Effectiveness of a Wheelchair Skills Training Program for Power Mobility Users: A Randomized Controlled Trial
2 other identifiers
interventional
116
1 country
6
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2012
Typical duration for not_applicable
6 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 8, 2011
CompletedFirst Posted
Study publicly available on registry
September 13, 2011
CompletedStudy Start
First participant enrolled
June 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2014
CompletedMay 9, 2016
May 1, 2016
2.3 years
September 8, 2011
May 6, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in Wheelchair Skills, WST 4.1 questionnaire version
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.
baseline, 1 month , 3 months
Study Arms (2)
wheelchair training
EXPERIMENTALControl
NO INTERVENTIONStandard of care only
Interventions
A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.
Eligibility Criteria
You may qualify if:
- 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).
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (6)
GFS Rehabilitation Centre
Vancouver, British Columbia, V5Z 2G9, Canada
Nova Scotia Rehabilitation Centre
Halifax, Nova Scotia, B3H 4K4, Canada
University of Western Ontario
London, Ontario, N6G 1H1, Canada
Toronto Rehab
Toronto, Ontario, M5G 1V7, Canada
Centre de Réadaptation Lucie-Bruneau
Montreal, Quebec, H2H 2N8, Canada
Centre Interdisciplinaire de Recherche en Réadaptation et Intégration Sociale
Québec, Quebec, G1M 2S8, Canada
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lee Kirby, MD, FRCP
Nova Scotia Health Authority
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Attending Staff Physician, Department of Medicine
Study Record Dates
First Submitted
September 8, 2011
First Posted
September 13, 2011
Study Start
June 1, 2012
Primary Completion
September 1, 2014
Study Completion
September 1, 2014
Last Updated
May 9, 2016
Record last verified: 2016-05