Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRamsay Générale de Santé
About this trial
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 criteria
Qualifiers
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
Disqualifiers
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)
Trial design
Treatments tested in this trial
- Questionnaires
Treatment groups
100 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov