Adults 20 to 40, female only, with Polycystic Ovary Syndrome. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Serum TestosteronePrimary· 0 weeks to 12-weeks
Levels of serum testosterone
0-week
Group
Value
95% CI
HIIT Group
2.54
± 0.07
ST Group
2.54
± 0.09
12-weeks
Group
Value
95% CI
HIIT Group
2.39
± 0.14
ST Group
2.47
± 0.09
Body Fat PercentagePrimary· 0-week to 12-weeks
Using skinfold method (body caliper)
0-week
Group
Value
95% CI
HIIT Group
31.59
± 1.79
ST Group
34.12
± 2.69
12-weeks
Group
Value
95% CI
HIIT Group
29.62
± 1.76
ST Group
32.48
± 2.87
Physical ActivityPrimary· 0-week to 12-weeks
International physical activity questionnaire
0-week
Group
Value
95% CI
HIIT Group
3491.15
± 211.99
ST Group
3439.60
± 243.76
12-weeks
Group
Value
95% CI
HIIT Group
3928.10
± 220.04
ST Group
3716.60
± 234.45
Sponsor's own description
This RCT is aimed towards determining the effectiveness of exercises based intervention strategy involving high intensity interval training exercises in improving serum testosterone level, body fat composition and physical activity in hopes to provide a definitive exercise regime for the ever common symptoms of pcos. It will be based on the theory that exercise helps in decreasing testosterone level that in turn decrease high androgen levels in the body, exercise further decreases body fat composition (obesity is a common cause or manifestation of pcos).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Ziauddin University
Last refreshed: 2 February 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04942366.