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NCT06804044Completed

Intermittent Fasting (IF) Has Gained Recognition as a Promising Weight Loss Approach That Improves Body Weight, Insulin Resistance, and Metabolism. While Standard Diets Are Common in PCOS Management, IF May Address the Underlying Causes of Weight Gain and Offer Additional Metabolic Benefits

Effects of Different Dietary Programs on Anthropometric Parameters in Women With Polycystic Ovary Syndrome

Source: ClinicalTrials.gov · Last updated 31 Jan 2025

Brief summary (registry, in English)

The goal of this clinical trial is to learn if dietary interventions works to improve anthropometric measures in women with PCOS. The main questions it aims to answer are: * Does intermittent fasting (IF) cause loss of body weight, fat and muscle mass? * Can IF be considered more effective to medical and standart nutrition therapy (SDT)? * What dietary problems do participants have when having IF diet? Participants will: * Follow IF, SDT, or no intervention for 8 weeks. * Visit the clinic once every 2 weeks for check ups with a total of 5 visits for intervention groups IF and STD, visit at the beginning, second week and at the end for control group * Keep dietary records

Status (registry)
Completed
Study type
Interventional
Enrollment
33 (actual)
First submitted
21 Jan 2025
Start date
30 Nov 2022
Primary completion date
30 May 2023
Lead sponsor
Bahçeşehir University
NCT number
NCT06804044

What you commit to

  • Study type: Interventional
  • Participants enrolled: 33
  • From 30 Nov 2022 to the primary completion date, 30 May 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Women using medication,

Other illness

  • An endocrine disorder other than polycystic ovary syndrome
  • Chronic liver and kidney disease,
  • Diabetes,
  • Hypertension,
  • Heart Failure,
  • Thyroid disease,
  • Individuals with psychiatric disorders,
  • Oncological diseases,

Other

  • Hyperuricemia,
  • Pregnant and breastfeeding women,
  • Those with pacemakers and platinum,
  • Those with special nutritional needs

Who the study is looking for

  • Voluntariness to participate in the study
  • BMI between 25-35 kg/m2
  • Women between the ages of 18-45

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bahçeşehir University
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.