Skip to main content
Clinical Trials/NCT00392860
NCT00392860
Completed
Phase 2

Development of an Ergonomic Manual Wheelchair Pushrim- Phase II

VA Pittsburgh Healthcare System1 site in 1 country4 target enrollmentAugust 2008

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Spinal Cord Injury
Sponsor
VA Pittsburgh Healthcare System
Enrollment
4
Locations
1
Primary Endpoint
Change in Functional Status Score
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to test the effectiveness of newly designed ergonomic manual wheelchair handrims called the Natural-Fit and PalmRim when compared to a new standard handrim. It is our hope that the new design of the handrims will help reduce upper extremity pain and injury, which is very common among manual wheelchair users. The Natural-Fit handrim was designed to directly address the shortcomings of standard handrims and to improve the standard-round tube handrims which were designed over 50 years ago. The PalmRim was designed for individuals who have limited hand function, making it difficult to grasp standard handrims.

Detailed Description

This research will have three parts. The first part will include completing propulsion and braking tasks with the subject's original handrims. After the initial testing, new handrims (NaturalFit, PalmRim, and a new standard handrim) will be installed on the subject's wheelchair and subjects will again be asked to complete another set of propulsion and braking tasks. Subjects will also be asked to complete a questionnaire to assess wrist and shoulder pain and undergo an examination of the condition of the palm of their hand. For the second part of the study, subjects will be asked to participate in a 4-month trial use period of the new handrims on their wheelchair. In the third part of the study, subjects will complete the final set of propulsion and braking tasks and complete a follow-up questionnaire.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
September 2011
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michael Boninger

Chair, Department of Physical Medicine and Rehabilitation

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Use of a manual wheelchair as a primary means of mobility (over 40 hours per week)
  • Use a standard handrim
  • Between the ages of 18 and 55
  • Has normal hand function

Exclusion Criteria

  • Pressure Sores
  • Inclusion Criteria:
  • Use of a manual wheelchair as a primary means of mobility (over 40 hours per week)
  • Use a vinyl-coated handrim
  • Between ages 18 and 55
  • Has impaired hand function
  • Exclusion Criteria:
  • Pressure sores

Outcomes

Primary Outcomes

Change in Functional Status Score

Time Frame: Baseline, 4 Months

The Functional Status Scale, which measures hand and wrist symptoms.

Study Sites (1)

Loading locations...

Similar Trials