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Manual Wheelchair Propulsion Training

Manual Wheelchair Propulsion Training

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00226252
Enrollment
28
Registered
2005-09-26
Start date
2003-12-31
Completion date
2012-11-30
Last updated
2013-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Manual Wheelchair Users

Keywords

Wheelchair, Propulsion, Biomechanics

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.

Interventions

PROCEDUREInstruction Only

Video details an individual propelling a manual wheelchair with biomechanically correct propulsion technique.

PROCEDUREInstruction and Feedback

Individuals will watch video of correct propulsion technique and will receive real-time feedback from the SMART Wheel as they push their wheelchair to help optimize their propulsion technique.

Sponsors

University of Pittsburgh
CollaboratorOTHER
VA Pittsburgh Healthcare System
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Stroke frequency, peak forces, time spent in propulsioninitial visit, visit 2 (1 week later), visit 3 (2 weeks later), visit 4 (3 months from initial visit)
Stroke patterninitial visit, visit 2 (1 week later), visit 3 (2 weeks later), and visit 4 (3 months from initial visit).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026