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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RECRUITING
NA
100 participants
INTERVENTIONAL
2023-10-11
2026-12-31
Brief Summary
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Participants will be allocated to either a 10-week seated exercise program or a delayed 2-week Boot Camp program. All seated exercises sessions and assessments will be conducted virtually.
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Detailed Description
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Participants will use their own computer, laptop, or tablet for the zoom sessions. No Zoom sessions will be recorded. Caregivers will be invited to attend each exercise session to provide support and assistance but are not obliged to attend. A caregiver, friend, or family member will be required for each assessment to participate in the study.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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10-week group
Will receive a 10-week seated exercise program, occurring 3 times per week. Sessions will be 60 minutes in duration.
Virtual Physical Activity Seated Exercises (V-PASE)
The seated exercise program includes a variety of upper and lower limb strengthening, core strengthening, agility (fast arm and leg movements), and flexibility exercises. Participants will be supervised during each session thru videoconferencing by a trained instructor.
Delayed 2-week group (Boot Camp)
The Boot Camp group will complete a 2-week seated exercise program following the 10-week active trial period.
No interventions assigned to this group
Interventions
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Virtual Physical Activity Seated Exercises (V-PASE)
The seated exercise program includes a variety of upper and lower limb strengthening, core strengthening, agility (fast arm and leg movements), and flexibility exercises. Participants will be supervised during each session thru videoconferencing by a trained instructor.
Eligibility Criteria
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Inclusion Criteria
* Chronic stroke (more than 6 months post-stroke)
* Ability to stand up from a chair
* Mobility impairment of lower extremity (requires a walking aid, with or without close supervision)
* Able to safely engage in exercise and tolerate 60 minutes of exercises
* Able to communicate in English
* Have access to a tablet, computer, or laptop with internet and email access
Exclusion Criteria
* Participating in formal exercise or rehabilitation activities
* Participating in \> 30 minutes/day of physical activity (moderate intensity)
* Participating in another study that may affect outcomes to this study
* Severe loss of vision, hearing, speech (including aphasia) or cognition that would preclude use of a computer/tablet and communication over videoconference software
* A serious comorbid condition (eg., amputation, Parkinson's disease, active cancer)
* Clinically diagnosed with acute/chronic illness or other condition which has known physical activity contraindications or limits their ability to complete each experimental condition (i.e., chronic low back pain aggravated by prolonged sitting)
18 Years
ALL
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
Michael Smith Foundation for Health Research
OTHER
University of British Columbia
OTHER
Responsible Party
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Janice Eng
Professor
Locations
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GF Strong Rehabilitation Centre
Vancouver, British Columbia, Canada
University of Manitoba
Winnipeg, Manitoba, Canada
Nova Scotia Health
Halifax, Nova Scotia, Canada
Western University
London, Ontario, Canada
University of Saskatchewan
Saskatoon, Saskatchewan, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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H22-02549
Identifier Type: -
Identifier Source: org_study_id
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