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Pre-surgery rehab and app-based follow-up may calm nerves after ACL repair

NCT ID NCT06099600

Symptom relief Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time

Summary

This trial tests whether a short pre-habilitation stay (rehab before surgery) combined with digital follow-up via a smartphone app can reduce anxiety one week after anterior cruciate ligament (ACL) reconstruction, compared to standard care. Adults with a partial or complete ACL tear scheduled for surgery are eligible. The study measures anxiety using a standard questionnaire.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
a pre-habilitation stay (in-person rehab before surgery) plus digital follow-up via a mobile app
What this could lead to
If effective, this approach could reduce post-surgery anxiety and improve recovery for people undergoing ACL reconstruction.
What could go wrong
This is a small, early-stage trial. The benefits may be modest or not generalizable to all patients. Digital follow-up requires reliable internet and device access.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 84 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2025

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age\>18; * Partial or complete tear of the anterior cruciate ligament; * Scheduled anterior cruciate ligament reconstructive surgery; * Patient with a tablet, computer or smartphone with an internet connection; * Patient able to understand and read French; * Willingness to complete questionnaires at regular intervals; * Membership of a social security scheme; * Signed informed consent. Exclusion Criteria: * History of anterior cruciate ligament surgery within the past 5 years; * Stage III collateral ligament injury; * Osteotomy; * Neurological (motor and/or sensory), vestibular or rheumatic pathology; * Pregnant or breast-feeding woman; * Protected adult patient (under guardianship, curatorship or deprivation of liberty).

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Ligament rupture

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Clinique de la Sauvegarde

    RECRUITING

    Lyon, 69009, France

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