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.

Effect of Exercise adherence strategies on the Outcomes of Home-based exercise program for Polycystic Ovary Syndrome: Randomized Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/072451

Enrollment

Registered

2024-08-13

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Intervention1: PCOS exercise prescription along with exercise adherence strategy: Exercise prescription will be designed as per the FITT’s principle and will be customized as per participant’s evaluat

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
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 study.	—

Secondary

Measure	Time frame
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).	—

Measure

Time frame

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).

—

Countries

India

Contacts

Public ContactDr Shweta Bhatbolan

SDM College of Physiotherapy

chaithragoa@gmail.com7057454919

Outcome results

None listed

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