Manual Wheelchair Propulsion Training

Not Applicable

Completed

• Conditions: Manual Wheelchair Users
• Interventions: Procedure: Instruction Only; Procedure: Instruction and Feedback

• Registration Number: NCT00226252
• Lead Sponsor: VA Pittsburgh Healthcare System

Brief Summary

The purpose of this research study is to investigate a manual wheelchair training program to improve the way manual wheelchair users push their wheelchairs.

Detailed Description

The purpose of this research is to create a manual wheelchair propulsion-training program (MWPTP) that emphasizes propulsion techniques that improve the manual wheelchair users stroke pattern and efficiency. It is our hope that the design of a manual wheelchair-training program can help to minimize the upper extremity pain and injury often associated with manual wheelchair propulsion.

The MWPTP will exist in three forms, and will be given to three randomly assigned groups of subjects. An instruction only group (IO) will receive general instructions on how to best propel their wheelchair. A feedback group (FB) will receive additional instruction in wheelchair propulsion using a monitor displaying a random combination and amount of biomechanical feedback variables, such as cadence and proportion of time spent in propulsion. Subjects will be coached to develop an appropriate propulsion style that minimizes all of the predetermined feedback measures, which indicate poor technique and maximize all of the graphical measures indicating good propulsion technique. A control group (CG) will receive only testing which will be identical to the testing procedures followed by the IO and FB groups.

Participation in this study will consist of four visits to the Human Engineering Research Lab (HERL) for the FB, IO and CG. Visits 1-4 will be the same, except visit 4 will not include training for any of the groups. All subjects will use their own wheelchair and cushion; however researchers will attach SMART Wheels TM to the subjects' wheelchair in place of their current wheels. The SMART Wheels TM are used to record the forces and moments that occur during propulsion and will not alter the dimensions or feel of the subjects current wheelchair. During each visit, all subjects will be asked to push over a real life course that includes various grades and surfaces. Then they will be asked to push on a wheelchair dynamometer at 1 meter/sec for one minute, 2 meter/sec for one minute, and a self selected speed for one minute. During this time, data will may also be collected with use of an Optotrak kinematic measurement system that incorporates a camera 3D-motion analysis system.

Study Timeline

• Study Start: 2003-12
• Study First Submitted: 2005-09-22
• Study First Submitted QC: 2005-09-22
• Study First Posted: 2005-09-26
• Primary Completion: 2008-03
• Study Completion: 2012-11
• Status Verified: 2013-03
• Last Update Submitted: 2013-03-11
• Last Update Posted: 2013-03-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

• 18 years of age or greater
• Use of a manual wheelchair as primary means of mobility (>80% of their ambulation)
• Spinal Cord Injury (SCI) cervical 7 level and lower

Exclusion Criteria

• Wheelchair athletes having competed in racing in the last year.
• Current upper limb pain that limits mobility.
• <1 year post inpatient rehabilitation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Instruction Only (IO)	Instruction Only	IO participants will train on the dynamometer for the same length of time as the Feedback Group. They will only be instructed to follow what they learned from the video presented at the beginning of the training session.
Instruction and Feedback Group (FB)	Instruction and Feedback	The FB group will receive video training, and real time feedback from the SMART Wheel as they push their wheelchair. A monitor displaying a random combination and amount of biomechanical feedback variables will be placed in front of subjects. Subjects will be instructed to adjust their stroke to optimize their biomechanics with feedback from the screen.

Primary Outcome Measures

Name	Time	Method
Stroke frequency, peak forces, time spent in propulsion	initial visit, visit 2 (1 week later), visit 3 (2 weeks later), visit 4 (3 months from initial visit)
Stroke pattern	initial visit, visit 2 (1 week later), visit 3 (2 weeks later), and visit 4 (3 months from initial visit).

Trial Locations

Locations (1)

Human Engineering Research Laboratories; 🇺🇸 Pittsburgh, Pennsylvania, United States