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Improving Reproductive Function in Women With Polycystic Ovary Syndrome by High Intensity Interval Training (IMPROV-IT)

N

Norwegian University of Science and Technology

Status

Completed

Conditions

Polycystic Ovary Syndrome

Treatments

Behavioral: 10x1 minute high intensity interval training
Behavioral: 4x4 minutes high intensity interval training

Study type

Interventional

Funder types

Other

Identifiers

NCT02419482
2015/468

Details and patient eligibility

About

The aim is to investigate whether 16 weeks of high intensity interval training, followed by 36 weeks of home-based exercise, will improve menstrual frequency in women with Polycystic Ovary Syndrome (PCOS) compared with a non-exercising control group.

Enrollment

64 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Polycystic ovary syndrome (PCOS) according to the Rotterdam criteria

Exclusion criteria

  • Regular high intensity endurance (two or more times per week of vigorous exercise).
  • Concurrent treatments (insulin sensitizers or drugs known to affect gonadotropin or ovulation, with a wash out period of 1 months prior to inclusion).
  • On-going pregnancy.
  • Breast feeding within 24 weeks
  • Cardiovascular disease or endocrine disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

64 participants in 3 patient groups

4x4 minutes interval training
Experimental group
Description:
4x4 minutes high intensity interval training with 4 minute intervals
Treatment:
Behavioral: 4x4 minutes high intensity interval training
10x1 minute interval training
Experimental group
Description:
10x1 minute high intensity interval training with 1 minute intervals
Treatment:
Behavioral: 10x1 minute high intensity interval training
control
No Intervention group
Description:
Physical activity recommended

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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