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NCT05394935Completed

The Effects of High-intensity and Moderate-intensity Exercise on Polycystic Ovary Syndrome

The Effects of High- and Moderate-Intensity Exercise on the Cerebrovascular and Cardiometabolic Health of Women With Polycystic Ovary Syndrome

Source: ClinicalTrials.gov · Last updated 13 Feb 2025

Brief summary (registry, in English)

This study will investigate the impact of high- and moderate-intensity exercise on the cardiometabolic and brain health of women with Polycystic Ovary syndrome (PCOS). The aim is to measure and compare normal, healthy women without PCOS, to those with the condition. All participants will undergo a blood test. The investigators will then assess the participants cardiovascular fitness by means of a maximal exercise test and measure body composition through height, weight, and hip-to-waist ratio. Participants will undergo an MRI, where the investigators will assess the participants brain structure and how the brain responds to a number of tests. The investigators will also conduct some tests that will assess the participants cognition, such as IQ, memory etc. The investigators will measure the blood vessels leading to the brain and the blood flow through them to measure how much blood the brain receives when rested, using ultrasound. The investigators will use a number of tests to look at brain function, measure the responses to these tests, and compare them between the normal, healthy women and those with PCOS. This will show if women with PCOS have a similar brain function when rested and when their brains are tested to those without the condition. The investigators will use exercise as an intervention, where the aim will be to investigate whether women with PCOS respond similarly to those without the condition to both high-intensity and moderate-intensity exercise. The tests of brain function will be repeated following the exercise, and see if both normal, healthy women and those with PCOS have a similar response to the brain function tests. All tests and measures will be compared between the PCOS group, and the healthy control group to establish any potential differences or similarities as a result of the condition.

Status (registry)
Completed
Study type
Interventional
Enrollment
34 (actual)
First submitted
10 Feb 2022
Start date
1 Jan 2020
Primary completion date
25 May 2024
Lead sponsor
Cardiff Metropolitan University
NCT number
NCT05394935

What you commit to

  • Study type: Interventional
  • Participants enrolled: 34
  • From 1 Jan 2020 to the primary completion date, 25 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Congenital adrenal hyperplasia, Cushing's syndrome, thyroid disease, hyperprolactinaemia and androgen secreting tumours.
  • Known history of cardiovascular disease.

Other

  • Pregnant or breastfeeding.
  • Contraindications to MRI (fitted with ferromagnetic devices).

Who the study is looking for

  • Polycystic Ovary Syndrome as diagnosed by any recognised criteria.
  • Inactive (less than 40 mins of structured exercise per week).

Age in the registry: 16 years to 50 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cardiff Metropolitan University
Coordinator of this site? Confirm its status
CardiffUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.