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
This trial does not accept healthy volunteersQualifiers
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 population
Patients will be recruited from the orthopedic surgery department of the centers (Clinique de l'Union, Clinique la Croix du sud and Clinique des Cèdres).
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Questionnaires
Other interventionMSP9 score Cungi scale EVA scale
Treatment groups
100 Participants
are divided into 1 treatment groupGroup A: patient undergoing surgery for rotator cuff tendinopathy1 intervention
Trial outcomes
Primary outcomes
1
Stress will be assessed using the MSP9 score.
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
Time frame
PreoperationSponsors and contacts
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Source ClinicalTrials.gov