The PREPARE Trial: Exercise Before Surgery to Improve Recovery in Older People With Frailty
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- STATUS
- Recruiting
-
- participants needed
- 750
-
- sponsor
- Ottawa Hospital Research Institute
Summary
This study evaluates whether participating in a home-based exercise program leads to lower
levels of
Description
Background: Four out of ten older people having
Despite frailty's strong association with adverse outcomes, few perioperative trials include
older people with frailty.
Research aims: Estimate the effectiveness of exercise
- Co-primary outcomes: patient-reported disability 30-days after
surgery and in-hospital complications - Secondary outcomes: patient-centered (discharge home, survival, 30, 90 and one-year disability scores, quality of life, function) and system-relevant (length of stay, admissions)
- Health economic outcomes: costs, cost-effectiveness
- Methods
Design, setting and participants: Parallel-arm multicenter randomized controlled trial at 14
Canadian hospitals. People => 60 years old with frailty (Clinical Frailty Scale score of 4/9)
having major elective non-cardiac
Intervention: Home-based exercise program with demonstrated efficacy, feasibility and acceptability tailored for people with frailty.
Outcomes and sample size: Co-primary outcomes are patient-reported disability 30 days after
Expertise: Our team features multidisciplinary clinical and methodological experts, nationally representative knowledge users and patient representatives.
Expected outcomes: Older people with frailty are a growing and vulnerable segment of the
surgical population and are under-represented in existing studies. Exercise
Details
Condition | Frailty, Surgery--Complications, Disability Physical |
---|---|
Age | 60years - 100years |
Treatment | Exercise Group |
Clinical Study Identifier | NCT04221295 |
Sponsor | Ottawa Hospital Research Institute |
Last Modified on | 19 February 2024 |
How to participate?
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1 study centers available
The Ottawa Hospital
Ottawa ON Canada
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The Ottawa Hospital
Ottawa ON Canada
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Ivy Salter
Primary Contact
The Ottawa Hospital
Ottawa ON Canada
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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