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Digital Rehabilitation After Hip Arthroplasty: a Randomized Controlled Trial (Digihip)

C

Clinique du Sport, Bordeaux Mérignac

Status

Enrolling

Conditions

Hip Arthroplasty, Total

Treatments

Procedure: Standard rehabilitation
Procedure: Tele-rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT06780319
2024-17-SBM

Details and patient eligibility

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.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have an email address and a smartphone
  • Patient speaking and writing French
  • Patient covered by a social security scheme

Exclusion criteria

  • Hip revision surgery, significant comorbidities (Parkinson's disease, multiple sclerosis, stroke) or psychiatric disorders (substance use) that could interfere with rehabilitation
  • Patients with disorders that make it difficult for them to express their feelings
  • Pregnant or breast-feeding patients
  • Patient under protective supervision
  • Patient not covered by a social security scheme

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

standard rehabilitation
Active Comparator group
Treatment:
Procedure: Standard rehabilitation
Tele-rehabilitation
Experimental group
Treatment:
Procedure: Tele-rehabilitation

Trial contacts and locations

1

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Central trial contact

Pierre Laboudie, MD

Data sourced from clinicaltrials.gov

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