Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07086716

Frailty in Hip or Knee Arthroplasty Patients.

The Role of Frailty in the Rehabilitation Pathway Following Hip or Knee Arthroplasty Surgery.

Status
Recruiting
Phase
Study type
Observational
Enrollment
124 (estimated)
Sponsor
Joel Pollet · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study aims to understand the existing differences between frail and non-frail subjects who underwent a rehabilitation path after receiving hip or knee arthroplasty surgery.

Detailed description

This study wanted to investigate the role of frailty in the rehabilitation path following hip or knee arthroplasty. Subjects will be divided according to the type of arthroplasty received (i.e., hip or knee arthroplasty). Consequently, each arthroplasty group will be divided into a frail group and a non-frail group based on the presence of frailty conditions before receiving surgery. Frailty condition will be assessed using the Primary Care Frailty Index, based on the information reported in each patient's medical record before surgery. Frailty level will be reassessed during the rehabilitation period, specifically at hospitalization in the rehabilitation ward (T0) and Discharge (T1). While other time points considered for the primary outcomes will be at 3-month follow-up (T2) and 1-year follow-up (T3), alongside the primary and secondary outcomes chosen for the study. The different outcomes considered in this study were selected to provide a wide range of information regarding body structure and function, activity level, and perceived level of satisfaction with the intervention. Moreover, the long-term follow-up will collect data on the adverse event rate, which previous studies have shown to significantly impact more frail subjects after receiving arthroplasty. However, the possible protective role of rehabilitation has never been considered. This prospective case-control study is the first to consider the crucial role of rehabilitation in the post-surgical path of subjects receiving arthroplasties. It can serve as a preliminary basis for further trials based on tailored interventions for frail subjects.

Conditions

Timeline

Start date
2025-06-03
Primary completion
2027-01-01
Completion
2027-12-01
First posted
2025-07-25
Last updated
2025-07-25

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT07086716. Inclusion in this directory is not an endorsement.