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yoga and Ayurvedic diet for PCOS

Yoga along with Ayurvedic diet for the management of Polycystic Ovary Syndrome: Feasibility Randomised Comparative Study. - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073227
Enrollment
40
Registered
2024-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E282- Polycystic ovarian syndrome

Interventions

None listed

Sponsors

Vibhuti Samarth Rao
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women aged 18 to 35 years diagnosed with PCOS based on the Rotterdam Criteria in the past 1 year with a BMI of 23 to 29.9, not taking any pharmacological, nutritional, or herbal treatments for PCOS, and being able to read and understand basic English.

Exclusion criteria

Exclusion criteria: Currently pregnant, less than 6 weeks postpartum, diagnosed with severe anaemia, unwilling or unable to provide consent & adhere to the protocol, unable to travel to study sites for data collection, known cases of liver, kidney, cancer, and cardiovascular conditions, following any special diets such as time-restricted fasting, ketogenic diet, and vegan diet, known cases of gluten or lactose intolerance or any food allergy, on medication for metabolic, psychological disorders and other endocrine disorders.

Design outcomes

Primary

MeasureTime frame
Feasibility (recruitment, adherence, acceptability, adverse events, appropriateness of outcome measures and participants experiences)Timepoint: During and at the end of the trial at 12 weeks

Secondary

MeasureTime frame
Anthropometric (Waist-to-hip ratio in cm, Weight in kg, BMI, Percent body fat in %, Visceral fat area in cm2, Percent subcutaneous fat in %, Resting metabolism and Skeletal muscle mass in kg), Quantitative, qualitative assessment of dietary habits including diet-related behavioural modification, Stress level, Sleep Quality, Obesity-related quality of life, and PCOS-related quality of life. Timepoint: Before and after the trial at 0 and 12 weeks respectively

Countries

India

Contacts

Public ContactVibhuti Samarth Rao

Medical Research centre- Kasturba Health Society,

drshobhaudipi@gmail.com02226715147

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026