Actively Recruiting
Frailty Rehabilitation
Led by McMaster University · Updated on 2025-07-06
324
Participants Needed
1
Research Sites
173 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Frailty is an important clinical state that contributes to falls, hospitalization, institutionalization and death. When an individual simultaneously has many health problems, a frailty "tipping point" may be triggered by even a minor stressful event such as adding a new drug or urinary tract infection. Our research suggests that approximately 23% of Canadians over age 65 are frail, and by age 85 this estimate increases to over 40%. As we learn more about frailty and its consequences, there is an urgent need to develop community-based interventions that will prevent or delay frailty in older adults. Our proposed study will examine if frailty rehabilitation program is an effective community-based intervention to promote healthy aging. The primary objective of our study is to determine if 4-month frailty rehabilitation improves physical function compared with control and exercise alone in community-dwelling older adults living with frailty and sarcopenia. Secondary objectives of our study are to determine if 4-months of frailty rehabilitation can improve functional abilities and reduce healthcare utilization during a 6-month follow-up period compared with control and exercise alone. Results will translate the first Canadian model of frailty and sarcopenia rehabilitation and management.
CONDITIONS
Official Title
Frailty Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Community-dwelling adults aged 65 years or older
- Able to independently walk 25 meters with or without a walking aid
- At high risk for mobility disability or functional limitations
- Received medical clearance to participate
- Able to arrange transportation to YMCA up to twice per week
- Proof of full COVID-19 vaccination and identification
You will not qualify if you...
- Unable to speak or understand English
- Currently attending a group exercise program
- Currently enrolled in a drug optimization study or program
- Taking protein supplements daily
- Significant cognitive impairment affecting ability to follow two-step commands
- Receiving palliative or end-of-life care
- Diagnosed with unstable angina or heart failure
- Unable to attend more than 80% of the trial sessions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
McMaster University - St. Peter's Hospital
Hamilton, Ontario, Canada, L8M1W9
Actively Recruiting
Research Team
S
Sherri Smith
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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