- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03888040
Fatigability of Lower Limb Muscle in Older Adults: Protective Effects of Strength Training Exercise in Old Men and Women
February 8, 2025 updated by: Marquette University
Fatigability of Limb Muscle in Older Adults: Protective Effects of Exercise
The proposed studies will assess 1) the mechanisms for the age-related increase in fatigability during dynamic exercise (Aims 1 and 2) and 2) the effectiveness of high-velocity resistance training coupled with blood flow restriction (BFR) in improving muscle power output and fatigability in older adults (Aim 3).
The first two aims are cross-sectional studies comparing young (18-35 years old) and older adults (≥60 yrs old) to test our central hypothesis that the greater accumulation of metabolites and increase in fatigability in older adults is due to either age-related impairments in skeletal muscle bioenergetics (Aim 1) and/or vascular dysfunction (Aim 2).
These two aims will integrate techniques to assess whole-muscle bioenergetics (31P-MRS) and in vivo vascular function (near infrared spectroscopy; NIRS and doppler ultrasonography) with in vitro assessment of single fiber bioenergetics (epifluorescence microscopy) and vasoreactivity of isolated skeletal muscle arterioles (video microscopy).
We will then determine whether bioenergetics, vascular function and fatigability are altered in older men and women in response to 8 weeks of resistance exercise training of the lower limb both with and without blood flow restriction (Aim 3).
Study Overview
Study Type
Interventional
Enrollment (Estimated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Christopher W Sundberg, PhD
- Phone Number: 414-288-5607
- Email: christopher.sundberg@marquette.edu
Study Contact Backup
- Name: Sarah Lessila
- Email: slessila@umich.edu
Study Locations
-
-
Wisconsin
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Milwaukee, Wisconsin, United States, 53201
- Recruiting
- Marquette University
-
Contact:
- Christopher W Sundberg, PhD
- Phone Number: 414-288-5607
- Email: christopher.sundberg@marquette.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- men and women aged 18-40 years and >60 years
Exclusion Criteria:
- body mass index ≥40 kg/m2;
- type 1 or type 2 diabetes;
- uncontrolled hypertension;
- active cancer, cancer in remission, or having received treatment for any form of cancer in the previous five years;
- coronary artery disease;
- cardiovascular disease (e.g., PAD, PVD);
- abnormal and untreated thyroid function;
- chronic and/or regular nonsteroidal anti-inflammatory drugs (NSAID) consumption,
- tobacco use (includes smoking);
- any condition that presents a limitation to exercise (e.g., severe arthritis, COPD, neuromuscular disorder, moderate or severe cognitive impairment, Alzheimer's Disease, severe untreated sleep apnea).
- women who are pregnant or likely to be pregnant.
- Subjects will be excluded if they have joint pain in the exercising leg or arm. Medication use. Medications currently taken or in the previous year and known to influence muscle mass (e.g., glucocorticoids, testosterone) and cortical and neuromuscular excitability will be exclusionary, while medications that may be prevalent among older adults (e.g., statins) will be accounted for with a covariate statistical model.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Blood Flow Restriction Training
This leg will then perform low-load resistance training (30% of 1-RM) including 3 sets of 15 knee extensions performed as fast as possible while seated upright in a knee extension weight machine.
Sets will be interspersed with 30 seconds rest.
This leg will always perform the training with blood flow restriction.
|
The participant will attend 3 training sessions per week for 8 weeks.
Resistance training will be performed by each leg with a load of 30% of maximal strength: one leg with and the other without blood flow restriction.
|
|
Experimental: Resistance Training Only
This leg will then perform low-load resistance training (30% of 1-RM) including 3 sets of 15 knee extensions performed as fast as possible while seated upright in a knee extension weight machine.
Sets will be interspersed with 30 seconds rest.
This leg will always perform the training without blood flow restriction.
|
The participant will attend 3 training sessions per week for 8 weeks.
Resistance training will be performed by each leg with a load of 30% of maximal strength: one leg with and the other without blood flow restriction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Fatigability of the knee extensor muscles from baseline to after 8 weeks training
Time Frame: One session before and then after 8 weeks of training
|
Fatigability will be quantified as the change in limb muscle power output from the start ot the end of a 4-minute dynamic fatiguing exercise.
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One session before and then after 8 weeks of training
|
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Change in single muscle fiber function form baseline to after 8 weeks training
Time Frame: Before and after completion of resistance training intervention of 8 weeks.
|
Muscle Biopsies: An area of vastus lateralis will numbed by injection with local anesthetic.
A small 1/4 inch incision will be made in the skin and a needle inserted briefly into the muscle to remove a piece of muscle about the size of a pencil eraser.
The incision is pulled closed with a bandage and the area over the incision will be covered with an elastic pressure bandage.
The whole muscle biopsy procedure will take a total of approximately 15 minutes, with the actual biopsy lasting only a few seconds.
The biopsy samples will be stored for analyses and used to examine various aspects of skeletal muscle health.
|
Before and after completion of resistance training intervention of 8 weeks.
|
|
Change in muscle volume of the quadricep muscles form baseline to after 8 weeks training
Time Frame: Before and after completion of resistance training intervention of 8 weeks.
|
Magnetic resonance imaging (MRI) is used to detect the muscle volume.
|
Before and after completion of resistance training intervention of 8 weeks.
|
|
Change in muscle metabolism during a fatiguing knee extensor exercise from baseline to after 8 weeks resistance training
Time Frame: Before and 2-days after completion of resistance training intervention of 8 weeks.
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Phosphorus magnetic resonance spectroscopy (P-MRS) is used to noninvasively measure or calculate a measure of muscle metabolism using intracellular pH in the quadriceps.
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Before and 2-days after completion of resistance training intervention of 8 weeks.
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Change in vascular function via flow-mediated dilation of the femoral artery from baseline to after 8 weeks of training
Time Frame: One session before and one after 8 weeks of training
|
Macrovascular endothelial function of the leg with doppler ultrasonography by measuring the blood flow response (velocity and arterial diameter) of the femoral artery after 5 minutes of lower limb occlusion
|
One session before and one after 8 weeks of training
|
|
Change in myofibrillar-ATPase efficiency from baseline to after 8 weeks of training
Time Frame: One session before and after 8 weeks of training
|
Myofibrillar ATPase efficiency will be measured during shortening contractions in single fibers isolated from biopsies of the vastus lateralis via epifluorescence microscopy
|
One session before and after 8 weeks of training
|
|
Change in Oxygenation of the muscle between baseline to after 8 weeks of training
Time Frame: One session before and after 8 weeks of training
|
Tissue oxygenation levels of the knee extensors muscles will be measured during the 4-minute dynamic fatiguing exercise with near infrared spectroscopy
|
One session before and after 8 weeks of training
|
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Change in arteriole Vasodilation from baseline to after 8 weeks of training
Time Frame: One session before and after 8 weeks of training
|
Acetylcholine-induced vasodilation will be measured in arterioles excised from muscle biopsies of the vastus lateralis via video microscopy
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One session before and after 8 weeks of training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Strength
Time Frame: One session before and after 8 weeks of training
|
|
One session before and after 8 weeks of training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2020
Primary Completion (Estimated)
March 31, 2025
Study Completion (Estimated)
August 31, 2025
Study Registration Dates
First Submitted
March 14, 2019
First Submitted That Met QC Criteria
March 21, 2019
First Posted (Actual)
March 25, 2019
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 8, 2025
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- HR-2945
- R01AG048262 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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