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Clinical Trials/NCT06585865
NCT06585865RecruitingNot Applicable

Resveratrol-mediated Changes in Extracellular Vesicle microRNA Cargo as a Novel Contributor to Resistance Training-induced Skeletal Muscle Adaptations in Older Adults

Texas Tech University1 site in 1 country36 target enrollmentStarted: June 13, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
36
Locations
1
Primary Endpoint
Circulating extracellular vesicle microRNA profile

Study Overview

Brief Summary

The main goal of this study is to find out if supplementing with resveratrol improves skeletal muscle adaptations to strengthening exercise (resistance training or strength training) in adults age 60+, and to determine whether circulating vehicles of inter-organ communication (extracellular vesicles) and their cargo might help explain those responses. The investigators will also examine whether resveratrol supplementation improves blood vessel function and cognitive function (brain health) in response to strength training.

Detailed Description

After screening and providing informed consent, participants (healthy older adults, age 60+, minimally active) will be familiarized with the procedures and undergo pre-testing. After pre-testing, participants will be assigned to supplement with resveratrol or placebo (double-blinded) daily while undergoing a strength training intervention. Strength training will be performed 3x/week for two 6-week blocks, and each visit will be supervised by a member of the study team. An additional week of testing will follow each of the two 6-week blocks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Minimally active (less than 1 hour of structured exercise/week other than walking)
  • •No resistance training for the previous 6 months
  • •Not currently taking resveratrol supplements
  • •Stable medication, supplement, dietary, and physical activity regimens for the previous 3 months and no plans to change throughout the study period
  • •Body mass at least 110 lbs

Exclusion Criteria

  • •Medical complications that could increase risk during exercise (e.g., cardiovascular disease, uncontrolled hypertension, type 1 or 2 diabetes, orthopedic contraindication to exercise, kidney disease, etc.)
  • •Cannabis or nicotine use
  • •Consume more than 7 alcohol-containing beverages per week

Arms & Interventions

Resveratrol (RSV) group

Experimental

Participants will be randomized to consume resveratrol (500 mg) daily for 14 weeks (two 6-week blocks of resistance training [supervised, full-body, 3 days/week] + one testing week [3 days] following each block) after the pre-testing period. Participants will be provided with 7 days' worth of supplements at a time in pre-filled pill boxes. Pill boxes will be refilled weekly and adherence monitored.

Intervention: Resistance training (Behavioral)

Resveratrol (RSV) group

Experimental

Participants will be randomized to consume resveratrol (500 mg) daily for 14 weeks (two 6-week blocks of resistance training [supervised, full-body, 3 days/week] + one testing week [3 days] following each block) after the pre-testing period. Participants will be provided with 7 days' worth of supplements at a time in pre-filled pill boxes. Pill boxes will be refilled weekly and adherence monitored.

Intervention: Resveratrol 500 mg oral once daily. (Dietary Supplement)

Placebo

Placebo Comparator

Participants will be randomized to consume placebo capsules (cellulose, visually identical to resveratrol capsules) daily for 14 weeks (two 6-week blocks of resistance training [supervised, full-body, 3 days/week] + one testing week [3 days] following each block) after the pre-testing period. Participants will be provided with 7 days' worth of supplements at a time in pre-filled pill boxes. Pill boxes will be refilled weekly and adherence monitored.

Intervention: Resistance training (Behavioral)

Placebo

Placebo Comparator

Participants will be randomized to consume placebo capsules (cellulose, visually identical to resveratrol capsules) daily for 14 weeks (two 6-week blocks of resistance training [supervised, full-body, 3 days/week] + one testing week [3 days] following each block) after the pre-testing period. Participants will be provided with 7 days' worth of supplements at a time in pre-filled pill boxes. Pill boxes will be refilled weekly and adherence monitored.

Intervention: Placebo (Dietary Supplement)

Outcomes

Primary Outcomes

Circulating extracellular vesicle microRNA profile

Time Frame: During pre-, mid-, and post-testing (each separated by about 6 weeks)

Circulating extracellular vesicles will be isolated from plasma and their microRNA cargo will be sequenced.

Muscle torque

Time Frame: During pre-, mid-, and post-testing (each separated by about 6 weeks)

Participants will be instructed to try and straighten their leg, against resistance, as forcefully as possible and maximal torque of the quadriceps assessed using a dynamometer.

Muscle fatigability

Time Frame: During pre-, mid-, and post-testing (each separated by about 6 weeks)

Participants will perform 32 repetitions of knee extensions on a dynamometer and the change in torque from the beginning to the end will be used to indicate fatigability.

Muscle strength

Time Frame: During pre-, mid-, and post-testing (each separated by about 6 weeks)

Participants will perform submaximal testing to assess strength on key exercises included in the strength training protocol.

Appendicular skeletal muscle mass index

Time Frame: During pre-, mid-, and post-testing (each separated by about 6 weeks)

Assessed using dual-energy x-ray absorptiometry (DEXA)

Secondary Outcomes

  • Waist-to-hip ratio(During pre-, mid-, and post-testing (each separated by about 6 weeks))
  • Vascular function(During pre-, mid-, and post-testing (each separated by about 6 weeks))
  • Cognitive function(During pre-, mid-, and post-testing (each separated by about 6 weeks))
  • Grip strength(During pre-, mid-, and post-testing (each separated by about 6 weeks))
  • Lower body strength/endurance(During pre-, mid-, and post-testing (each separated by about 6 weeks))
  • Gait speed(During pre-, mid-, and post-testing (each separated by about 6 weeks))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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