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Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy

Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07658326
Acronym
Tendistress
Enrollment
100
Registered
2026-06-22
Start date
2023-09-28
Completion date
2026-09-01
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress, Tendinopathy Rotator Cuff

Brief 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.

Interventions

OTHERQuestionnaires

MSP9 score Cungi scale EVA scale

Sponsors

GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Stress will be assessed using the MSP9 score.PreoperationThis 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

Countries

France

Contacts

CONTACTJean-François Oudet
jf.oudet@ecten.eu0033683346567
CONTACTMarie-Hélène Barba
mh.barba@ecten.eu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026