Skip to main content
Clinical Trials/NCT05156918
NCT05156918CompletedNot Applicable

The Effects of High-Intensity Exercise on Biological Age

Loma Linda University1 site in 1 country35 target enrollmentStarted: November 29, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
35
Locations
1
Primary Endpoint
venipuncture procedure

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
40 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Exercise Group

Experimental

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.

Intervention: Exercise (Other)

Control Group

Active Comparator

Control group participants will make no modifications to regular diet or exercise habits for 30 days.

Intervention: Non Exercise (Other)

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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gurinder Bains

Associate Professor School of Allied Health

Loma Linda University

Study Sites (1)

Loading locations...

Similar Trials