RECRUITING

Short-term Circuit Training on Muscle Mass and Quality of Life in Sedentary Postmenopausal Women

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Postmenopausalbalance

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this graduate student research study is to provide healthcare professionals with evidence of the potential of circuit strength training in improving the physical and psychosocial well-being of postmenopausal women.

Official Title

The Effects of Short-Term Circuit Strength Training Intervention on Muscle Mass, Metabolic Health, Balance, Quality of Life, and Inflammaging in Sedentary Postmenopausal Women

Quick Facts

Study Start:2024-05-29
Study Completion:2025-05-29
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06445842

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:50 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Females aged between 50 and 75 years.
  2. * Self-reported postmenopausal status (i.e., cessation of menstruation for a minimum of 12 months).
  3. * Physically capable of participating in an exercise intervention.
  4. * No engagement in structured resistance or aerobic training programs in the six months preceding the study.
  1. * Classification as moderate and highly active on the International Physical Activity Questionnaire (IPAQ) (600-3000 MET-minutes/week for "moderate" and higher than 3000 MET-minutes/week for "high" score)
  2. * Diagnosis of any health condition that constitutes a contraindication to physical exercise (e.g., significant cardiovascular disease, orthopedic or neuromuscular restrictions impacting exercise performance or safety).
  3. * Regular use of medication with the potential to affect study outcomes (e.g., corticosteroids, immunosuppressants).

Contacts and Locations

Study Contact

Everett Lohman, Dsc
CONTACT
(909) 558-1000
elohman@llu.edu

Principal Investigator

Everett Lohman, DSc
PRINCIPAL_INVESTIGATOR
Loma Linda University

Study Locations (Sites)

Loma Linda University
Loma Linda, California, 92354
United States

Collaborators and Investigators

Sponsor: Loma Linda University

  • Everett Lohman, DSc, PRINCIPAL_INVESTIGATOR, Loma Linda University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-29
Study Completion Date2025-05-29

Study Record Updates

Study Start Date2024-05-29
Study Completion Date2025-05-29

Terms related to this study

Keywords Provided by Researchers

  • postmenopausal
  • balance

Additional Relevant MeSH Terms

  • Postmenopausal