To investigate the impact of exercise adherence techniques on participants in order to find out whether they stick with the given exercise and whether there is any improvement in the symptoms of polycystic ovarian syndrome by providing them with a home based exercise program.
Phase 2
- Conditions
- Health Condition 1: E282- Polycystic ovarian syndrome
- Registration Number
- CTRI/2024/08/072451
- Lead Sponsor
- Chaithra R
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Women diagnosed with PCOS by a
certified medical practitioner
2. Age of participants: 18 years to 35
years
3. Participants who are willing to give
written informed consent
Exclusion Criteria
1. Participants with any other medical
condition which contradicts them
from participating in physical
activity.
2. Participants who are pregnant
3. Participants undergoing IVF
treatment
4. Psychiatric disorder
5. Uncooperative participants
6. Participants who are not willing to
participate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Exercise adherence calendarTimepoint: Exercise adherence calendar will be given to the participants to regularly fill it (everyday for 3 months) which will be collected back at the end of the <br/ ><br>study.
- Secondary Outcome Measures
Name Time Method Blood reports - FSH, LH, Prolactin, Testosterone, TSH, Glucose fasting, Glucose post prandialTimepoint: It will be taken during the initial assessment and after 3 months (post intervention).;KARADA scanTimepoint: It will be taken during the initial assessment and after 3 months (post intervention).;Regularity of menstrual cycleTimepoint: It will be taken during the initial assessment and after 3 months (post intervention).;The Modified Ferriman-Gallwey (Mfg) ScoreTimepoint: It will be taken during the initial assessment and after 3 months (post intervention).;Waist hip ratioTimepoint: It will be taken during the initial assessment and after 3 months (post intervention).