RecruitingNot ApplicableNCT04151901

Sex-specific Determinants of Early-phase Recovery From Skeletal Muscle Disuse


Sponsor

The University of Texas Health Science Center at San Antonio

Enrollment

80 participants

Start Date

Aug 27, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This project is a 2-phase, randomized clinical trial that includes 7 days of unilateral leg disuse (Phase 1), immediately followed by 1 week of bilateral leg rehabilitation (Phase 2). The investigators will recruit cohorts of healthy middle-aged men and women to address their aims: * Demonstrate the sex-specific effects of skeletal muscle disuse (Phase 1) * Identify key molecular determinates of susceptibility of skeletal muscle atrophy (Phase 1) * Map the early, sex-specific molecular time-course of rehabilitation (Phase 2) * Determine if disused and healthy muscle respond similarly to exercise (Phase 2) Healthy, middle-age men and post-menopausal women (50-65 years) will be recruited from the greater Houston/Galveston area. This under-represented research demographic demonstrate few negative metabolic or phenotypic signs of advanced age, but are at increased risk of being hospitalized and experiencing accelerated loss of lean mass and muscle function that parallels a much older population. The goal of this study is to characterize phenotypic and molecular skeletal muscle changes in middle-aged men and women during critical periods of disuse and rehabilitation and ultimately direct the development of targeted and effective prevention and treatment strategies.


Eligibility

Min Age: 50 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study examines how the muscles of middle-aged men and postmenopausal women respond to a week of leg inactivity (achieved by having participants use crutches and avoid using one leg) followed by a week of rehabilitation exercise, with a focus on identifying biological differences between sexes that affect muscle loss and recovery. Understanding these sex-specific differences could help develop better, targeted recovery programs for people who experience muscle loss after hospitalization or injury. Healthy adults aged 50–65 — men and postmenopausal women with a BMI of 18.5–35 kg/m² and no major cardiovascular, pulmonary, or musculoskeletal conditions — may be eligible. Participation involves a two-week study protocol with supervised leg disuse followed by guided rehabilitation, muscle biopsies, and various physical and blood tests. This summary was generated by AI to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERResistance Exercise Rehabilitation

Following disuse, the REHAB groups (M-REHAB, F-REHAB) will complete monitored resistance exercise rehabilitation sessions using an isokinetic dynamometer at a similar relative load at each rehab visit.

OTHERWalking-based rehabilitation

Following disuse, the CON groups (M-CON, F-CON) will complete 30 minutes of monitored walking at a moderate intensity at each rehab visit.


Locations(2)

University of Texas Medical Branch

Galveston, Texas, United States

University of Texas Health Science Center at San Antonio

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04151901


Related Trials