Actively Recruiting
Stronger At Home: Improving Outcomes for Older Adults After Hip Fracture
Led by Dr. Mohammad Auais, PhD · Updated on 2025-03-21
200
Participants Needed
1
Research Sites
249 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare the effectiveness of a new 14-week individually-tailored home-based rehabilitation program called "Stronger at Home" with usual care in improving functional recovery in community-dwelling older adults after hip fractures. The main question this trial aims to answer are: • Is the Stronger at Home program more effective than usual care in improving functional recovery at the end of the 14-week intervention? secondary questions include: * What is the cost-utility of the Stronger at Home program compared to usual care at 3.5 months, 6 months, and 12 months after discharge? * Does the program have a sustained impact on functional recovery at 6 months and 12 months post-discharge? Participants in the trial will be asked to engage in the following tasks: * Participate in the Stronger at Home program, which includes using a self-directed toolkit consisting of educational resources and an illustrated exercise program. * Follow the guidelines provided in the toolkit for gradually increasing exercise intensity and incorporating different types of exercises into their daily life. The effects of the Stronger at Home program will be compared to those of usual care.
CONDITIONS
Official Title
Stronger At Home: Improving Outcomes for Older Adults After Hip Fracture
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hip fracture patients who are 55 years or older
- Currently living in the community
- Being discharged to their home or a retirement home
- Hip fracture caused by a fall from standing height or less
- Living within 45 km radius of the recruitment site
You will not qualify if you...
- Came from long term care or discharged to long term care
- Fracture is not a hip fracture (e.g., pelvic fracture)
- Unable to give consent and no proxy available
- Fracture due to pathological disease (e.g., cancer, Paget's disease)
- Does not speak English and has no translator
- Fracture sustained at the hospital
- Has a terminal illness or contraindications to exercise
- Discharged with other services that are not eligible
AI-Screening
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Trial Site Locations
Total: 1 location
1
Queen's University
Kingston, Ontario, Canada, K7L 3N6
Actively Recruiting
Research Team
M
Mohammad Auais
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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