Self-efficacy Clinical Trial
Official title:
A Feasibility Study to Evaluate and Refine a Manual Wheelchair Training Program That is Enhanced for Self-efficacy(WheelSee): A Pilot Controlled Trial
Self-efficacy predicts behavioural and rehabilitation outcomes and may be an important psychological factor for wheelchair mobility. A feasibility study will evaluate a novel self-efficacy enhanced wheelchair training intervention (WheelSee) to determine if: 1.WheelSee improves self-efficacy compared to standard care; 2. study design is appropriate; and 3. The WheelSee intervention protocol is suitable. This feasibility study will allow for study design and protocol refinement and will provide pilot data for an experimental trial.
The purpose of this study is to evaluate the feasibility of administering a novel
self-efficacy enhanced wheelchair training intervention (WheelSee) for manual wheelchair
users who are at least 19 years of age. Self-efficacy for wheelchair use is an important
construct, which may influence wheelchair mobility and participation. Pilot data obtained
from this study will inform the design of an experimental trial and refinement of the
WheelSee intervention and protocol.
This study will use a randomized controlled, single blind design with a sample of 24 (12
intervention, 12 control). Participants will be randomly allocated to the intervention or
control group using a computer generated table of random numbers. Participants allocated to
the intervention group will take part in WheelSee in groups of 2-4. The WheelSee intervention
consists of 6 (twice weekly, minimum 3 days apart) x 1.5 hour sessions. Participants will be
encouraged to bring a family member to each session, who may act as a spotter during the
practice of wheelchair skills. If no family member is available, a student volunteer spotter
will be available to ensure a 1:1 spotter: wheelchair user ratio. All spotters will be
trained in appropriate spotting techniques.
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