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The Effects of the Mediterranean Diet and Synbiotics in Polycystic Ovary Syndrome

A

Atlas University

Status

Not yet enrolling

Conditions

PCOS (Polycystic Ovary Syndrome)

Treatments

Dietary Supplement: Synbiotic Supplement
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT07342946
E-22686390-050.99-78501

Details and patient eligibility

About

This study will look at whether a reduced-calorie Mediterranean-style eating plan, together with a synbiotic supplement, can improve health measures and quality of life in women who have polycystic ovary syndrome (PCOS) and are overweight or have obesity. Participants will be assigned by chance (like flipping a coin) to receive either the synbiotic supplement or a placebo (a look-alike product with no active ingredients). All participants will follow the same reduced-calorie Mediterranean diet for 8 weeks. The study team will measure body composition and weight-related measurements, and will collect blood samples to evaluate selected laboratory markers before and after the 8-week period. Participants will also complete the PCOSQ-50 quality-of-life questionnaire before and after the intervention. The goal is to better understand the possible role of synbiotic supplementation alongside dietary treatment in PCOS.

Full description

This randomized, placebo-controlled, single-blind clinical trial is designed to evaluate the effects of a hypocaloric Mediterranean diet combined with synbiotic supplementation on anthropometric measurements, biochemical parameters, and quality of life in overweight and obese women diagnosed with polycystic ovary syndrome (PCOS). Eligible participants will be randomly assigned to one of two study arms: a synbiotic supplementation group or a placebo group. Both groups will follow the same hypocaloric Mediterranean diet throughout the 8-week intervention period.

Anthropometric assessments, including body weight, body mass index, waist circumference, and body composition, will be performed at baseline and at the end of the intervention. Biochemical parameters will be evaluated through blood samples collected at baseline and after 8 weeks. Quality of life will be assessed using the PCOSQ-50 Quality of Life Questionnaire at both time points.

The study aims to determine whether the addition of synbiotic supplementation to a hypocaloric Mediterranean diet provides additional benefits in the management of PCOS-related metabolic parameters and quality of life compared with dietary intervention alone.

Enrollment

32 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Premenopausal women who are overweight or obese, with a body mass index (BMI) between 25 and 35 kg/m²
  • Aged 18 to 45 years (reproductive age)
  • Diagnosed with polycystic ovary syndrome (PCOS)

No underlying metabolic diseases, including type 2 diabetes mellitus, hypertension, diagnosed anemia, or any other metabolic condition requiring a special diet

Exclusion criteria

  • Pregnancy or breastfeeding within the past 6 months
  • Presence of comorbid conditions, including kidney, liver, or cardiovascular disease, gout, hyperuricemia, or other related disorders
  • Use of oral contraceptives
  • Following a special dietary treatment or a hypocaloric diet within the last 3 months
  • Occasional or current use of medications that may affect fluid balance, including diuretics and laxatives
  • Participants will be withdrawn from the study in case of abnormal biochemical parameters, non-adherence to the prescribed diet, or failure to comply with the supplementation protoco

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Participants in this arm will receive a hypocaloric Mediterranean diet in addition to a placebo for a period of 8 weeks.
Treatment:
Other: Placebo
Synbiotics
Active Comparator group
Description:
Participants in this arm will receive a hypocaloric Mediterranean diet in addition to synbiotic supplementation for a period of 8 weeks.
Treatment:
Dietary Supplement: Synbiotic Supplement

Trial contacts and locations

0

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Central trial contact

Ayşenur Emirhuseyinoglu-Calik

Data sourced from clinicaltrials.gov

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