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Comparison of Time-Restricted Intermittent Fasting Diet in Individuals With and Without Bariatric Surgery

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Nev Sağlık Grubu
RECRUITING
Bursa
Nev Sağlık Grubu
RECRUITING
Bursa
Contact Information
Primary
Seher Şen, Assistant Professor
seherdalli@gmail.com
+905393919700
Time Frame
Start Date: 2025-07-12
Estimated Completion Date: 2026-07-12
Participants
Target number of participants: 40
Treatments
Active_comparator: Arm 1: Adults with Obesity (Non-Bariatric)
Adults with obesity who have not undergone bariatric surgery. Will follow 16:8 TRE protocol for 6 weeks.
Experimental: Arm 2: Adults with Obesity (Post-Bariatric)
Adults with obesity who experienced insufficient weight loss or weight regain following bariatric surgery. Will follow 16:8 TRE protocol for 6 weeks.
Related Therapeutic Areas
Sponsors
Leads: Medipol University

This content was sourced from clinicaltrials.gov