The effect of lifestyle on Polycystic Ovary Syndrome

Not Applicable

• Conditions: E28.2; Polycyctic ovary syndrom.; Polycystic ovarian syndrome

• Registration Number: IRCT20240207060925N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 June 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 144

Inclusion Criteria

willingness to participate in research by obtaining written consent
Women with polycystic ovary syndrome based on Rotterdam criteria
Age interval between 20 and 45 years
Higher body mass index and 24/9
Infertility due to ovulation disorder
primary infertility

Exclusion Criteria

Use of a special diet
Prohibition of physical activities
Chronic or severe or debilitating physical diseases or known mental illnesses
hyperprolactinemia, thyroid disorders, congenital hyperadrenalism or other endocrine disorders
The addiction of the individual and the spouse to drug
secondary infertility

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sexual function score in FSFI questionnaire. Timepoint: Before the study begins (zero week) and immediately after the intervention (12 weeks) and 4 weeks after the intervention ends (16 weeks). Method of measurement: FSFI questionnaire.

Secondary Outcome Measures

Name	Time	Method
Changes in weight. Timepoint: Before the study begins (zero week) and immediately after the intervention (12 weeks) and 4 weeks after the intervention ends (16 ). Method of measurement: Weight measurement instruments.;Changes in body mass index. Timepoint: Before the study begins (zero week) and immediately after the intervention (12 weeks) and 4 weeks after the intervention ends (16 ). Method of measurement: Weight and height measurement instruments.