Comparing high intensity circuit training and intermittent fasting for women with PCOS
Effects of High Intensity Circuit Training and Intermittent Fasting on Polycystic Ovarian Syndrome
This study is testing whether high intensity circuit training, intermittent fasting, or a mix of both can help women with PCOS manage their symptoms better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 33 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | Riphah International University Academic / other |
| Locations | 2 sites (Rawalpindi, Punjab Province and 1 other locations) |
| Trial ID | NCT06302166 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial aims to evaluate the effects of High Intensity Circuit Training (HICT), Intermittent Fasting (IF), and their combination on various aspects of Polycystic Ovary Syndrome (PCOS) in females. Participants will be divided into three groups, each receiving one of the interventions, and outcomes will include PCOS morphology, anthropometric measurements, clinical hyperandrogenism, and body image concerns. The study seeks to determine which approach, or combination thereof, is most effective in managing symptoms associated with PCOS.
Who should consider this trial
Good fit: Ideal candidates for this study are unmarried females diagnosed with PCOS Phenotype A who have not engaged in regular lifestyle interventions for at least three months.
Not a fit: Patients with a BMI of 27 or higher, those on hormonal medications, or those with diabetes or thyroid disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective lifestyle interventions for managing PCOS symptoms and improving quality of life for affected women.
How similar studies have performed: While there is ongoing research into lifestyle interventions for PCOS, the specific combination of HICT and IF in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Unmarried females * Diagnosed with PCOS Phenotype A based on Rotterdam Criteria: * PCOM on US * Ovulatory dysfunction * Clinical Hyperandrogenism (Hirsutism modified Ferriman Gallway score ≥ 8) * Not engaged in any regular lifestyle intervention for \<3 Months prior to inclusion Exclusion Criteria: * Use of Estrogen, Progestin or combination. * Taking medications or supplements for Insulin resistance \< 3 months prior to the inclusion * Type I or II DM * Hypo/hyperthyroidism * BMI ≥27 (Obese according to BMI Asia)
Where this trial is running
Rawalpindi, Punjab Province and 1 other locations
- Bilal Hospital — Rawalpindi, Punjab Province, Pakistan (Recruiting)
- Noor Clinic — Rawalpindi, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Sarah Ehsan, PP-DPT — Riphah International University
- Study coordinator: Imran Amjad, PhD
- Email: imran.amjad@riphah.edu.pk
- Phone: 033324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.