- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01644292
Enhancing Participation In the Community by Improving Wheelchair Skills: Phase 2 (EPIC WheelS)
November 28, 2023 updated by: University of Manitoba
Enhancing Participation In the Community by Improving Wheelchair Skills (EPIC WheelS): Phase 2
The purpose of this project is to conduct a pilot study of the EPIC WheelS wheelchair skills home training program for older adults in preparation for a third phase feasibility study.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Many older adults rely on a manual wheelchair for community mobility but are not provided with skills for independent and effective use.
Suboptimal or disuse of the wheelchair results in substantial social costs such as reduced engagement in meaningful activity, social isolation, and higher caregiver burden.
This represents a poor use of financial resources, including the cost of wheelchair acquisition and demands for attendant care.
Access to skills training is constrained by the cost and limited availability of skilled therapists, the demands of patient and clinician travel, and lack of programs designed specifically for the needs of older adults.
Enhancing Participation In the Community by improving Wheelchair Skills (EPIC WheelS) is an individualized home-training program that optimizes learning for older adults while limiting the demands on expert clinician trainers.
It is delivered using a portable computer tablet that allows interactive learning, customized updating, and communication with an expert trainer.
A monitored, home program that is effective and efficient for older adults has potential application for other target groups as well, particularly those with limited access to rehabilitation services in rural and remote locations.
Study Type
Interventional
Enrollment (Actual)
2
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Manitoba
-
Winnipeg, Manitoba, Canada, R3E 0T6
- University of Manitoba
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- at least 50 years old
- live in the community within metropolitan Winnipeg
- self-propel a MWC (Manual Wheelchair) at least 1 hour per day
- use their MWC for mobility outside of the home
- have used a MWC for less than 2 years
Exclusion Criteria:
- cannot communicate and complete study questionnaires in English
- anticipate a health condition that contraindicates wheelchair training
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: EPIC Wheels Training Intervention
EPIC Wheels skills training program
|
EPIC WheelS is a user-centred program for wheelchair skills training that combines two structured 1-hour sessions with an expert trainer and four weeks of self-directed practice and training in the natural (home) environment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline in Wheelchair Skills Test (WST) 4.1 Capacity Score
Time Frame: Baseline and follow-up (1 month)
|
The WST is a structured assessment with 32 discrete mobility skills required to perform social roles in the community, each scored dichotomously as pass/fail.
The WST produces a total Skill Capacity score (0-100%) reflecting the number of skills safely passed.
|
Baseline and follow-up (1 month)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ed M Giesbrecht, PhD (Cand.), University of Manitoba
- Principal Investigator: William C Miller, PhD, University of British Columbia
- Principal Investigator: Janice Eng, PhD, University of British Columbia
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2012
Primary Completion (Actual)
March 1, 2013
Study Completion (Actual)
March 1, 2013
Study Registration Dates
First Submitted
July 13, 2012
First Submitted That Met QC Criteria
July 16, 2012
First Posted (Estimated)
July 19, 2012
Study Record Updates
Last Update Posted (Actual)
November 30, 2023
Last Update Submitted That Met QC Criteria
November 28, 2023
Last Verified
January 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- H2012:069
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.