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Hip Arthroplasty, TotalDigihipNCT06780319

Digital Rehabilitation After Hip Arthroplasty: a Randomized Controlled Trial

A study testing Standard rehabilitation and Tele-rehabilitation in people with Hip Arthroplasty, Total, run by Clinique du Sport, Bordeaux Mérignac at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Hip Arthroplasty, Total
What is being tested?
Standard rehabilitation and Tele-rehabilitation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteFrance
Study dates
4 Jun 2025to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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 locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Pierre Laboudie, MD contact

+33671270463

pierre.laboudie@gmail.com

France1 site, 1 recruiting
  • Clinique du Sport

    Mérignac, 33700

    Pierre Laboudie, MD, +33 (0)5 56 18 17 10, secretariatdrlaboudie@gmail.com

    Recruiting

Other trials in France

About this study

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.

Being tested
Standard rehabilitation, Tele-rehabilitation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Standard rehabilitationProcedure or surgery

    rehabilitation with a private physiotherapist. Patients usually undergo 15 rehabilitation sessions, in line with HAS recommendations; the number of sessions can go up to 25, depending on the patient's profile and needs.

  • Tele-rehabilitationProcedure or surgery

    Tele-education is a digital home-based intervention involving exercises and education. Patients are monitored remotely by a physiotherapist via a secure messaging system. The system consists of a mobile application for the patient and a web portal enabling the physiotherapist to review patient data (physical activity, pain levels, medication use, exercise adherence, patient-reported results, images, videos) on a daily basis and tailor the protocol accordingly.

Study groups in NCT06780319
Study groupRoleWhat they receive
standard rehabilitationActive comparatorNot described
Receives: Procedure: Standard rehabilitation
Tele-rehabilitationExperimentalNot described
Receives: Procedure: Tele-rehabilitation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time Up and Go test

    The TUG is a clinical test used to assess patients' mobility and risk of falling. It measures the time required for a person to stand up from a chair, walk a short distance, turn around, return to the chair and sit down.

    Measured: 6 weeks and 6 months after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Jan 2025
  2. Study start4 Jun 2025
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06780319
Sponsor's protocol ID
2024-17-SBM
Acronym
Digihip
Status last verified
Jul 2026
First submitted
13 Jan 2025
Last updated
9 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Standard rehabilitation and Tele-rehabilitation in people with Hip Arthroplasty, Total, run by Clinique du Sport, Bordeaux Mérignac at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 9 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pierre Laboudie, MD (+33671270463, pierre.laboudie@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Time Up and Go test (time frame: 6 weeks and 6 months after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jul 2026.

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