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Completed NCT07651254

Effects of a 12-week Supervised Exercise Program Post Bariatric Surgery on Body Composition, Muscle Strength, and Insulin Resistance

Conditions: Bariatric Surgery, Exercise, Body Composition Changes

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 61
Sponsor: Laval University

Location: Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval Québec Quebec

Summary

The goal of this clinical trial is to evaluate the impact of supervised training program on body composition, muscular strenght, insulino-resistance profile, heart rate variability and on heart structure and function between 3 to 6 months after mixed bariatric surgery or restrictive bariatric surgery. This study will be conducted in men and women with severe obesity. Respectively for each type of surgery (mixed vs. restrictive), participants will be randomized either to the exercise group or to the control group. For participant randomized in the exercise group, 3 months after the bariatric surgery, they will started a supervised exercise program for 3 months. In contrast, for participant randomized in the control group, they will have consultation with kinesiologist to receive general information about physical activity practice. Each participants will perform 4 evaluations; one before bariatric surgery and 3 after bariatric surgery (3 months, 6 months and 12 months). Thoses evaluations will be assessed at each visit : fasting blood draw, anthropometric measurements, cardiac echocardiography, heart rate variability measurement, mid-thigh and abdominal computed tomography scan, maximal exercise test, six-minute walk test, assessment of lower-limb endurance and strength, assessment of physical activity level and energy expenditure.

Eligibility Criteria

Inclusion Criteria: * Be 18 years and older * Have a weight lower than 200 kg * Interested in participating in a supervised training program Exclusion Criteria: * Having undergone a vagotomy * Having undergone a bariatric surgery * Having used orlistat in the past three months * Having a major cognitive imparment that may limit adherence to study visits * Having a pacemaker * Having a total hip replacement * Being claustrophobic

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07651254). StuddyBuddy aggregates publicly available trial information.