Actively Recruiting
The Role of Frailty in the Rehabilitation Pathway Following Hip or Knee Arthroplasty Surgery
Led by Joel Pollet · Updated on 2025-07-25
124
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the role of frailty in patients who have undergone hip or knee arthroplasty surgery and are now in rehabilitation. The study seeks to compare frail and non-frail subjects based on their recovery and outcomes following these surgeries. Frailty is assessed using the Primary Care Frailty Index from patient records before surgery, aiming to better understand how frailty affects rehabilitation and long-term results. Participants are grouped by the type of arthroplasty they received—hip or knee—and further divided into frail and non-frail groups. Frailty levels are reassessed at hospital admission for rehabilitation (T0) and at discharge (T1). Follow-up assessments will occur at 3 months (T2) and 1 year (T3) after surgery. The study collects various outcome measures including the Oxford Hip and Knee Scores, modified Barthel Index, pain rating scales, and adverse event rates to evaluate body function, activity, satisfaction, and safety. During the study, participants will undergo assessments at hospitalization, discharge, and follow-up visits up to one year post-surgery. These include clinical scores related to hip and knee function, pain levels, and rehabilitation progress. Researchers will monitor adverse events and use these data to understand the impact of frailty on recovery. This long-term observation aims to inform future tailored rehabilitation strategies for frail patients after arthroplasty.
CONDITIONS
Brief Title
Frailty in Hip or Knee Arthroplasty Patients.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Received elective hip or knee arthroplasty
- Ability to understand written and oral instructions
- Gave consent to study participation
You will not qualify if you...
- Arthroplasty revision or non-elective intervention
- Participation in other studies
- Hospitalized in rehabilitation ward more than 10 days after surgery
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.
1 visit (in-person)
Duration - Hospitalization or Day 1 to average Day 20
Participants undergo elective hip or knee arthroplasty surgery followed by initial hospitalization and post-operative care.
Hospital stay with daily assessments
Duration - Up to 1 year after surgery
Participants are monitored during the rehabilitation period and at scheduled follow-ups to assess recovery and frailty status.
Visits at discharge (around Day 20), 3 months, and 1 year after surgery
Trial Site Locations
Total: 1 location
1
Centro "E. Spalenza - Don Gnocchi
Rovato, BS, Italy, 25038
Actively Recruiting
Research Team
J
Joel Pollet, PT, MSc, PhD (s)
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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