Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
FEMALE
ID07022340

Investigating Resistance Training for Vascular Function and Quality of Life in Perimenopausal Women

Led by University of Michigan · Updated on 2025-07-11

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Women going through perimenopause, the transition period before menopause, often experience worsening blood vessel health, mood changes, sleep problems, and reduced quality of life. This trial investigates whether resistance exercise, such as lifting weights, can improve blood vessel function and these other health aspects in women aged 40 to 60 who are starting menopause. Researchers aim to understand how resistance training affects cardiovascular risk factors during this important life stage. Participants will be randomly assigned to one of two groups. One group will perform resistance training twice a week for 16 weeks, starting with lighter weights and gradually increasing intensity. Each session includes warm-up, stretching, and exercises targeting major muscle groups. The other group will receive weekly emails with general menopause information and maintain their usual lifestyle. After 16 weeks, both groups will have assessments repeated to compare effects. Throughout the study, participants will undergo tests of vascular function and endothelial function at the start and end. They will provide blood and urine samples and complete surveys about their mood, sleep quality, and menopause-specific quality of life. The study monitors adherence to exercise and evaluates changes in these measures to assess impacts of the training program. Participation lasts for 16 weeks with follow-up assessments at the University of Michigan.

CONDITIONS

Brief Title

Hemodynamics After Resistance Training

Who Can Participate

Age: 40Years - 60Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Are between 40-60 years old
  • Have had menstrual irregularities in the last 12 months
  • Do not currently complete more than two 30-min sessions of structured exercise per week and do not do any resistance training exercise
  • Are not currently pregnant
  • Are able to exercise and your doctor has not told you that you cannot
  • Can attend a morning study visit at the University of Michigan's School of Kinesiology Building
  • Are willing to avoid food 2 hours prior to the morning study visit
  • Are willing to avoid strenuous exercise, caffeine, and alcohol 8 hours prior to the morning study visit
  • Are willing to participate in an exercise training program or health education program for 16 weeks
Not Eligible

You will not qualify if you...

  • Smoke or vape nicotine or marijuana
  • Have had an oophorectomy, hysterectomy, or surgical menopause
  • Are currently taking hormone replacement therapy
  • Have taken hormone replacement therapy in the last 6 months
  • Are taking steroidal medication or medication to treat diabetes, cholesterol, or high blood pressure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessments

Duration - 1 day

Participants complete baseline vascular function and exercise testing, provide blood and urine samples, and complete surveys about sleep, mood, and menopause-specific quality of life.

1 visit (in-person)

Intervention

Duration - 16 weeks

Participants randomized to resistance training complete two strength training sessions per week for 16 weeks. Control group participants receive weekly health education emails and maintain current lifestyle habits.

Twice weekly sessions for resistance training group; weekly emails for control group

Post-Intervention Assessments

Duration - 1 day

Participants complete post-intervention vascular function and exercise testing, and the same surveys on sleep, mood, and menopause-specific quality of life as at baseline.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

University of Michigan School of Kinesiology

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

Loading map...

Research Team

M

Marnie K. McLean, M.S.

A

Abbi D. Lane, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Similar Trials

Effects of 12-week Magnesium Supplementation on Peri-menopau...

Perimenopause

Actively Recruiting

1 location

Effects of 12-week Multi-vitamin/Mineral Supplementation on ...

Perimenopause

Actively Recruiting

1 location

An Observational Virtual Trial to Investigate the Accuracy o...

Perimenopause

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here