Time-Restricted Eating After Bariatric Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMedipol University

About this trial

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).

Eligibility criteria

Qualifiers

Adults aged 18-65 years with obesity who have not undergone bariatric surgery

Adults aged 18-65 years with obesity who have undergone bariatric surgery and experienced insufficient weight loss (IWL) within 18 months post-surgery, -defined as %EWL <50% at 18 months

Adults aged 18-65 years with obesity who have undergone bariatric surgery and experienced weight regain (WR), defined as >25% increase in %EWL from the lowest recorded weight

Disqualifiers

Pregnant or breastfeeding individuals

Acute illness, active infection, or comorbid conditions limiting treatment efficacy and safety, including: cancer, type 1 diabetes, renal or hepatic failure, recent stroke or myocardial infarction, nephrolithiasis, drug or alcohol abuse, eating disorders, severe depression or other psychiatric disorders, inflammatory bowel disease (IBD), neoplasia, arrhythmic heart disease, heart failure, respiratory failure, or corticosteroid therapy

Professional athletes

Trial design

Treatments tested in this trial

  • Time-Restricted Eating (16:8)

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Medipol University

Lead sponsor

Mudanya University

Sponsor institution