Could interval training and fasting tame PCOS insulin resistance?
NCT ID NCT07708766
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study investigates whether combining high-intensity interval training (HIIT) with intermittent fasting (14-hour fast, 10-hour eating window) can reduce insulin resistance in obese women with polycystic ovary syndrome (PCOS). Participants will follow a supervised exercise program and a 1400-calorie diet during eating hours. The researchers will measure changes in body weight, waist and hip circumference, blood sugar, and insulin levels, as well as quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high-intensity interval training and intermittent fasting diet
- What this could lead to
- If effective, this combination could offer a drug-free way to manage insulin resistance and improve quality of life in women with PCOS.
- What could go wrong
- This is a small, early-stage study with 50 participants, so results may not apply to all women with PCOS. The diet and exercise regimen may be hard to maintain long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 35 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Obese women with polycystic Ovarian Syndrome (PCOS) as clinically diagnosed by the gynecologist. * Their ages will be ranged from 20 to 35 years old. * Their body mass index will be ranged from 30-40 kg/m2. * Their waist/hip ratio will be \> 0.8. * All of them should have at least two criteria of the Rotterdam diagnostic criteria of PCOS. Exclusion Criteria: * Cushing syndrome, diabetes mellitus. * Thyroid dysfunction. * Hypothalamic amenorrhea, ovarian hyperplasia. * Respiratory, renal and liver dysfunction.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hager Tharwat Mohamed
Cairo, Egypt
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