Actively Recruiting
Digital Rehabilitation After Hip Arthroplasty: a Randomized Controlled Trial
Led by Clinique du Sport, Bordeaux Mérignac · Updated on 2025-06-11
60
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study aims to compare the effectiveness of tele-rehabilitation versus no physical therapy after total hip arthroplasty (THA) in improving patient-reported outcomes and functional recovery. THR is a common surgical procedure to relieve pain and improve function in patients with a variety of hip conditions. Traditional physical therapy is a standard component of the post-operative care pathway for PTH patients, but can be hampered by logistical obstacles. Tele-rehabilitation is emerging as a promising alternative, offering the potential to overcome these barriers and improve access to care. The study uses a prospective monocentric design with two arms and a follow-up time of 6 months. The primary objective is assessed using the Timed up and go Test (TUG), while secondary objectives include patient-reported outcome measures, patient satisfaction, healthcare utilization, and return to physical activity.
CONDITIONS
Official Title
Digital Rehabilitation After Hip Arthroplasty: a Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Have an email address and a smartphone
- Patient speaking and writing French
- Patient covered by a social security scheme
- Age between 18 and 80 years
You will not qualify if you...
- Hip revision surgery
- Significant comorbidities such as Parkinson's disease, multiple sclerosis, or stroke
- Psychiatric disorders including substance use
- Disorders that impair expression of feelings
- Pregnant or breast-feeding patients
- Patient under protective supervision
- Patient not covered by a social security scheme
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique du Sport
Mérignac, France, 33700
Actively Recruiting
Research Team
P
Pierre Laboudie, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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