Effectiveness of a Wheelchair Skills Training Program for Power Mobility Users: A Randomized Controlled Trial

Sponsor
Nova Scotia Health Authority (Other)
Overall Status
Completed
CT.gov ID
NCT01432418
Collaborator
Canadian Institutes of Health Research (CIHR) (Other)
116
6
2
27
19.3
0.7

Study Details

Study Description

Brief Summary

This is a 3-year multi-centre, single-blinded, randomized controlled trial (RCT) to test the hypothesis that wheelchair skills training (using a systematic training program called the Wheelchair Skills Training Program) improves wheelchair skills and safety of 144 powered wheelchair users. A second objective is to assess the effects of age, sex, training centre, and participant experience on outcomes, assessing the retention of benefits and assessing the impact of training on other important outcomes.

Condition or Disease Intervention/Treatment Phase
  • Other: Wheelchair skills training program
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Effectiveness of a Wheelchair Skills Training Program for Power Mobility Users: A Randomized Controlled Trial
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Sep 1, 2014
Actual Study Completion Date :
Sep 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: wheelchair training

Other: Wheelchair skills training program
A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.

No Intervention: Control

Standard of care only

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in Wheelchair Skills, WST 4.1 questionnaire version [baseline, 1 month , 3 months]

    A measure of what the person 'can do' (capacity), 'does do' (performance), and the safety of various wheelchair skills. The Wheelchair Skills Test (WST) version 4.1 in questionnaire format will be used.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • new or experienced powered wheelchair users

  • use or are expected to use powered wheelchairs for at least 4 hrs/week

  • have access to a powered wheelchair with a suitable range of controller settings (i.e. able to climb a 5cm level change) for testing and training

  • equal or greater than 18 years of age

  • able to follow directions in either French or English (whichever is in use at the participating site)

  • have the potential to operate their powered wheelchairs independently

  • have room for improvement (in the opinion of the potential participant's clinician)

  • requires no more than minimal assistance for communication and auditory comprehension (in the opinion of the potential participant's clinician)

  • able to follow 2-step commands

  • demonstrate the ability to attend training sessions during the intake session

  • competent to provide their own informed consent

  • able to be comfortably seated in the powered wheelchairs that will be used for the study (if not their own).

Exclusion Criteria:
  • use or are expected to use a scooter

  • have a rapidly progressive disorder (e.g. amyotrophic lateral sclerosis or terminal cancer)

  • have significant visual impairments (legally blind)

  • have unstable medical conditions (e.g. angina, seizures)

  • have emotional problems (e.g. severe anxiety, depression) that might make participation unsafe or unpleasant

Contacts and Locations

Locations

Site City State Country Postal Code
1 GFS Rehabilitation Centre Vancouver British Columbia Canada V5Z 2G9
2 Nova Scotia Rehabilitation Centre Halifax Nova Scotia Canada B3H 4K4
3 University of Western Ontario London Ontario Canada N6G 1H1
4 Toronto Rehab Toronto Ontario Canada M5G 1V7
5 Centre de Réadaptation Lucie-Bruneau Montreal Quebec Canada H2H 2N8
6 Centre Interdisciplinaire de Recherche en Réadaptation et Intégration Sociale Quebec City Quebec Canada G1M 2S8

Sponsors and Collaborators

  • Nova Scotia Health Authority
  • Canadian Institutes of Health Research (CIHR)

Investigators

  • Principal Investigator: Lee Kirby, MD, FRCP, Nova Scotia Health Authority

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Lee Kirby, Attending Staff Physician, Department of Medicine, Nova Scotia Health Authority
ClinicalTrials.gov Identifier:
NCT01432418
Other Study ID Numbers:
  • 230378
  • CDHA-RS/2012-133
First Posted:
Sep 13, 2011
Last Update Posted:
May 9, 2016
Last Verified:
May 1, 2016
Keywords provided by Lee Kirby, Attending Staff Physician, Department of Medicine, Nova Scotia Health Authority
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 9, 2016