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Potential Impact of Polycystic Ovarian Syndrome on Protein Modifications and Accumulation

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Mayo Clinic

Status

Completed

Conditions

Obese
Overweight
Insulin Resistance
Polycystic Ovarian Syndrome (PCOS)

Treatments

Behavioral: Aerobic Exercise Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02105428
09-007006

Details and patient eligibility

About

A goal of this study is to use a novel methodology to determine whether insulin resistance in women with polycystic ovary syndrome (PCOS) is related to the accumulation of proteins with modifications. This could lead to future research to determine if these modifications interfere with their proper function. Additionally, the investigators will determine how protein quality is affected by exercise training. Aerobic exercise enhances the endogenous oxidant buffering systems which may minimize oxidative damage to proteins. The investigators propose that aerobic exercise minimizes the accrual of modified proteins by increasing the synthesis of new proteins, but also by increasing the degradation and removal of old and damaged proteins. Based on our previous studies the investigators observed that insulin affects plasma protein synthesis and aerobic exercise improves insulin sensitivity not only in muscle but also in liver. The investigators therefore propose that aerobic exercise and related increase in insulin sensitivity (and decline in insulin levels) will reduce accumulation of old and modified skeletal muscle and plasma proteins leading to improved function.

Enrollment

44 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. BMI between 25 kg/m2 and 40 kg/m2
  2. Fasting blood glucose < 126 mg/dL
  3. Diagnosed with PCOS as outlined by the Rotterdam criteria
  4. Insulin resistant as determined by a 3 hour oral glucose tolerance test

Exclusion criteria

  1. Serum creatinine ≥1.5 mg/ dL.
  2. Serum transaminase elevation ≥ 3 times the upper limit of normal range
  3. Use of systemic glucocorticoids
  4. Use of oral anticoagulation
  5. Pregnancy

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

Sedentary Control
No Intervention group
Description:
Participants will be randomized to an exercise training program or sedentary control group. The sedentary will not perform any structured physical activity or exercise. Participants will be encouraged to maintain their sedentary lifestyle and will be monitored by an accelerometer to track physical activity.
Aerobic Exercise Training
Experimental group
Description:
Participants will perform 12-weeks of aerobic exercise training
Treatment:
Behavioral: Aerobic Exercise Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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