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

Cardiff Metropolitan University

Status: Enrolling

Conditions: Polycystic Ovary Syndrome; Cerebrovascular Circulation; Exercise

Treatments: Other: High-Intensity Exercise; Other: Moderate-Intensity Exercise

Study type: Interventional

Funder types: Other

Identifiers

NCT05394935

STA-1653

Details and patient eligibility

About

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.

Enrollment: 40 estimated patients

Sex: Female

Ages: 16 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• Pregnant or breastfeeding.
• Congenital adrenal hyperplasia, Cushing's syndrome, thyroid disease, hyperprolactinaemia and androgen secreting tumours.
• Known history of cardiovascular disease.
• Contraindications to MRI (fitted with ferromagnetic devices).

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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40 participants in 2 patient groups

Polycystic Ovary Syndrome

Experimental group

Description:

Women with PCOS

Treatment:

Other: High-Intensity Exercise

Other: Moderate-Intensity Exercise

Controls

Active Comparator group

Description:

Healthy, age and BMI matched controls

Treatment:

Other: High-Intensity Exercise

Other: Moderate-Intensity Exercise