Polycyctic ovary syndrom. Polycystic ovarian syndrome
Conditions
Interventions
Intervention 1: Intervention group:The intervention group is given a lifestyle modification program for12 weeks that includes recommendations for healthy eating, including the elimination of simple ca
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMina Iravani
Ahvaz University of Medical Sciences
Outcome results
None listed