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Life sciences · Interventional Study
ClinicalTrials.gov · October 7, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT06951893). This is a study registration, not published results. Lead sponsor: Centre Hospitalier Metropole Savoie. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 165 participants (ESTIMATED). Conditions: Obesity, Morbid, Obesity and Overweight, Bariatric Surgery, Bariatric Surgery Patients, Bariatric Surgery Patient, Bariatric Surgery (Sleeve Gastrectomy ), Bypass, Gastric. Interventions: OTHER: Hospital Anxiety and Depression Scale; OTHER: Dutch Eating Behaviour Questionnary; OTHER: Impact of Weight on Quality Of Life; OTHER: body schema; OTHER: body mass index; OTHER: waist size. Primary outcome measures: Time trajectories of EQVOD score during the 24 months post-surgery from measurements at M12, M18 and M24 according to phenotypic characteristics measured during the final pre-surgical assessment (M-1 of bariatric surgery) , one month befre surgery to 24 month post surgery. Brief summary: This study aims to identify pre-operative phenotypic determinants predictive of quality of life trajectories in post-bariatric surgery patients. In addition, this study will have as a secondary objective the highlighting of a potential link between post-surgery quality of life trajectories and those of anxiety/depression scores, eating behaviors and body mass indices. This study will be conducted during the usual care of patients undergoing the GEROM73 program, lasting a total of 30 months. The GEROM73 program includes care for the six months preceding bariatric surgery and the 24 months following surgery. This program supports patients throughout their bariatric care.. Throughout the GEROM73 program, patients will complete questionnaires on anxiety, depression, eating disorders, Impact of Weight on Quality Of Life. Patients' weight, body mass index and body schema will also be measured throughout the GEROM program.