Actively Recruiting
Strength Training and Resveratrol
Led by Texas Tech University · Updated on 2025-06-29
36
Participants Needed
1
Research Sites
59 weeks
Total Duration
On this page
Sponsors
T
Texas Tech University
Lead Sponsor
N
National Strength and Conditioning Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Strength Training and Resveratrol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 60 or older
- Minimally active, with less than 1 hour of structured exercise per week apart from walking
- No resistance training in the past 6 months
- Not currently taking resveratrol supplements
- Stable medication, supplement, diet, and physical activity routines for the past 3 months with no plans to change during the study
- Body weight of at least 110 pounds
You will not qualify if you...
- Medical conditions that increase exercise risk, such as cardiovascular disease, uncontrolled high blood pressure, diabetes type 1 or 2, orthopedic issues preventing exercise, or kidney disease
- Use of cannabis or nicotine products
- Drinking more than 7 alcoholic beverages per week
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Kinesiology & Sport Management, Texas Tech University
Lubbock, Texas, United States, 79409
Actively Recruiting
Research Team
D
Danielle E Levitt, PhD
CONTACT
J
Jacob A Mota, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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