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New rehab tackles fear of movement after shoulder surgery

NCT ID NCT06154889

Symptom relief Sponsor: Clinique Générale dAnnecy Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether adding psychological support to standard physical therapy can reduce fear of movement (kinesiophobia) in people who have had shoulder stabilization surgery for recurrent dislocations. 52 participants will be randomly assigned to either standard rehab or a new program that includes consultations with a sports psychologist. The goal is to improve quality of life and return to sport.

What this could mean

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

Active substance
rehabilitation protocol with psychological counseling
What this could lead to
If successful, this could lead to a standard rehab program that helps people return to sports and daily activities with less fear after shoulder surgery.
What could go wrong
This is a small, early-stage study with only 52 participants, so results may not apply to everyone. The psychological component may not significantly improve outcomes over standard rehab.

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 52 people

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

Started

Nov 2023

Expected to finish

May 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 to 67 years

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: 1. Primary or recurrent traumatic anterior dislocation of the shoulder 2. Indication of abutment according to Latarjet (arthroscopic or open sky) 3. Age: 18-67 years 4. Understanding of the French language spoken and written 5. Written informed consent (in accordance with to ICH-GCP guidelines) Exclusion Criteria: 1. Posterior or multidirectional instability of the shoulder (Beighton score \>5) 2. Age \<18 or \>67 years. 3. Patients with additional rotator cuff tear. 4. Patients with a history of surgery on either shoulder. 5. Patients with connective tissue disorders (eg Ehler-Danlos). 6. Patients with (current) anxiety disorders or using anxiolytic medications (eg, antipsychotics) (criterion based on patient record/indications). 7. Patients with neurological disorders or systemic disease. 8. Patients with inflammatory disease, rheumatoid arthritis or active malignancy. 9. Patients previously hospitalized for shoulder pain 10. Patients with upper tubercle fracture 11. Patients with motor neurological deficit 12. Pregnant or breastfeeding patient 13. Patient protected under protective measure

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Conditions

The condition(s) this trial relates to.

Kinesiophobia Shoulder Dislocation

As listed by the trial registrant

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

Dislocation shoulder

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

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Clinique Générale d'Annecy

    RECRUITING

    Annecy, 74000, France