Clinical Trial

Impact of a Perioperative Physical Exercise and Respiratory Physiotherapy Program on the Patient Undergoing Bariatric Surgery

Study acronym: CAPS-OB
Recruiting
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Summary
The goal of this clinical trial is to see the impact of a physical exercise programme and respiratory physiotherapy before and after bariatric surgery in obese patients. The main questions it aims to answer are: Could it help to avoid decompensation of underlying diseases? Could it reduce the risks associated with the intervention and the number of adverse effects during the postoperative period? Could it reduce the number of patients and encourage early discharge? How does exercise affect epigenetics in obese patients undergoing bariatric surgery? Can we correlate epigenectic markers obtained from tissue obtained by invasive procedures such as fat or muscle to those obtained by non-invasive methods such as blood and saliva samples? How does exercise affect the hepatic tissue in obese patients undergoing bariatric surgery? And are the any predictive markers in pre-exercise samples that can correlate with the evolution of liver diseases such asl NALFD or NASH? Researchers will compare one group of subjects performing the exercise programme and respiratory physiotherapy and anoher group performing the normal activities of routine clinical practice. Participants, who are on the surgical waiting list for bariatric surgery, will be assigned to one of the two groups. Participants in group 2 will follow the normal procedure before and after surgery. Participants in group 1 will be asked to do a exercise programme and respiratory physiotherapy before and after surgery.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2026-05-07 -> 2028-09-30 2026-07-25
minor Completion pushed: 2026-09-07 -> 2028-12-30 2026-07-25
Trial Details
NCT Number NCT06987903
Lead Sponsor Fundacin Biomedica Galicia Sur
Conditions Bariatric Surgery and Physical Activity, Obesity/Therapy, Bariatric Surgery Complications, Bariatric Patients
Enrollment 132 participants
Start Date 2025-05-07
Primary Completion 2028-09-30 (estimated)
Study Completion 2028-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-24