Preoperative Stress Levels in Shoulder Tendinopathy Surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects questionnaires from adults undergoing first-line shoulder surgery for rotator cuff tendinopathy to measure their stress before surgery. It aims to see if higher preoperative stress correlates with longer or more difficult postoperative recovery. The design relies on questionnaire data without an experimental intervention. Results could help identify whether psychological factors are associated with postoperative outcomes in shoulder surgery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient, male or female, over 18 years of age
* First-line surgery for rotator cuff tendinopathy (torn and untorn)
* Subject affiliated with or covered by a social security scheme
* Collection of the patient's non-opposition to participate in the study

Exclusion Criteria:

* Patients with medical history of adhesive capsulitis or complex regional pain syndrome (CRPS)
* Patients with a history of diabetes or thyroid dysfunction
* Patients with a history of fibromyalgia
* Patients with a history of mental illness (PMD, schizophrenia)
* Patients taking antidepressants or similar medications
* Patients participating in another clinical trial
* Protected patients: adults under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative decision;
* Pregnant, breastfeeding, or parturient women;
* Patients hospitalized without their consent.

Where it's running

• Clinique des Cèdres
  Cornebarrieu, France Recruiting
• Clinique la croix du sud
  Quint-Fonsegrives, France Recruiting
• Clinique de l'Union
  Saint-Jean, France Recruiting

Study contacts

• Study coordinator: Jean-François Oudet
• Email: jf.oudet@ecten.eu
• Phone: 0033683346567

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.