Clinical Trial

Time-Restricted Eating After Bariatric Surgery

Recruiting
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Summary
This study aims to compare the effects of time-restricted eating (TRE, 16/8) in adults with obesity who have and have not undergone bariatric surgery (BS). The study will include adults aged 18-65 years: those with obesity who have not undergone BS, and those who have experienced insufficient weight loss (IWL) or weight regain (WR) following BS. Both groups will follow a 16:8 time-restricted eating protocol for 6 weeks, with an 8-hour eating window recommended between 10:00 AM and 6:00 PM, though participants may adjust to other 16-hour fasting windows. Participants will be evaluated before and after the intervention in terms of anthropometric measurements, biochemical parameters, and dietary habits. The study is being conducted at a private hospital in Bursa, Turkey, and is planned to be completed with a total of 40 participants (20 per group).
Trial Details
NCT Number NCT07672821
Lead Sponsor Medipol University
Conditions Obesity & Overweight, Bariatric Surgery, Weight Regain, Weight Regain Post Bariatric Surgery, Time Restricted Feeding
Enrollment 40 participants
Start Date 2025-07-12
Primary Completion 2026-06 (estimated)
Study Completion 2026-07-12 (estimated)
Updated on ClinicalTrials.gov 2026-06-29