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Manual Wheelchair Propulsion Training
This study is not yet open for participant recruitment.
Verified by VA Pittsburgh Healthcare System, September 2005
Sponsored by: VA Pittsburgh Healthcare System
Information provided by: VA Pittsburgh Healthcare System
ClinicalTrials.gov Identifier: NCT00226252
  Purpose

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


Condition Intervention
Manual Wheelchair Users
Procedure: Manual wheelchair skills training program

U.S. FDA Resources
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Manual Wheelchair Propulsion Training

Further study details as provided by VA Pittsburgh Healthcare System:

Primary Outcome Measures:
  • Stroke frequency, peak forces, time spent in propulsion at initial visit, visit 2 (1 week later), visit 3 (2 weeks later), and visit 3 (3 months from initial visit).
  • Stroke pattern utilized at initial visit, visit 2 (1 week later), visit 3 (2 weeks later), and visit 3 (3 months from initial visit).

Estimated Enrollment: 40
Study Start Date: January 2006
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 assign 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 stroke pattern, cadence, peak forces, proportion of time spent in propulsion (PSP) and rate of rise of force. A control group (CG) will receive only testing which will be identical to the testing procedures followed by the IO and FB groups. 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.

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 also be collected with use of an Optotrak kinematic measurement system that incorporates a camera 3D-motion analysis system.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00226252

Contacts
Contact: Ian Rice, MS, OT 412-365-4850 imr1@pitt.edu
Contact: Annmarie R Kelleher, MS, OTR/L 412-365-4850 kelleherar@herlpitt.org

Locations
United States, Pennsylvania
Human Engineering Research Laboratories
Pittsburgh, Pennsylvania, United States, 15206
Sponsors and Collaborators
VA Pittsburgh Healthcare System
Investigators
Principal Investigator: Michael L Boninger, MD University of Pittsburgh and VA Pittsburgh Healthcare System
  More Information

Human Engineering Research Laboratories  This link exits the ClinicalTrials.gov site

Study ID Numbers: 02159
Study First Received: September 22, 2005
Last Updated: November 15, 2005
ClinicalTrials.gov Identifier: NCT00226252  
Health Authority: United States: Federal Government

Keywords provided by VA Pittsburgh Healthcare System:
Wheelchair
Propulsion
Biomechanics

ClinicalTrials.gov processed this record on January 16, 2009