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Clinical Trials/NCT05156918
NCT05156918
Completed
Not Applicable

The Effects of High-Intensity Exercise on Biological Age

Loma Linda University1 site in 1 country35 target enrollmentNovember 29, 2021
ConditionsExercise

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Exercise
Sponsor
Loma Linda University
Enrollment
35
Locations
1
Primary Endpoint
venipuncture procedure
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this graduate student research study is to determine if a high-intensity exercise program can slow or reverse biological (transcriptomic) aging and shed light on the underlying transcriptomic pathways involved.

Detailed Description

24 males and 24 females will be randomly assigned to either the control group or the exercise group. Baseline measures will be obtained, including questionnaires (on stress, sleep, depression, activity level, and fitness), body composition measures, vital signs, and a blood draw. Control group participants will make no modifications to regular diet or exercise habits for 30 days. Exercise group participants will perform supervised high intensity exercise three times per week at the LLU department of physical therapy laboratory utilizing treadmills, stationary bicycles, and rowing machines. Results will be collected following conclusion of the 30-day study protocol.

Registry
clinicaltrials.gov
Start Date
November 29, 2021
End Date
June 28, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gurinder Bains

Associate Professor School of Allied Health

Loma Linda University

Eligibility Criteria

Inclusion Criteria

  • Sex: Both Males and Females
  • Age: 40-65 years old
  • Physical Fitness: Below average scores on the Self report fitness questionnaire
  • Physical Activity: Low as measured by the International Physical Activity Questionnaire

Exclusion Criteria

  • Prior (within the last 5 years) or current history of cardiovascular disease, stroke, unexplained weight loss, clinical depression, congestive heart failure, cancer, arrythmia, respiratory disease, or other serious medical conditions that would make exercise unsafe or prevent full participation in the exercise protocol.
  • Any self-reported significant increase or decrease in activity levels within the past thirty days.
  • Current use of the following medications: antibiotics, glucocorticoids, anticoagulants, narcotics, antiepileptic medications, antipsychotics, antidepressants, and hypoglycemic agents.
  • Current self-reported pregnancy

Outcomes

Primary Outcomes

venipuncture procedure

Time Frame: Change between baseline and 30 days

Participants will have 8ml of blood drawn on two separate occasions by a certified phlebotomist. The first 8 ml (1.62tsp) blood draw will occur at 8am on day 1 of the study protocol. The second 8ml (1.62tsp) blood draw will occur approximately 30 days later. The total blood draw volume will be 16ml or approximately 3.25 teaspoons. The blood draw is to test for the effects of exercise on gene expression and aging.

Secondary Outcomes

  • Perceived stress scale survey(Change between baseline and 30 days)
  • Pittsburgh Sleep Quality Index(Change between baseline and 30 days)

Study Sites (1)

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