Health Condition 1: E282- Polycystic ovarian syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women aged 18 35 years Diagnosed with PCOS based on Rotterdam criteria Not currently pregnant or planning pregnancy during the study period On stable or no pharmacological treatment for PCOS Owns a smartphone and has access to WhatsApp or similar digital tools Willing to participate in a lifestyle intervention and adhere to study protocols
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in body composition parameters (Body Mass Index and body fat percentage) from baseline to 12 weeks following a personality-matched lifestyle intervention in women with Polycystic Ovary Syndrome (PCOS).Timepoint: Baseline, at 6 weeks and 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in anthropometric parameters from baseline to 12 weeks. Change in body composition parameters from baseline to 12 weeks. Change in autonomic function from baseline to 12 weeks. Change in psychological well-being from baseline to 6 weeks and 12 weeks. Adherence to the personality-matched lifestyle intervention during the 12-week study period. Feasibility and acceptability of the lifestyle intervention assessed at 12 weeks.Timepoint: Baseline, at 6 weeks and 12 weeks | — |
Countries
India
Contacts
ACS Medical College and Hospital