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Life sciences · Interventional Study
ClinicalTrials.gov · September 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
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Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07826065). This is a study registration, not published results. Lead sponsor: TC Erciyes University. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 66 participants (ACTUAL). Conditions: Obesity & Overweight. Interventions: OTHER: 16:8 Time-Restricted Feeding and Exercise; OTHER: Standart Diet and Exercise. Primary outcome measures: Change in Fasting Blood Glucose , Baseline and 12 weeks; Change in HOMA-IR Index , Baseline and 12 weeks; Change in Lipid Profile Parameters , Baseline and 12 weeks; Change in Serum ALT Level , Baseline and 12 weeks; Change in Serum AST Level , Baseline and 12 weeks; Change in Body Mass Index (BMI) , Baseline and 12 weeks; Change in Body Weight , Baseline and 12 weeks; Change in Body Fat Percentage , Baseline and 12 weeks; Change in Total Cholesterol , Baseline and 12 weeks; Change in Triglycerides , Baseline and 12 weeks; Change in HDL Cholesterol , Baseline and 12 weeks; Change in LDL Cholesterol , Baseline and 12 weeks. Brief summary: This study was conducted to compare the effects of a 12-week 16:8 Time-Restricted Feeding (Intermittent Fasting) + home-based exercise protocol with and a calorie-restricted Standard Diet (SD) + home-based exercise protocol on body composition, lipid profile, glycemic control, and liver function enzyme levels in obese women.