Two Different Dietary Interventions for Girls With Polycystic Ovary Syndrome

March 3, 2023 updated by: Esra Döğer, Gazi University

Beneficial Effects of Resemena Diet on Anthropometric, Metabolic and Reproductive Profile in Adolescents With Obesity and Polycystic Ovary Syndrome: a Randomized Controlled Intervention Study

This study was conducted to evaluate the efficacy of the MEtabolic Syndrome REduction in NAvarra (RESMENA) diet versus a control diet based on American Heart Association (AHA) recommendations for the treatment of PCOS in adolescents with obesity and PCOS. A total of 40 adolescents diagnosed with PCOS between the ages of 13-18 years were randomized to either a Resmena or control diet for 6 months. Dietary status, anthropometry, body composition, biochemical parameters, and reproductive endocrine hormones were compared between the 2 groups before and after the intervention.

Study Overview

Detailed Description

The purpose of this study was to investigate the effect of a high meal frequency, low carbohydrate, high protein, high n-3 PUFA, healthy fatty acid and antioxidant content, low glycemic load Resmena diet or a control diet based on AHA recommendations on anthropometric measurements, body composition, insulin resistance, lipid metabolism levels, inflammatory markers and reproductive endocrine levels in adolescents with obesity and PCOS..Randomized controlled study design was used in the study. Patients in the study were allocated to the control and study intervention groups. Participants were invited to face-to-face interviews at the beginning of the study and monthly for 6 months.

Anthropometric measurements, body composition analysis, and a physical activity questionnaire were performed at the beginning and end of the study, and three-day food consumption records and blood samples for the measurement of biochemical parameters were collected. In addition, the physical activity and food consumption records of the participants were repeated in monthly controls and their anthropometric measurements and body composition were analyzed and compared.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey, 06500
        • Esra Döğer

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Diagnosis of PCOS in adolescent girls according to the Rotterdam criteria
  • Age 13-18 years,
  • Body mass index (BMI) ≥ 95th percentile

Exclusion Criteria:

  • Other endocrine etiological disorders (Cushing's syndrome, congenital adrenal hyperplasia, McCune Albright syndrome, mutations in the glucocorticoid receptor gene, ovarian and adrenal androgen-secreting tumors, hyperprolactinemia, diabetes mellitus, thyroid dysfunction, adrenal, and other endocrine disorders),
  • Cardiovascular and cerebrovascular diseases,
  • Hematologic disorders
  • Liver and kidney failure
  • Mental disorders
  • Eating disorders
  • Contraceptive use in the last 3 months
  • Use of insulin-sensitizing agents
  • Use of drugs affecting lipid metabolism (such as fish oil)
  • Smoking.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: İntervention group
METAbolic Syndrome REduction in NAvarra (RESMENA) diet was applied to adolescents with PCOS

The Resmena diet: It was characterized by a higher meal frequency, consisting of seven meals/d (including breakfast, lunch, dinner, and two snacks in the morning and two snacks in the afternoon), and by a different macronutrient distribution; 40% total energy value from CHO, 30% from proteins and 30% from lipids. This pattern tried to reinforce high n-3 polyunsaturated FA (n-3 PUFA) and high natural antioxidant food consumption and promoted low GL CHO intake as well as a high adherence to the Mediterranean diet. It also maintained a healthy FA profile and a cholesterol content of less than 300 mg/day.

  • Daily meal plans were created according to the energy intake of the participants and sent to the participants via social media every week. Participants were asked to keep 3-day diet records to evaluate their compliance with the diet and were invited to the research center once a month to be checked.
Experimental: conrol group
American Heart Association (AHA) guidelines based diet was applied to adolescents with PCOS

Control diet: It was based on the American Heart Association (AHA) guidelines, including 3-5 meals per day, a macronutrient distribution of 55% total energy value from carbohydrates, 15% proteins, and 30% lipids, a healthy fatty acids (FA) profile and a cholesterol consumption lower than 300 mg/day.

- Daily meal plans were created according to the energy intake of the participants and sent to the participants via social media every week. Participants were asked to keep 3-day diet records to evaluate their compliance with the diet and were invited to the research center once a month to be checked

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Luteinizing hormone (LH) (IU/L)
Time Frame: change between the first day and the sixth month of the study
Participants' serum LH levels was determined.
change between the first day and the sixth month of the study
Follicle-stimulating hormone (FSH) (IU/L)
Time Frame: change between the first day and the sixth month of the study
Participants' serum FSH levels was determined.
change between the first day and the sixth month of the study
Total and free (ng/mL)
Time Frame: change between the first day and the sixth month of the study
Participants' serum FSH levels was determined.
change between the first day and the sixth month of the study
Prolactin (ng/mL)
Time Frame: change between the first day and the sixth month of the study
Participants' serum prolactin levels was determined.
change between the first day and the sixth month of the study
Dehydroepiandrosterone sulfate (DHEA-S) (µg/dL)
Time Frame: change between the first day and the sixth month of the study
Participants' serum DHEA-S levels was determined.
change between the first day and the sixth month of the study
Androstenedione (ng/mL)
Time Frame: change between the first day and the sixth month of the study
Participants' serum androstenedione was determined.
change between the first day and the sixth month of the study
17-hydroxyprogesterone (17-OH progesterone) (ng/mL)
Time Frame: change between the first day and the sixth month of the study
Participants' serum 17-OH progesterone was determined.
change between the first day and the sixth month of the study
Sex hormone binding globulin (SHGB) (nmol/L)
Time Frame: change between the first day and the sixth month of the study
Participants' serum SHGB was determined.
change between the first day and the sixth month of the study
Free Androgen Index (FAI)
Time Frame: change between the first day and the sixth month of the study
Free Androgen Index (FAI) was calculated according to the equation FAI = [(Total testosterone/ SHBG) × 100]
change between the first day and the sixth month of the study
The Ferriman-Gallwey score (FGS)
Time Frame: change between the first day and the sixth month of the study
The Ferriman-Gallwey score (FGS) was used to evaluate hirsutism.
change between the first day and the sixth month of the study
fasting blood glucose (mg/dl)
Time Frame: change between the first day and the sixth month of the study
Participants' fasting blood gucose was calculated.
change between the first day and the sixth month of the study
fasting insulin (IU/ml)
Time Frame: change between the first day and the sixth month of the study
Participants' fasting insulin was calculated.
change between the first day and the sixth month of the study
HOMA-IR index
Time Frame: change between the first day and the sixth month of the study
Participants' HOMA-IR index value was calculated using the "fasting blood glucose (mmol/L) x fasting insulin (μU/mL)/22.5" formula
change between the first day and the sixth month of the study
QUICKI index
Time Frame: change between the first day and the sixth month of the study
Participants' QUICKI index was calculated using the 1/[log(fasting insulin in μU/ml)+log(fasting glucose in mg/dl)].
change between the first day and the sixth month of the study

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total cholesterol (mg/dl) composition
Time Frame: change between the first day and the sixth month of the study
Participants' serum total cholesterol was determined.
change between the first day and the sixth month of the study
high-density lipoprotein (HDL-C) (mg/dl)
Time Frame: change between the first day and the sixth month of the study
Participants' serum HDL-C was determined.
change between the first day and the sixth month of the study
low-density lipoprotein (LDL) (mg/dl)
Time Frame: change between the first day and the sixth month of the study
Participants' serum LDL-C was determined.
change between the first day and the sixth month of the study
triglyceride (mg/dl)
Time Frame: change between the first day and the sixth month of the study
Participants' serum triglyceride was determined.
change between the first day and the sixth month of the study
high-sensitivity CRP (HsCRP)(mg/l)
Time Frame: change between the first day and the sixth month of the study
Participants' serum HsCRP was determined.
change between the first day and the sixth month of the study
tumor necrosis factor-alpha (TNF-α) (pg/ml)
Time Frame: change between the first day and the sixth month of the study
Participants' serum TNF-α determined.
change between the first day and the sixth month of the study
interleukin-6 (IL-6) (pg/ml)
Time Frame: change between the first day and the sixth month of the study
Participants' serum IL-6 determined.
change between the first day and the sixth month of the study
Weight in kilograms
Time Frame: change between the first day and the sixth month of the study
Body weight measurement was made.
change between the first day and the sixth month of the study
Height in meters
Time Frame: change between the first day and the sixth month of the study
Height was measured
change between the first day and the sixth month of the study
BMI = body mass index (kg/m2)
Time Frame: change between the first day and the sixth month of the study
BMI = [body weight (kg)/(height [m])2]' was calculated
change between the first day and the sixth month of the study
Neck circumference in cm
Time Frame: change between the first day and the sixth month of the study
Neck circumference was measured
change between the first day and the sixth month of the study
. Waist circumference in cm
Time Frame: change between the first day and the sixth month of the study
waist circumference was measured
change between the first day and the sixth month of the study
body composition analysis
Time Frame: change between the first day and the sixth month of the study
body composition analysis (fat mass /kg), fat percentage (%), fat-free mass (kg)) were made by using the InBody 720 (1-1000 kHz; InBody Co., Ltd. Korea)
change between the first day and the sixth month of the study

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Chair: Rukiye BOZBULUT, Dr, Gazi Univeristy
  • Study Chair: Mahmut Orhun Çamurdan, prof, Gazi University
  • Study Director: Aysun Bideci, prof, Gazi University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2021

Primary Completion (Actual)

December 5, 2021

Study Completion (Actual)

February 1, 2022

Study Registration Dates

First Submitted

February 22, 2023

First Submitted That Met QC Criteria

March 3, 2023

First Posted (Actual)

March 14, 2023

Study Record Updates

Last Update Posted (Actual)

March 14, 2023

Last Update Submitted That Met QC Criteria

March 3, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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