either typing it in or select-

ing it from a drop-down menu. Once all the information has been added, and the screen

is closed, the Current Medications text box will be populated with all of the medication

names.

C. CLIENT PHOTOS

This screen gives you the ability to add a client’s picture into his or her file, and this in

turn will be incorporated into that client’s reports. You must first take a picture with a

digital camera and then save the picture to your hard drive. Once that is done, click on the

large white box in the upper right hand corner of the Client Case page or click on Picture

at the bottom right hand corner of the page. Click Browse to locate the picture and then

Figure 3-3. Case Information

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click Insert to add the photo.

D. CLIENT STATUS

The client status field is useful for keeping track of the amount and type of assessments

you have completed. Client status can also be used as a criterion under Statistical Que-

ries. The drop-down menu should already be populated with status options, but you can

also add, edit or remove status information by double clicking on the blank text field.

E. START/END TIME

The assessment start time and date are automatically logged on the Client Case page when

you click on New Case in the Client Information Screen. In order to record an end time,

simply double click in the corresponding blank field once the assessment is completed,

and the current time will be entered into the field. You may also manually enter a time by

typing in the text field. The evaluation times will be displayed on the cover sheet of your

report.

F. EVALUATOR 1 AND 2

The Evaluator 1 and 2 fields allow the evaluator(s) to enter their name and credentials

into the Client Case page. Enter a new Evaluator by double clicking in text field. A screen

will pop up which will allow you to enter in the Evaluator’s name, designation, occupation

and registration number. This information will be included in the front of the report and

beneath the signature sign-off line (if a signature is requested when printing the report).

Please note this is not a feature of all reports printed in ODES. Click the Allow Digital

Signature checkbox if you would like to add your signature to the software; this is a useful

tool if you are anticipating e-mailing reports. See Section 2-IV-B on directions for adding a

digital signature.

G. ADDING IN ICD-9 CODES

ICD-9 codes can be stored within ODES for later use. Double click the blank ICD-9 Codes

box on the Client Case page, and a screen will pop up allowing you to select the proper

codes. To assign an existing ICD-9 code to your client, select the code from the Codes in

Database drop-down menu and click Add. Create new codes by double clicking on the ICD-9

Codes in Database field and entering in the code and description. Once an ICD-9 code has

been added to the database, it will be available from the drop-down menu for future cli-

ents. In addition, once a code is entered, it is available for use in the note templates.

H. AREAS OF COMPLAINT

A client’s areas of complaint may be obtained from his or her responses to the Pain Dia-

gram or the Ransford Pain Diagram. To enter the information into the database, double

click on the large Area of Complaint Information box or click Add in the Area of Complaint

Information section of the Client Case page. A pain diagram will be displayed, which will

allow you to enter in location information and pain descriptions. After clicking on the dia-

gram location where the client presents a complaint, complete the chart that is below the

body diagrams. Once you have entered all the information, click Add, and it will appear on

the Client Case page.

I. LOCKING CASES

This feature allows the evaluator to prevent other individuals from modifying a case. In

order to access a locked case, a password must be entered. Please note that it is your

responsibility to remember this password. If the password is forgotten, our technical sup-

port/customer service staff at BTE Technologies, Inc. will not be able to help you retrieve

it. Lock the case by clicking Lock Case at the bottom of the Client Case page. A screen will

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appear prompting you to enter and confirm a password. Click OK when you are done. Once

locked, you will see the Lock Case icon change to Unlock Case.

Once the Client Case page is complete, you may click the Close button located at the bottom

right hand corner of the page; this will bring you back to the Client Information page, and a

case number will now be associated with your client. Click the Close button in order to return

to the Home Screen. The new client will now be listed in the drop-down menu underneath the

Client Information button. To quickly access a client’s information screen, double click on the

client’s name. You can also quickly access the client’s case information by double clicking on

the case number under the client name drop-down menu.

III. FINDING A CLIENT/CASE

ODES allows you to search for a client or case

using various probes. Within the Client Infor-

mation screen, click on Find a Client or Find a

Case to access these options (Figure 3-4).

You may search using any of the fields. Remem-

ber that the more fields which are selected, the

narrower the search. If you’re having trouble

finding a case or a client, try selecting only one

or two fields to broaden the search.

Once you have populated the fields you wish to

search by, click on the binoculars icon to re-

trieve the search results.

Open a client or case file by clicking on the

arrow button to the left of the name or case

number.

IV. ADDING AND REMOVING TESTS

Once you had added your client into ODES you can assign tests to the client.

From the Home Screen, click on Self Reports, Cardio, ROM Tests, Strength Tests, Work Sim

Tests, or Clinical Tests. The same basic screen appears for each icon: the box on the left lists

the tests related to the icon you selected, and the box on the right lists all the tests assigned

to the client (Figure 3-5).

Figure 3-4. Find a Client

Figure 3-5. Adding and Removing Tests

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Add a new test to the client by either highlighting the test name in the left box and clicking

Add to Client or by double clicking on the test name in the left box.

Once the test has been assigned to the client it will appear in the right box.

Change the order the tests will be completed in by highlighting the test in the right box and

use the up and down arrows under Change Protocol Order.

Perform the test assigned to a client either by highlighting the test in the right box and click-

ing on Perform Test or by double clicking on the test in the right box.

Remove a test from a client by highlight the test in the right box and clicking Remove From

Client.

You can access the other types of tests without having to go back to the Home Screen ev-

ery time by clicking on the desired test-category box displayed at the bottom of the Protocol

Screen.

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04 - TEMPLATES

Pre-Programmed Templates 3

Custom Templates 4

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TEMPLATES

Each of the Notes pages in ODES has a template section that allows you to create any number of

templates. This feature allows you to specify which client information you would like to include on

each report and in which location. For example, the client’s name, date of injury, and injury loca-

tions could be inserted in the upper left hand corner of a report. This feature speeds up reporting

time, improves efficiency, and hence, profitability.

You can find pre-programmed templates or create your own templates within the following Home

Screen categories:

•History •X-Rays/Lab •Return to Work

•Testing Analysis •Examination •Referral

•Custom Note •Recommendations •Diagnosis

•Impairment •Progress Analysis •Cover Letter

I. PRE-PROGRAMMED TEMPLATES

To access the pre-programmed templates, click on one of the categories listed on the left side

of the Home Screen. Click on the template icon in the lower right hand corner of the screen

(Figure 4-1).

This will bring you to the main Templates screen (Figure 4-2).

Step 1. To view or edit a template, first click on Edit; the Edit icon should change to Cancel

Edit. Next click on the pre-programmed template you wish to use.

A screen will appear with the generic template code (Figure 4-3).

Step 2. Highlight the code and either press CTRL-C on your keyboard or pull down the Edit

menu in the taskbar and select Copy. This will copy the code to your clipboard.

Step 3. Click the Close icon within the pre-programmed template’s screen. This will return you

to the main Templates screen.

Figure 4-1. Template Icon

Figure 4-2. Main Templates Screen

Figure 4-3. Generic Template Code

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Step 4. Click Cancel Edit and then select the template you just viewed. This will bring you to

the corresponding screen (Figure 4-4).

Step 5. While in the home template screen, click within the white text box to place the cursor

and paste in the code. You can paste by either pressing CTRL-V on your keyboard, clicking on

the Paste icon within the home template screen, or pulling down the Edit menu in the taskbar

selecting Paste (Figure 4-5).

The code will be updated with the client’s information, but you must still populate the fields

with carets and select which bracketed options apply.

Note that any client demographics within brackets – [ ] – will automatically be populated with

the client’s information that has been entered in the client information and case screens (i.e.

title, name, gender). All other information which is bracketed but isn’t available from these

screens will remain intact until deleted. This is typically used when there are several options

to describe the situation and you must pick the most applicable one (i.e. condition is either

controlled by medication, in remission, or has resolved itself). Any text within carets – << >>

– is intended to alert the evaluator to fill in the information (i.e. name of the condition and

year of the diagnosis).

Edit a pre-programmed template by clicking Edit in the main Templates screen and selecting

the template you wish to modify. You can then add fields by selecting the desired field from the

Insert Field drop down menu and clicking Insert or delete fields using the delete key on your

keyboard. The text may also be modified as you see fit.

To delete any template, first click the Delete icon in the main Templates screen; the Delete

icon should change to Cancel Delete. Next click on the pre-programmed template you wish to

delete.

II. CUSTOM TEMPLATES

To create or access a custom template, click on one of the categories listed on the left side of

the Home Screen. Click on the template icon in the lower right hand corner of the screen (Fig-

ure 4-5).

Figure 4-5. Updated Template Code

Figure 4-6. Template Icon

Figure 4-4. Blank Notes Screen

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This will bring you to the main Templates screen (Figure 4-7).

Step 1. Create a new template by clicking on New. A new icon will appear within the main

Templates screen.

Step 2. To view the template, first click on Edit; the Edit icon should change to Cancel Edit.

Next click on the template you just created.

A screen will appear with a blank text box (Figure 4-8).

Within this screen you can change the name of the template as well as create the generic code

by inserting fields and typing text.

Step 3. Begin by writing what you wish to include in the report, but use the merge fields when

you would like information automatically populated. The software already includes multiple

pre-programmed merge fields which are listed under the Insert Field drop down menu.

Insert a merge field by selecting the field from the Insert Field drop down menu and click-

ing Insert. The merge field will be inserted where the text cursor is located. The merge field

should have brackets – [ ] – around the text.

You may create your own merge fields by typing the options you would like to include and plac-

ing brackets around each one. This is useful when there are several options to describe the

situation and you must pick the most applicable one (i.e. “client arrived [early][on time][late]

for the assessment…”).

You can also include characters which alert you to personalize a field for the client. This is

useful when you need to include information which is different for every client but must be

included in the report (i.e. “client has been diagnosed with <<Enter Diagnosis>> on <<Enter

Date>> by a <<Enter Specialist>>…”). The pre-programmed templates use carets – << >> – to

bring your attention to the field, but you may use any characters you like (Figure 4-9).

Figure 4-7. Main Templates Screen

Figure 4-8. Blank Template

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Step 4. Once you have finished creating the code, highlight the code and either press CTRL-C

on your keyboard or pull down the Edit menu in the taskbar and select Copy. This will copy the

code to your clipboard. Next, click the Close icon within the custom template’s screen. This

will return you to the main Templates screen.

Step 5. Click Cancel Edit and then select the template you just viewed. This will bring you to

the corresponding screen (Figure 4-10).

Step 6. While in the home template screen, click within the white text box to place the cursor

and paste in the code. You can paste by either pressing CTRL-V on your keyboard, clicking on

the Paste icon within the home template screen, or pulling down the Edit menu in the taskbar

and selecting Paste (Figure 4-11).

The code will be updated with the client’s information, but you must still populate the fields

Figure 4-11. Updated Custom Template Code

Figure 4-9. Custom Template Code

Figure 4-10. Blank Notes Screen

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with carets and select which bracketed options apply.

Edit a custom template by clicking Edit in the main Templates screen and selecting the tem-

plate you wish to modify. You can then add fields by selecting the desired field from the Insert

Field drop down menu and clicking Insert or delete fields using the delete key on your key-

board. The text may also be modified as you see fit.

To delete any template, first click the Delete icon in the main Templates screen; the Delete

icon should change to Cancel Delete. Next click on the pre-programmed template you wish to

delete.

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05 - CALIBRATION & VERIFICATION

Introduction 3

Performing the Calibration 3

Performing the Verification 7

Calibration Reports 8

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CALIBRATION & VERIFICATION

I. INTRODUCTION

Calibration is an important component of the Multi-Cervical™ system. Since one of the main

attributes of the system is the ability to track the progress of your patients, it is essential that

the equipment is always giving accurate feedback. Therefore, we recommend calibrating every

7 days and verifying the beginning of every day.

As shown in Section 2 under the Administration Menu overview, reminders may be set for cali-

brations and verifications. There is also an option of requiring that the calibration and verifica-

tion must be done.

II. PERFORMING THE CALIBRATION

Calibration may be performed for the head braces, halo (2 locations), and the seat.

Access the Calibration Screen by selecting Calibrate FOCUS & MCRP from the Calibration

drop-down menu, which is located in the taskbar (Figure 5-1).

The main calibration screen will appear (Figure 5-2). Make sure that under Calibration Type,

which is located in the upper left of the screen, Manual is selected. The calibration screen

also has the Detail On feature, which allows you to directly view the voltage values of any tool

that can be calibrated; this is useful when troubleshooting.

Figure 5-1. Calibration Drop-Down Menu

Figure 5-2. Main Calibration Screen

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Select the Cervical icon from the main calibration screen to bring up the MCU™ calibration

screen (Figure 5-3).

The screen will always indicate the last day of successful calibration in addition to the amount

of weight used for the last calibration.

Step 1. Secure the head brace you wish to calibrate to the calibration plate. Make sure the

RJ45 cable is plugged into the head brace as well to the jack closest to the front of the unit

on the top of the MCU™ (Figure 5-4). Click the first OK on the calibration screen.

Step 2. Place the calibration block on the head brace (Figure 5-5).

Figure 5-3. Cervical Calibration Screen

Figure 5-4. Preparing Head Brace for Calibration

Figure 5-5. Placing Calibration Block on Head Brace

0.7lb

0.3kg

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Step 3. Place the calibration weight(s) on the calibration block (Figure 5-6). Enter the amount

of weight you are using to calibrate (remember to add the weight of the calibration block,

which is 0.7lb/0.3kg) in the calibration screen and then click OK.

Step 4. Remove the calibration weights from the calibration block before proceeding with the

rest of the calibration.

Step 5. If it isn’t already, set the halo rotation to 0 degrees (Figure 5-7). Click OK on the cali-

bration screen.

Step 6. Unlock the rotation pin, set the halo rotation to 90 degrees left, and then lock the

rotation pin (Figure 5-8). Click OK on the calibration screen.

Step 7. Unlock the rotation pin, rotate the halo back to 0 degrees, and then lock the rotation

pin.

Figure 5-6. Calibrating the Head Brace

Figure 5-7. Halo at 0o Rotation

Figure 5-8. Halo at 90o Rotation

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Step 8. If it isn’t already, set the halo flexion/extension angle to 0 degrees and insert the

ROM stop pin (Figure 5-9). Click OK on the calibration screen.

Step 9. Remove the ROM stop pin, set the halo flexion/extension angle to 70 degrees flexion,

and then insert the ROM stop pin (Figure 5-10). Click OK on the calibration screen.

Step 10. Remove the ROM stop pin, set the halo flexion/extension angle back to 0 degrees,

and insert the ROM stop pin.

Step 11. If it isn’t already, lower the seat height to its lowest position (Figure 5-11). Click OK

on the calibration screen.

Figure 5-9. Halo at 0o Flexion/Extension

Figure 5-10. Halo at 70o Flexion

Figure 5-11. Seat Height at Lowest Position

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Step 12. Make sure the seat back is at its lowest position, and then raise the seat height to

its highest position (Figure 5-12). Click OK on the calibration screen.

Step 13. Once the device has been successfully calibrated, a screen will appear requesting

the name of the individual who just completed the calibration.

III. PERFORMING THE VERIFICATION

It is recommended that the accuracy of the device be verified after calibration. In addition,

verification should be completed prior to testing each day or after the equipment has been set

up.

Note that verification may only be performed on the head braces.

The Verification Screen can be accessed under the Calibration menu within the taskbar or

within the individual tool calibration screens (Figure 5-13).

The main verification screen will appear (Figure 5-14).

Figure 5-13. Calibration Drop-Down Menu

Figure 5-14. Main Verification Screen

Figure 5-12. Seat Height at Highest Position

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Select the Cervical icon from the main verification screen to bring up the MCU™ verification

screen (Figure 5-15).

The screen will always indicate the last day of successful verification.

The verification tools and process are the same as calibration. However, you must make sure

to use a different amount of weight for the verification than you did for the calibration.

Lastly, remember to include the weight of the calibration fixture, which is 0.7lb.

Once the device has been successfully verified, a screen will appear requesting the name of

the individual who just completed the calibration. In addition, the verification screen will show

the weight that you entered compared to the weight that the software calculated.

IV. CALIBRATION REPORTS

To print or view the calibration and verification reports, go to the Calibration menu within the

taskbar and then Calibration Reports (Figure 5-16).

You may filter the calibration report according to latest calibration, all calibrations, or date

range (Figure 5-17).

Print a report by clicking Print.

View a report by clicking Print Preview.

Figure 5-15. Cervical Verification Screen

Figure 5-16. Calibration Drop-Down Menu

Figure 5-17. Calibration Report Options Menu

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Reports include the name of the person who performed the calibration/verification, the date

when the calibration/verification occurred, and actual weight vs. measured weight, and any

deviation from the accuracy of the device (Figure 5-18).

Figure 5-18. Calibration and Verification Report

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06 - PROTOCOLS

Self Reports 3

Utilizing Self Reports 3

Editing and Creating Self Reports 4

Cardiovascular Protocols 5

Utilizing Cardiovascular Protocols 5

Editing and Creating Cardiovascular Protocols 5

ROM Protocols 7

Positioning the Patient for a Cervical ROM Protocol 7

Positioning the Patient for a ROM Flexion or Extension Test 8

Positioning the Patient for a ROM L/R Rotation Test 9

Positioning the Patient for a ROM Lateral Flexion Test 10

Utilizing the Cervical ROM Protocol 11

Accessing the Cervical ROM Protocol 11

Utilizing the ROM Flexion Test 13

Utilizing the ROM Rotation Test 14

Utilizing the ROM Lateral Flexion Test 15

Utilizing the ROM Extension Test 17

Strength Protocols 18

Positioning the Patient for a Neutral Cervical

Isometric Strength Protocol 18

Positioning the Patient for an Isometric Flexion/Extension Test 20

Positioning the Patient for an Isometric Lateral Test 21

Positioning the Patient for a 25 Degree Cervical

Isometric Strength Protocol 22

Positioning the Patient for a 25o Isometric Flexion/Extension Test 24

Positioning the Patient for a 25o Isometric Lateral Test 25

Positioning the Patient for a 45 Degree Cervical

Isometric Strength Protocol 26

Positioning the Patient for a 45o Isometric Flexion/Extension Test 28

Positioning the Patient for a 45o Isometric Lateral Test 29

Utilizing the Cervical ROM Protocol 30

Accessing the Cervical Strength Protocols 30

Utilizing the Strength Flexion Test 31

Utilizing the Strength Extension Test 33

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Utilizing the Strength Lateral Test 34

Utilizing the Strength Protraction Test 36

Utilizing the Strength Retraction Test 37

Creating Custom Cervical Integration Protocols 38

Clinical Protocols 39

Utilizing Clinical Protocols 39

Editing and Creating Clinical Protocols 40

Super Protocols 41

Validity Analysis 43

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PROTOCOLS

Through the ODES software, you can access many pre-programmed protocols as well as cre-

ate customized protocols. The following protocol categories can be accessed through the Home

Screen:

•Self Reports •Cardio •ROM Tests •Strength Tests •Clinical Tests

BTE Technologies recommends that the MCU™ be used in conjunction with a certified training

program on The Melbourne Protocol. This training program covers the practical and clinical appli-

cation of Evaluation Protocols for patients suffering from various cervical disorders. Precautions,

indications, and contra-indications for the evaluation of patients on the MCU™ are also covered.

Refer to Section 10 for more information on this training program.

I. SELF REPORTS

ODES includes several pre-programmed Self Report protocols, which are intended to be com-

pleted without the use of any tools. These are typically questionnaires used to evaluate the

patient’s perceived level of injury and pain.

A. UTILIZING SELF REPORTS

Access the pre-programmed Self Reports protocols by clicking the Self Reports icon on the

Home Screen.

This will bring you to the Self Reports Protocols main page. From this page you have the

ability to access all the pre-programmed protocols, including those in hibernation, add and

remove tests to clients, create new range of motion tests, edit tests, and delete tests (Fig-

ure 6-1).

Step 1. Assign a test to a client by highlighting the test in the left box and clicking Add to

Client or by double clicking on the test in the left box.

Step 2. Once a test has been assigned to a client, highlight the test name in the right box

and click Perform Test to bring up the testing screen.

Step 3. Fill out the questionnaire using the following options: a) Read the questions aloud

and enter in the answers; b) Allow the patient to enter in the answers via the computer; c)

Print out the questionnaire and allow the patient to enter in the answers on the paper.

Step 4. Store and/or file the questionnaire according to your clinic’s procedures.

Figure 6-1. Self Reports Protocol Screen

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B. EDITING AND CREATING SELF REPORTS

Access the pre-programmed Self Reports protocols by clicking the Self Reports icon on the

Home Screen.

This will bring you to the Self Reports Protocols main page, where you can edit and create

tests.

Edit a test by highlighting the test you would like to edit in the left box and clicking Edit

Test.

Create a new test by clicking on New Test.

If you are editing a test, a screen will appear with the current settings of the test you

selected. If you are creating a test, a screen will appear with the same headings as if you

were editing a test, but all of the text fields will be blank (Figure 6-2).

Since editing and creating protocols are very similar, an example of an edited test will be

given, but the same guidelines apply for creating a test.The following can typically be ed-

ited or created on Custom Self Report Tests:

A. Test Name - Type in the name of the test

B. Section - Type in the sections to include in the test

C. Final Score Column Name - Type in the name of the final score column

D. Rating Column - Select whether to include a rating column and then type in the name of

the column

E. Examiner Description - Type in any description the examiner will need to perform the

test - this field is especially useful for supplying instructions on how to perform the evalu-

ation

F. Report Description - Type in any description that should be included on the report

G. Reference Information - Include any reference information that needs to be added to

the report

Once the screen has been closed, the protocol is saved under the assigned test name with

Figure 6-2. Custom Self Report

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the new specifications.

II. CARDIOVASCULAR PROTOCOLS

ODES includes several pre-programmed Cardiovascular protocols.

A. UTILIZING CARDIOVASCULAR PROTOCOLS

Access the pre-programmed Cardiovascular protocols by clicking the Cardio icon on the

Home Screen.

This will bring you to the Cardiovascular Protocols main page. From this page you have the

ability to access all the pre-programmed protocols, including those in hibernation, add and

remove tests to clients, create new range of motion tests, edit tests, and delete tests (Fig-

ure 6-3).

Step 1. Assign a test to a client by highlighting the test in the left box and clicking Add to

Client or by double clicking on the test in the left box.

Step 2. Once a test has been assigned to a client, highlight the test name in the right box

and click Perform Test to bring up the testing screen.

Step 3. Follow the instructions on the test screen.

B. EDITING AND CREATING CARDIOVASCULAR PROTOCOLS

Access the pre-programmed Cardiovascular protocols by clicking the Cardio icon on the

Home Screen.

This will bring you to the Cardiovascular Protocols main page, where you can edit and cre-

ate tests .

Edit a test by highlighting the test you would like to edit in the left box and clicking Edit

Test.

Create a new test by clicking on New Test.

If you are editing a test, a screen will appear with the current settings of the test you

selected. If you are creating a test, a screen will appear with the same headings as if you

were editing a test, but all of the text fields will be blank (Figure 6-4).

Figure 6-3. Cardiovascular Protocols

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Since editing and creating protocols are very similar, an example of an edited test will be

given, but the same guidelines apply for creating a test.

The following can typically be edited or created on Cardiovascular Tests:

A. Test Name - Type in the name of the test

B. Set Maximum Allowable Heart Rate - Select whether to set the maximum allowable

heart rate and at what percentage of age.

C. View Initial Heart Rate - Select whether to view the initial heart rate within the test

screen

D. View Peak Heart Rate - Select whether to view the peak heart rate within the test

screen

E. View Final Heart Rate - Select whether to view the final heart rate within the test

screen

F. View Percent Heart Rate Increase from Initial - Select whether to view the percent

heart rate increase from the initial within the test screen

G. View Recovery Heart Rate - Select whether to view the recovery heart rate within the

test screen and choose when to stop the recovery time

H. Use a Rating - Select whether to use a rating and then set the rating

I. Examiner Description - Type in any description the examiner will need to perform the

test - this field is especially useful for supplying instructions on how to perform the evalu-

ation

J. Report Description - Type in any description that should be included on the report

K. Reference Information - Include any reference information that needs to be added to

the report

L. Test Duration Options - Choose which method will determine test duration

M. Use a Metronome - Select whether to use a metronome and number of beats per minute

Figure 6-4. Custom Cardiovascular Protocol

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N. Parameters to be Measured (Heading Labels) - Type in the parameters that will be mea-

sured

Once the screen has been closed, the protocol is saved under the assigned test name with

the new specifications.

III. CERVICAL RANGE OF MOTION (ROM) PROTOCOLS

A. POSITIONING THE PATIENT FOR A CERVICAL ROM PROTOCOL

In order to prepare for cervical range of motion testing, it is extremely important to under-

stand how to properly position the patient; this will prevent any injury during testing.

The following 7 steps are required prior to each type of ROM testing. Outlined after these 7

initial steps are the subsequent steps, which vary according to the test being performed.

Step 1. Insert the range-of-motion stop pin in the zero degree position on the halo (Figure

6-5).

Step 2. Lower the chair all the way down to its lowest position.

Step 3. Using the latch on the right side, open the halo (Figure 6-6).

Step 4. Ask the patient to sit in the chair.

Step 5. Adjust the height of the seat, the position of the seat, the position of the back

of the chair, the height of the back of the chair, and the arm rests to accommodate the

patient’s size, height, and posture. Set the halo height to 3 as a starting position (Figure

6-7).

Figure 6-5. Insert

ROM Stop

Figure 6-6. Open Halo

Figure 6-7. Seat Adjustments

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Step 6. Secure the patient with the waist strap and shoulder straps (Figure 6-8).

Step 7. Close and lock the halo (Figure 6-9).

1. POSITIONING THE PATIENT FOR A ROM FLEXION OR EXTENSION TEST

Step 8. For a flexion test, insert both of the head braces in the halo. For an extension

test, insert the back head brace with a Velcro strap attached. Note that the bottom of

the back brace is located at the external occipital protuberance (Figure 6-10).

Step 9. Set the halo to 15 degrees below the horizontal (Figure 6-11).

Step 10. Position the head brace(s) against the patient’s head, but do not secure his/

her head in place.

Step 11. Make fine adjustments to the seat and halo such that C5/C6 of the patient’s

Figure 6-8. Waist and Shoulder Straps

Figure 6-9. Close

and Lock the Halo

Flexion Set-up Attaching Strap

for Extension

Location of

Back Brace

Figure 6-10. Initial ROM Flexion & Extension Set-ups

Figure 6-11. Halo Angle

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spine lines up with the pivot point of the halo (Figure 6-12).

Step 12. Firmly secure the patient’s head with the head brace(s) and Velcro strap (if

performing an extension test).

Step 13. Remove the range-of-motion stop pin before performing the test (Figure 6-13).

Note that the RJ45 cable is not required for this test.

2. POSITIONING THE PATIENT FOR A ROM L/R ROTATION TEST

Step 8. Insert both of the head braces in the halo (Figure 6-14).

Step 9. Set the halo to 0 degrees with respect to the horizontal and 10 degrees flexion

(Figure 6-15).

Step 10. Position the head braces against the patient’s head, but do not secure his/her

head in place.

Figure 6-12. Final Adjustments and Locating C5/C6

Flexion Extension

Figure 6-13. Final Set-ups for ROM Flexion & Extension

Figure 6-14. Insert

Both Head Braces

Figure 6-15. Set halo angles

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Step 11. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-16).

Step 12. Firmly secure the patient’s head with the head braces.

Step 13. While holding onto the side of the halo, unlock the rotation pin, which is locat-

ed at the top middle of the halo, before performing the test (Figure 6-17).

Note that the RJ45 cable is not required for this test.

3. POSITIONING THE PATIENT FOR A ROM LATERAL FLEXION TEST

Step 8. Unlock the rotation pin and rotate the halo to 90 degrees right rotation. Lock

the rotation pin back into place (Figure 6-18).

Step 9. Insert both of the head braces in the halo (Figure 6-19).

Step 10. Set the halo to 0 degrees with respect to the horizontal. Make sure the flexion/

extension angle is set to 0 degrees as well (Figure 6-20).

Figure 6-16. Final Adjustments and Locating C5/C6

Figure 6-17. Unlocking Rotation Pin and Final

ROM L/R Rotation Set-up

Unlock Rotation Pin Final Rotation Set-up

Figure 6-18. Halo at 90o Rotation

Figure 6-19. Attach Head Braces

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Step 11. Position the head braces against the patient’s head, but do not secure his/her

head in place.

Step 12. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-21).

Step 13. Firmly secure the patient’s head with the head braces.

Step 14. Remove the range-of-motion stop pin before performing the test (Figure 6-22).

Note that the RJ45 cable is not required for this test.

B. UTILIZING THE CERVICAL RANGE OF MOTION (ROM) PROTOCOL

1. ACCESSING THE CERVICAL ROM PROTOCOL

Access the pre-programmed ROM protocols by clicking the ROM Tests icon on the Home

Screen.

This will bring you to the ROM Protocols main page. From this page you have the abil-

ity to access all the pre-programmed protocols, including those in hibernation, add and

remove tests to clients, create new range of motion tests, edit tests, and delete tests.

Note that the Cervical Range of Motion protocol is the only pre-programmed ROM test

that will be needed for the MCU™ (Figure 6-23).

Figure 6-20. Set halo angles

Figure 6-21. Final Adjustments and Locating C5/C6

Figure 6-22. Final Set-up for ROM Lateral Flexion

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Step 1. Assign a test to a client by highlighting the test in the left box and clicking Add

to Client or by double clicking on the test in the left box.

Step 2. Once a test has been assigned to a client, highlight the test name in the right

box and click Perform Test to bring up the testing screen (Figure 6-24).

The initial Cervical Range of Motion protocol screen contains the following features:

• Name of the test

• Test number

• Start Test icon, which changes to Stop Test after the test has begun

• New icon to begin a new set of tests

• Delete icon to delete the selected test’s results

• Close icon to return to the protocol screen

• Next Protocol icon to move on to the next protocol

• Flexion icon, which switches to the Flexion test screen

• L/R Rotation icon, which switches to the Rotation test screen

Figure 6-23. Range of Motion Protocols

Figure 6-24. Cervical Range of Motion Main Screen

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• Lateral Flexion icon, which switches to the Lateral Flexion test screen

• Extension icon, which switches to the Extension test screen

• Graphs and tables to illustrate the test results

• Instructions on how to perform the tests

• Threshold icon, which allows a threshold force to be set

2. UTILIZING THE ROM FLEXION TEST

The ROM Flexion test measures the patient’s range of motion with respect to the flexor

muscle group.

Step 1. Select the Flexion icon. The Flexion Testing screen will appear (Figure 6-25).

Note that the screen shown in the figure may differ from that on the computer.

Step 2. Position the patient as described in Section 06-III of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The ROM Flexion test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average ROM, peak ROM,

coefficient of variation (COV), and the percent of normal. The pain rating determined by

the patient will also appear in the pain scale text field (Figure 6-26).

Figure 6-25. Cervical ROM - Flexion Test

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You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

3. UTILIZING THE ROM ROTATION TEST

The ROM Rotation test measures the patient’s range of motion with respect to the lat-

eral rotator muscle group.

Step 1. Select the L/R Rotation icon. The Rotation Testing screen will appear (Figure

6-27). Note that the screen shown in the figure may differ from that on the computer.

Figure 6-26. Cervical ROM - Completed Flexion Test

Figure 6-27. Cervical ROM - L/R Rotation Test

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Step 2. Position the patient as described in Section 06-III of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once each side is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The ROM Rotation test calls for three trials to be performed per side.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph. These figures are especially helpful in comparing

the abilities of each side.

In addition to the test results, the screen will tabulate: the average ROM, peak ROM, co-

efficient of variation (COV), the percent of normal, and the percent difference between

the left and right side. The pain ratings determined by the patient will also appear in

the pain scale text fields (Figure 6-28).

You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

4. UTILIZING THE ROM LATERAL FLEXION TEST

The ROM Lateral Flexion test measures the patient’s range of motion with respect to the

lateral flexor muscle group.

Step 1. Select the Lateral Flexion icon. The Lateral Flexion Testing screen will appear

(Figure 6-29). Note that the screen shown in the figure may differ from that on the com-

puter.

Figure 6-28. Cervical ROM - Completed L/R Rotation Test

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Step 2. Position the patient as described in Section 06-III of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once each side is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The ROM Lateral Flexion test calls for three trials to be performed per side.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph. These figures are especially helpful in comparing

the abilities of each side.

In addition to the test results, the screen will tabulate: the average ROM, peak ROM, co-

efficient of variation (COV), the percent of normal, and the percent difference between

the left and right side. The pain ratings determined by the patient will also appear in

the pain scale text fields (Figure 6-30).

Figure 6-29. Cervical ROM - Lateral Flexion Test

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You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

5. UTILIZING THE ROM EXTENSION TEST

The ROM Extension protocol measures the patient’s range of motion with respect to the

extensor muscle group.

Step 1. Select the Extension icon. The Extension Testing screen will appear (Figure 6-

31). Note that the screen shown in the figure may differ from that on the computer.

Figure 6-30. Cervical ROM - Completed Lateral Flexion Test

Figure 6-31. Cervical ROM - Extension Test

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Step 2. Position the patient as described in Section 06-III of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient determined and then click OK.

The ROM Extension test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average ROM, peak ROM,

coefficient of variation (COV), and the percent of normal. The pain rating determined by

the patient will also appear in the pain scale text field (Figure 6-32).

You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

IV. STRENGTH PROTOCOLS

A. POSITIONING THE PATIENT FOR NEUTRAL CERVICAL ISOMETRIC STRENGTH PRO-

TOCOLS

In order to prepare for cervical strength testing, it is extremely important to understand

how to properly position the patient; this will prevent any injury during testing.

The following 7 steps are required prior to each type of strength testing. Outlined after

these 7 initial steps are the subsequent steps, which vary according to the test being per-

formed.

Step 1. Insert the range-of-motion stop pin in the zero degree position on the halo (Figure

6-33).

Figure 6-32. Cervical ROM - Completed Extension Test

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Step 2. Lower the chair all the way down to its lowest position.

Step 3. Using the latch on the right side, open the halo (Figure 6-34).

Step 4. Ask the patient to sit in the chair.

Step 5. Adjust the height of the seat, the position of the seat, the position of the back

of the chair, the height of the back of the chair, and the arm rests to accommodate the

patient’s size, height, and posture. Set the halo height to 3 as a starting position (Figure

6-35).

Step 6. Secure the patient with the waist strap and shoulder straps (Figure 6-36).

Step 7. Close and lock the halo (Figure 6-37).

Figure 6-36. Waist and Shoulder Straps

Figure 6-33 Insert

ROM Stop

Figure 6-34. Open Halo

Figure 6-35. Seat Adjustments

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1. POSITIONING THE PATIENT FOR AN ISOMETRIC FLEXION/EXTENSION TEST

Step 8. For a flexion test, insert the front head brace. For an extension test, insert the

back head brace. Note that the bottom of the back brace is located at the external oc-

cipital protuberance (Figure 6-38).

Step 9. Set the halo to 15 degrees below the horizontal (Figure 6-39).

Step 10. Position the head brace against the patient’s head.

Step 11. Make fine adjustments to the seat and halo such that C5/C6 of the patient’s

spine lines up with the pivot point of the halo (Figure 6-40).

Step 12. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

Figure 6-37. Close

and Lock the Halo

Figure 6-39. Halo Angle

Figure 6-40. Final Adjustments and Locating C5/C6

Location of

Back Brace

Figure 6-38. Initial Isometric Flexion

& Extension Set-up

Flexion Set-up

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closest to the front of the unit at the top of the MCU™ (Figure 6-41).

2. POSITIONING THE PATIENT FOR A ISOMETRIC LATERAL TEST

Step 8. Unlock the rotation pin and rotate the halo to 90 degrees right rotation. Lock

the rotation pin (Figure 6-42).

Step 9. Attach the head brace to the halo on the side being tested (Figure 6-43).

Step 10.

Set the halo to 0 degrees with respect to the horizontal. Make sure the flexion/

extension angle is set to 0 degrees as well (Figure 6-44).

Step 11. Position the head brace against the patient’s head.

Step 12. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-45).

Flexion Extension

Figure 6-41. MCU™ RJ45 Jack and Final Isometric Flexion & Extension Set-ups

Figure 6-42. Halo at 90o Rotation

Figure 6-43. Attach Head Brace

Figure 6-44. Set halo angles

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Step 13. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

closest to the front of the unit at the top of the MCU™ (Figure 6-46).

B. POSITIONING THE PATIENT FOR 25 DEGREE CERVICAL ISOMETRIC STRENGTH

PROTOCOLS

In order to prepare for cervical strength testing, it is extremely important to understand

how to properly position the patient; this will prevent any injury during testing.

The following 7 steps are required prior to each type of strength testing. Outlined after

these 7 initial steps are the subsequent steps, which vary according to the test being per-

formed.

Step 1. Insert the range-of-motion stop pin in the zero degree position on the halo (Figure

6-47).

Step 2. Lower the chair all the way down to its lowest position.

Step 3. Using the latch on the right side, open the halo (Figure 6-48).

Figure 6-45. Final Adjustments and Locating C5/C6

Figure 6-46. MCU™ RJ45 Jack and Final Isometric Lateral Set-up

Figure 6-47. Insert

ROM Stop

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Step 4. Ask the patient to sit in the chair.

Step 5. Adjust the height of the seat, the position of the seat, the position of the back

of the chair, the height of the back of the chair, and the arm rests to accommodate the

patient’s size, height, and posture (Figure 6-49).

Step 6. Secure the patient with the waist strap and shoulder straps (Figure 6-50).

Step 7. Close and lock the halo (Figure 6-51).

Figure 6-50. Waist and Shoulder Straps

Figure 6-48. Open Halo

Figure 6-51. Close

and Lock the Halo

Figure 6-49. Seat Adjustments

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1. POSITIONING THE PATIENT FOR A 25 DEGREE ISOMETRIC FLEXION/EXTENSION TEST

Step 8. For a flexion test, insert the front head brace. For an extension test, insert the

back head brace. Note that the bottom of the back brace is located at the external oc-

cipital protuberance (Figure 6-52).

Step 9. Set the halo to 15 degrees below the horizontal (Figure 6-53).

Step 10. Position the head brace against the patient’s head.

Step 11. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-54).

Step 12. While holding onto the side of the halo, unlock the rotation pin, which is lo-

cated at the top middle of the halo. If you’re testing the patient’s left side, rotate the

halo 25 degrees right and then lock the rotation pin. Rotate the halo 25 degrees to the

left to test the patient’s right side (Figure 6-55).

Figure 6-54. Final Adjustments and Locating C5

Figure 6-53. Halo Angle

Location of

Back Brace

Figure 6-52. Initial Isometric Flexion

& Extension Set-up

Flexion Set-up

Unlock Rotation Pin 25o Right

Figure 6-55. Halo Rotation of 25o

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Step 13. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

closest to the front of the unit at the top of the MCU™ (Figure 6-56).

2. POSITIONING THE PATIENT FOR A 25 DEGREE ISOMETRIC LATERAL TEST

Step 8. Unlock the rotation pin, which is located at the top middle of the halo. If

you’re testing the patient’s left side, rotate the halo 65 degrees toward the right, and

then lock the rotation pin. Rotate the halo 65 degrees toward the left when testing the

patient’s right side (Figure 6-57). Note that the figures show a set-up for testing the

patient’s right side.

Step 9. Attach the head brace to the halo on the side being tested (Figure 6-58).

Step 10. Set the halo to 0 degrees with respect to the horizontal. Make sure the flexion/

extension angle is set to 0 degrees as well (Figure 6-59).

Step 11. Position the head brace against the patient’s head.

Step 12. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

Flexion Extension

Figure 6-56. MCU™ RJ45 Jack and Final 25o Isometric Flexion & Extension Set-ups

Figure 6-57. Halo Rotation of 25o Lateral

Figure 6-58. Attach Head Brace

Figure 6-59. Set halo angles

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the pivot point of the halo (Figure 6-60).

Step 13. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

closest to the front of the unit at the top of the MCU™ (Figure 6-61).

C. POSITIONING THE PATIENT FOR 45 DEGREE CERVICAL ISOMETRIC STRENGTH

PROTOCOLS

In order to prepare for cervical strength testing, it is extremely important to understand

how to properly position the patient; this will prevent any injury during testing.

The following 7 steps are required prior to each type of strength testing. Outlined after

these 7 initial steps are the subsequent steps, which vary according to the test being per-

formed.

Step 1. Insert the range-of-motion stop pin in the zero degree position on the halo (Figure

6-62).

Step 2. Lower the chair all the way down to its lowest position.

Step 3. Using the latch on the right side, open the halo (Figure 6-63).

Figure 6-61. MCU™ RJ45 Jack and Final

25o Isometric Lateral Set-up

Figure 6-60. Final Adjustments and Locating C5

Figure 6-62. Insert

ROM Stop

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Step 4. Ask the patient to sit in the chair.

Step 5. Adjust the height of the seat, the position of the seat, the position of the back

of the chair, the height of the back of the chair, and the arm rests to accommodate the

patient’s size, height, and posture. Set the halo height to 3 as a starting position (Figure

6-64).

Step 6. Secure the patient with the waist strap and shoulder straps (Figure 6-65).

Step 7. Close and lock the halo (Figure 6-66).

Figure 6-65. Waist and Shoulder Straps

Figure 6-63. Open Halo

Figure 6-66. Close

and Lock the Halo

Figure 6-64. Seat Adjustments

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1. POSITIONING THE PATIENT FOR A 45 DEGREE ISOMETRIC FLEXION/EXTENSION TEST

Step 8. For a flexion test, insert the front head brace. For an extension test, insert the

back head brace. Note that the bottom of the back brace is located at the external oc-

cipital protuberance (Figure 6-67).

Step 9. Set the halo to 15 degrees below the horizontal (Figure 6-68).

Step 10. Position the head brace against the patient’s head.

Step 11. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-69).

Step 12. While holding onto the side of the halo, unlock the rotation pin, which is lo-

cated at the top middle of the halo. If you’re testing the patient’s left side, rotate the

halo to 45 degrees right rotation and then lock the rotation pin. Rotate the halo to 45

degrees left rotation to test the patient’s right side (Figure 6-70).

Figure 6-69. Final Adjustments and Locating C5/C6

Figure 6-68. Halo Angle

Location of

Back Brace

Figure 6-67. Initial Isometric Flexion

& Extension Set-up

Flexion Set-up

Unlock Rotation Pin

Figure 6-70. Halo Rotation of 45o

45o Right

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Step 13. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

closest to the front of the unit at the top of the MCU™ (Figure 6-71).

2. POSITIONING THE PATIENT FOR A 45 DEGREE ISOMETRIC LATERAL TEST

Step 8. Unlock the rotation pin, which is located at the top middle of the halo. If

you’re testing the patient’s left side, rotate the halo to 45 degrees right rotation, and

then lock the rotation pin. Rotate the halo to 45 degrees left rotation when testing the

patient’s right side (Figure 6-72). Note that the figures show a set-up for testing the

patient’s right side.

Step 9. Attach the head brace to the halo on the side being tested (Figure 6-73).

Step 10. Set the halo to 0 degrees with respect to the horizontal. Make sure the flexion/

extension angle is set to 0 degrees as well (Figure 6-74).

Step 11. Position the head brace against the patient’s head.

Step 12. Make fine adjustments to the seat to line up C5/C6 of the patient’s spine with

the pivot point of the halo (Figure 6-75).

Flexion Extension

Figure 6-71. MCU RJ45 Jack and Final 25o Isometric Flexion & Extension Set-ups

Figure 6-73. Attach Head Brace

Figure 6-74. Set halo angles

Figure 6-72. Halo Rotation of 45o Lateral

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Step 13. Attach the RJ45 cable to the head brace being used and the RJ45 jack that is

closest to the front of the unit at the top of the MCU™ (Figure 6-76).

D. UTILIZING THE CERVICAL STRENGTH PROTOCOLS

1. ACCESSING THE CERVICAL STRENGTH PROTOCOLS

Access the pre-programmed Strength protocols by clicking the Strength Tests icon on

the Home Screen.

This will bring you to the Strength Protocols main page. From this page you have the

ability to access all the pre-programmed protocols, including those in hibernation, add

and remove tests to clients, create new isometric strength tests, edit tests, and delete

tests (Figure 6-77).

Note that three strength protocols have been designed for the Multi-Cervical™ Unit:

MCU™ Neutral Isometric, MCU™ Angle Specific 25 Degrees, and MCU™ Angle Specific 45

Degrees. The only difference between the three protocols is the rotation angle at which

Figure 6-75. Final Adjustments and Locating C5/C6

Figure 6-76. MCU™ RJ45 Jack and Final

45o Isometric Lateral Set-up

Figure 6-77. Strength Protocols

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the halo is set (i.e. 0 degrees, 25 degrees, and 45 degrees).

Step 1. Assign a test to a client by highlighting the test in the left box and clicking Add

to Client or by double clicking on the test in the left box.

Step 2. Once a test has been assigned to a client, highlight the test name in the right

box and click Perform Test to bring up the testing screen (Figure 6-78).

The initial Cervical Strength protocol screens contain the following features:

• Name of the test

• Start Test icon, which changes to Stop Test after the test has begun

• Analysis icon to extensively analyze the data of a completed test

• New icon to begin a new set of test results

• Delete icon to delete the selected test’s results

• Close icon to return to the protocol screen

• Next Protocol icon to move on to the next protocol

• Flexion icon, which switches to the Flexion test screen

• Extension icon, which switches to the Extension test screen

• Lateral icon, which switches to the Lateral test screen

• Protraction icon, which switches to the Protraction screen

• Retraction icon, which switches to the Retraction screen

• Graphs and tables to illustrate the test results

• Instructions on how to perform the tests

• Threshold icon, which allows a threshold force to be set

2. UTILIZING THE STRENGTH FLEXION TEST

The Strength Flexion test measures the patient’s strength with respect to the flexor

muscle group.

Step 1. Select the Flexion icon. The Flexion Testing screen will appear (Figure 6-79).

Note that the screen shown in the figure may differ from that on the computer.

Figure 6-78. Cervical Strength Main Screen

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Step 2. Position the patient as described in Section 06-IV of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The Strength Flexion test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average force, peak force,

coefficient of variation (COV), and the percent of normal. The pain ratings determined

by the patient will also appear in the pain scale text field (Figure 6-80).

Figure 6-79. Cervical Strength - Flexion Test

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You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

3. UTILIZING THE STRENGTH EXTENSION TEST

The Strength Extension test measures the patient’s strength with respect to the exten-

sor muscle group.

Step 1. Select the Extension icon. The Extension Testing screen will appear (Figure 6-

81). Note that the screen shown in the figure may differ from that on the computer.

Figure 6-80. Cervical Strength - Completed Flexion Test

Figure 6-81. Cervical Strength - Extension Test

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Step 2. Position the patient as described in Section 06-IV of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The Strength Extension test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average force, peak force,

coefficient of variation (COV), and the percent of normal. The pain ratings determined

by the patient will also appear in the pain scale text field (Figure 6-82).

You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

4. UTILIZING THE STRENGTH LATERAL TEST

The Strength Lateral test measures the patient’s strength with respect to the lateral

muscle group.

Step 1. Select the Lateral icon. The Lateral Testing screen will appear (Figure 6-83).

Note that the screen shown in the figure may differ from that on the computer.

Figure 6-82. Cervical Strength - Completed Extension Test

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Step 2. Position the patient as described in Section 06-IV of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once each side is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient determined and then click OK.

The Strength Lateral test calls for three trials to be performed per side.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average force, peak force,

coefficient of variation (COV), and the percent of normal. The pain ratings determined

by the patient will also appear in the pain scale text field (Figure 6-84).

Figure 6-83. Cervical Strength - Lateral Test

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You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

5. UTILIZING THE STRENGTH PROTRACTION TEST

Step 1. Select the Protraction icon. The Protraction Testing screen will appear (Figure

6-85). Note that the screen shown in the figure may differ from that on the computer.

Step 2. Position the patient as described in Section 06-IV of this manual.

Figure 6-84. Cervical Strength - Completed Lateral Test

Figure 6-85. Cervical Strength - Protraction Test

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Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The Strength Protraction test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average force, peak force,

coefficient of variation (COV), and the percent of normal. The pain ratings determined

by the patient will also appear in the pain scale text field.

You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

6. UTILIZING THE STRENGTH RETRACTION TEST

Step 1. Select the Retraction icon. The Retraction Testing screen will appear (Figure

6-86). Note that the screen shown in the figure may differ from that on the computer.

Step 2. Position the patient as described in Section 06-IV of this manual.

Step 3. Click Start Test to begin testing.

Step 4. Once the test is completed, a pain scale will appear. Ask the patient to rate

his/her pain on a ten-point scale (0 is equivalent to no pain and 10 is equivalent to the

worst pain possible). Click on the number the patient stated and then click OK.

The Retraction Strength test calls for three trials to be performed.

As the protocol is performed, the screen will display the results and averages via a line

graph, table, pie chart, and bar graph.

In addition to the test results, the screen will tabulate: the average force, peak force,

Figure 6-86. Cervical Strength - Retraction Test

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coefficient of variation (COV), and the percent of normal. The pain ratings determined

by the patient will also appear in the pain scale text field.

You may retest a trial by clicking on the R icon to the left or right of the trial table, de-

pending on which trial you would like to redo. However, once a test has been closed, the

trials can not be retested.

7. CREATING CUSTOM CERVICAL INTEGRATION PROTOCOLS

Access the pre-programmed Strength protocols by clicking the Strength Tests icon on

the Home Screen.

This will bring you to the Strength Protocols main page, where you can edit and create

tests.

Create a new test by clicking on New Test and then clicking Cervical Integration (Fig-

ure 6-87).

The following can be created on Custom Cervical Integration Protocols:

A. Cervical Protocol Name - Type in the name of the test

B. Maximum Trial Duration - Set the maximum amount of time (seconds) for the trial

duration

C. Rest Period Between Trials - Set the amount of time (seconds) to rest between trials

D. Rest Period Between Sides - Set the amount of time (seconds) to rest between

switching sides

E. Fixed Initial Rotation Angle (deg) - Set the initial angle (degrees) for a rotation test

F. Test Description - Type in any description that should be included on the test

G. Insert Password - Choose whether a password is required to edit the test – if this op-

tion is selected, any user will be prompted for the password whenever he or she tries to

edit the test.

H. Body Region - Select which body region is to be evaluated

I. Fixed Initial Flexion/Extension Angle (deg) - Set the initial (degrees) for a flexion or

extension test

J. Flexion/Extension Threshold (lbs) - Set the amount of force (lbs) required for a flex-

Figure 6-87. Custom Cervical Integration Protocol

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ion or extension test to begin

K. Rotation Threshold (lbs) - Set the amount of force (lbs) required for a rotation test to

begin

L. Pain Rating Per Side - Choose whether to display the pain rating scale

Once the screen has been closed, the protocol is saved under the assigned test name

with the new specifications.

V. CLINICAL PROTOCOLS

ODES includes several pre-programmed Clinical protocols, which are intended to be completed

without the use of any tools. These protocols help to identify any injuries or anomalies the pa-

tient may have.

A. UTILIZING CLINICAL PROTOCOLS

Access the pre-programmed Clinical protocols by clicking the Clinical icon on the Home

Screen.

This will bring you to the Clinical Protocols main page. From this page you have the ability

to access all the pre-programmed protocols, including those in hibernation, add and re-

move tests to clients, create new range of motion tests, edit tests, and delete tests (Figure

6-88).

Step 1. Assign a test to a client by highlighting the test in the left box and clicking Add to

Client or by double clicking on the test in the left box.

Step 2. Once a test has been assigned to a client, highlight the test name in the right box

and click Perform Test to bring up the testing screen (Figure 6-89).

Figure 6-88. Clinical Protocols

BTE Technologies WER-1 MCU Wireless User Manual 40040005 rev 000

BTE Technologies, Inc. MCU Wireless 40040005 rev 000

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