Effectiveness of a Wheelchair Skills Training Program for Power Mobility Users: A Randomized Controlled Trial
NCT ID: NCT01432418
Last Updated: 2016-05-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
116 participants
INTERVENTIONAL
2012-06-30
2014-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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wheelchair training
Wheelchair skills training program
A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.
Control
Standard of care only
No interventions assigned to this group
Interventions
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Wheelchair skills training program
A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
Nova Scotia Health Authority
OTHER
Responsible Party
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Lee Kirby
Attending Staff Physician, Department of Medicine
Principal Investigators
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Lee Kirby, MD, FRCP
Role: PRINCIPAL_INVESTIGATOR
Nova Scotia Health Authority
Locations
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GFS Rehabilitation Centre
Vancouver, British Columbia, Canada
Nova Scotia Rehabilitation Centre
Halifax, Nova Scotia, Canada
University of Western Ontario
London, Ontario, Canada
Toronto Rehab
Toronto, Ontario, Canada
Centre de Réadaptation Lucie-Bruneau
Montreal, Quebec, Canada
Centre Interdisciplinaire de Recherche en Réadaptation et Intégration Sociale
Québec, Quebec, Canada
Countries
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Related Links
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pubmed Canada study results
Other Identifiers
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CDHA-RS/2012-133
Identifier Type: OTHER
Identifier Source: secondary_id
230378
Identifier Type: -
Identifier Source: org_study_id
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