- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05768724
Two Different Dietary Interventions for Girls With Polycystic Ovary Syndrome
Beneficial Effects of Resemena Diet on Anthropometric, Metabolic and Reproductive Profile in Adolescents With Obesity and Polycystic Ovary Syndrome: a Randomized Controlled Intervention Study
Study Overview
Status
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey, 06500
- Esra Döğer
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
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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.
|
|
Experimental: conrol group
American Heart Association (AHA) guidelines based diet was applied to adolescents with PCOS
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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.
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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]
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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
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|
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.
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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
|
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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
|
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Height in meters
Time Frame: change between the first day and the sixth month of the study
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Height was measured
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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
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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
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change between the first day and the sixth month of the study
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. Waist circumference in cm
Time Frame: change between the first day and the sixth month of the study
|
waist circumference was measured
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change between the first day and the sixth month of the study
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body composition analysis
Time Frame: change between the first day and the sixth month of the study
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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)
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change between the first day and the sixth month of the study
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Collaborators and Investigators
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
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Gazi University Medicine
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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