Actively Recruiting
Multimodal Prehabilitation of Frail Patients 70 Years and Older Undergoing Elective Knee or Hip Replacement: A Pilot Randomized Controlled Trial
Led by University of Iceland · Updated on 2026-04-07
50
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
U
University of Iceland
Lead Sponsor
L
Landspitali University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Frailty is a common condition in older adults that reduces physical resilience and increases risks during surgery, especially for those undergoing hip or knee replacement. Researchers are evaluating a multimodal prehabilitation program to see if it can improve outcomes for frail patients aged 70 years and older who are scheduled for elective hip or knee arthroplasty. This pilot randomized controlled trial aims to provide early evidence on the program's feasibility and potential benefits. The study compares two groups: one receiving a multimodal prehabilitation program starting at least 2 months before surgery, and a control group receiving standard care. The prehabilitation includes a comprehensive geriatric assessment, medication review, tailored physiotherapy based on the Otago Exercise Programme, and nutritional counseling if malnutrition risk is detected. The control group follows usual preoperative routines, including physiotherapy guidance, nursing consultations, anesthetic evaluations, and medication adjustments, typically 1 to 4 weeks before surgery. Participants will be monitored from enrollment through surgery and up to 180 days afterward. Researchers will assess recruitment and retention rates, adherence to exercise and nutrition plans, physical performance using balance and mobility tests, postoperative complications, patient-reported joint health and quality of life, hospital stay length, discharge location, falls, readmissions, and mortality. This comprehensive evaluation aims to inform the design of larger studies and improve care for frail arthroplasty patients.
CONDITIONS
Brief Title
Multimodal Prehabilitation of Frail Patients Undergoing Elective Knee or Hip Replacement
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 70 years or older assigned to undergo hip or knee replacement at Landspítali University Hospital
- Scheduled for elective hip or knee replacement with a waiting period of at least 2 months before surgery
- Willing to participate, provide informed consent, and be randomized to either the prehabilitation or control group
You will not qualify if you...
- Patients who screen negative for all frailty screening tools
- Patients currently receiving active physiotherapy more than once a month
- Patients not undergoing planned surgery or those undergoing redo hip or knee prosthesis replacement
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 2 to 8 months
Participants undergo a multimodal prehabilitation program starting at least 2 months before planned surgery. This includes geriatric assessment, medication review, nutritional assessment if needed, and individualized physiotherapy with initial and follow-up sessions. Participants are encouraged to perform exercises at home multiple times per week.
Initial physiotherapy session with follow-up visits
Duration - Surgery day and immediate recovery period
Participants undergo elective hip or knee replacement surgery followed by immediate post-operative care.
Duration - 3 to 6 months
Participants are followed up for 3 to 6 months after surgery to assess changes in health status, quality of life, and functional tests.
Follow-up visits for assessment after surgery
Trial Site Locations
Total: 1 location
1
Landspitali University hospital
Reykjavik, Iceland, 101
Actively Recruiting
Research Team
M
Martin I Sigurdsson, MD, PhD
L
Luis G Rabelo, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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