Health Condition 1: E282- Polycystic ovarian syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Women aged 20 to 35 years diagnosed with polycystic ovary syndrome (PCOS) based on Rotterdam criteria (meeting at least two of the following: oligo/amenorrhea, clinical or biochemical hyperandrogenism, or polycystic ovarian morphology), confirmed by a qualified gynecologist. Participants should be willing to provide written informed consent and comply with the study protocol.
Exclusion criteria
Exclusion criteria: Participants currently on hormonal therapy or oral contraceptives, pregnant or planning pregnancy, or those who have taken insulin-sensitizing agents in the past 6 weeks will be excluded. Individuals with uncontrolled or clinically significant thyroid disorders, hyperprolactinemia, severe psychiatric disorders, or other major systemic illnesses will be excluded. Participants with regular engagement in structured yoga practice or high-intensity physical activity, as well as those with regular smoking or alcohol consumption, will also be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum Anti-M llerian Hormone (AMH) levels (ng/mL)Timepoint: Baseline and 12 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hormonal Outcomes 1)Serum testosterone levels (ng/dL). 2)Fasting insulin levels (pmol/L). 3)LH, FSH, estrogen, progesterone levels. 4)Prolactin and cortisol levels 5)Thyroid profile 6)Free Androgen Index (FAI) 7)Sex Hormone Binding Globulin (SHBG)Timepoint: Baseline and 12 weeks.;Metabolic Outcomes 1)Fasting blood glucose and HbA1c 2)Insulin resistance (HOMA-IR) 3)Lipid profile. 4)Liver Function Test. 5)Waist-to-hip ratio.Timepoint: Baseline and 12 weeks.;Micronutrient Parameters 1)Vitamin D levels 2)Vitamin B12 levels 3)Iron profileTimepoint: Baseline and 12 weeks.;Psychological Parameters 1)Depression, Anxiety, and Stress (DASS-21) 2)Quality of life (PCOSQOL) 3)Life satisfaction (SWLS) 4)Psychological well-being (Oxford Happiness Questionnaire)Timepoint: Baseline and 12 weeks.;Behavioral Parameters 1)Eating behavior (self-reported food diary) 2)Sleep quality (Pittsburgh Sleep Quality Index PSQI)Timepoint: Baseline and 12 weeks.;Qualitative Outcomes 1)Participant interviews 2)Observational assessments during intervention sessionsTimepoint: Baseline and 12 weeks. | — |
Countries
India
Contacts
SVYASA Deemed to be University