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Recruiting Observational

Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy

NCT07658326 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-09-28
Last updated
2026-07-16

Condition(s) studied

StressTendinopathy Rotator Cuff

Investigational drug(s) / intervention(s)

Questionnaires

Questionnaires: MSP9 score Cungi scale EVA scale

Study summary

Orthopedic surgery of the limbs presents a unpredictable postoperative course, which can be more or less lengthy in terms of functional recovery and resumption of personal or professional activities. Not uncommon, convalescence can require many months with dramatic personal and/or socio-professional consequences (disability, unemployment, etc.), particularly in the postoperative development of complex regional pain syndrome (CRPS) and/or adhesive capsulitis.

Among the suspected contributing factors, the existence of an unfavorable preoperative psychological context in patients is often mentioned.

This research is based on the hypothesis that a high level of preoperative stress in patients could contribute to the occurrence of more significant postoperative complications in patients who have undergone shoulder surgery.

The main objective is to measure the level of preoperative stress in patients undergoing surgery for rotator cuff tendinopathy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

  • Stress will be assessed using the MSP9 score. — Preoperation
    This score ranges from 9 to 72 based on a rating scale of 1 to 8 (reversed for positive items): * 9-26 - Very low stress level * 27-44 - Low stress level * 45-54 - Moderate stress level * 55-63 - High stress level * 64-72 - Very high stress level

Trial sites (3)

FacilityCityRegionStatus
Clinique des Cèdres Cornebarrieu France Recruiting
Clinique la croix du sud Quint-Fonsegrives France Recruiting
Clinique de l'Union Saint-Jean France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07658326 on ClinicalTrials.gov ↗ ← All trials in France