Immune Function and Muscle Adaptations to Resistance Exercise in Older Adults (TDAP2)

The loss of muscle mass and strength due to aging leads to serious health problems for older adults. Muscle health can be improved by exercise training, but some people improve their strength substantially, whereas others improve little. The reason for this variation is unknown. This study will investigate whether function of the immune system influences how well people respond to exercise. Older Veterans who participate will have their muscle size, strength, and function measured periodically for almost a year. Participants will drink a nutritional supplement or placebo daily and complete a 36 session strength training program. Participants will be vaccinated for tetanus and donate small amounts of blood and muscle tissue during the study so that immune function can be compared to muscle outcomes during training and during a long-term follow-up. The study results should increase the investigators' understanding of the negative effects of aging on muscle and will possibly lead to better strategies for muscle maintenance and rehabilitation for older adults.

Study Overview

• Status: Completed
• Conditions: Sarcopenia; Aging; Immune Function
• Intervention / Treatment: Biological: TDAP; Other: Acute Resistance Exercise; Other: Resistance Exercise Training; Other: Post-training Follow-up; Dietary supplement: Nutritional Supplement (Muscle Armor); Dietary supplement: Placebo (Kool-Aid)

Detailed Description

Objective: The study will examine the influence of immune function in older adults on improvement of muscle mass, strength, and function by resistance training. The maintenance of those benefits during long term follow-up will also be examined. This objective will be accomplished by a double-blind randomized placebo-controlled trial of a nutritional supplement (Muscle Armor) which evidence suggests can improve immune function, promote muscle growth, and counteract muscle loss. The study premise is that aging results in decreased ability of the immune system to respond to stimuli such as exercise. The study proposes that the supplement will improve muscle health by promoting a shift in immune function of older adults from a pro-inflammatory state towards a state which supports muscle growth and maintenance.

Research Plan: The study will randomize Veterans (age 60-80, N=50) to participate in the supplement or placebo groups in a three phase study. The phases of participation correspond to the three specific aims. Aim 1 will determine if 2-weeks of supplementation improves immune function. Humoral immune function will be assessed as the response to vaccination. Innate immune function will be measured as systemic and cellular responses to acute resistance exercise that the investigators' previous studies indicate are affected by aging. Aim 2 will determine if supplementation during 36 sessions of progressive high-intensity resistance training boosts improvement in muscle size (CT scan), strength, and function (gait and balance). Muscle adaptations at the cellular levels will also be measured. Aim 3 will determine if continued supplementation for 26-weeks after completion of exercise training promotes the retention of the gains in muscle size, strength, and function. Multivariable testing will then be used to compare the results between Aims 1, 2, and 3 to determine whether or not immune function is correlated with muscle adaptation to training or detraining.

Methods: Participants will undergo nine blood draws and five muscle biopsies of the vastus lateralis over the course of the study so that the effects of the supplement on immune function and cellular adaptations to training can be measured. Three of the blood draws will be used to assess the antibody response to the tetanus, pertussis, and diphtheria vaccine. Muscle and blood will be collected before and after a bout of exercise conducted before and after the 2-weeks of supplementation prior to training. Immune function will be measured using the blood based on pro- and anti-inflammatory cytokine levels, the balance between specific T-cell subpopulations, and the proliferative capacity of mononuclear cells. Immune function will be measured in muscle based on macrophage content of specific cytokines and growth factors. The investigators' previous study showed that these muscle measures strongly correlate with size and strength gain after training. Key signaling pathways including nuclear factor-k B and PI3 kinase will also be measured. The fifth biopsy will be collected post-training to measure adaptation at the cellular level based on changes in number of satellite cells and myonuclei and fiber size. Hypotheses related to these measures will be tested with 80% power to detect at least 0.8 standard deviations difference in means between the supplement and placebo groups.

Clinical Relevance: Exercise is clearly able to affect immune function. However, the proposed study will attempt to modulate immune function and determine the effects on exercise outcomes. The study will also examine detraining, an important issue for older adults, that is usually omitted from training studies. Thus, the study will potentially advance the understanding of the mechanisms of muscle gain and loss in older adults, but more importantly, the study will evaluate a nutritional intervention as a complement to exercise for supporting muscle health during aging. Targeting the immune system may be the advantage needed for an older Veteran to successfully maintain or restore the muscle mass, strength, and function that is necessary for personal independence.

• Study Type: Interventional
• Enrollment (Actual): 59
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Arkansas
    • North Little Rock, Arkansas, United States, 72114-1706
      • Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 60 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Veteran
• Age 60-80 years
• Body Mass Index of 18.5 - 29.9 kg/m2

Exclusion Criteria:

• Currently participating in any other research study involving an intervention
• Smokes tobacco products
• Tetanus or TDAP vaccine in previous two years
• Allergic to vaccination
• Seizure in past 3 months
• Guillain-Barre Syndrome in past 3 months
• Takes the medications heparin, plavix / clopidogrel, or coumadin / warfarin
• Allergic to lidocaine
• Significant problem with fainting
• Problems walking or exercising with both legs
• Participated in a weight-lifting program targeting the thighs in last 3 months
• Pains, tightness or pressure in chest during physical activity
• Metastatic cancer or undergoing chemotherapy
• Cerebral aneurysm or intracranial bleed in past year
• End-stage congestive heart failure (NYHA Stage IV)
• Unstable abdominal or thoracic aortic aneurysm (>4cm)
• Renal disease requiring dialysis
• Allergic to vaccination
• Acute retinal hemorrhage or ophthalmologic surgery in past 3 months
• Bone fractures in the pelvis, legs, or feet in the last 3 months
• Hernia that causes pain during physical activity
• Myocardial infarction or cardiac surgery in past 3 months
• Pulmonary embolism or deep venous thrombosis in past 3 months
• Proliferative diabetic retinopathy or severe nonproliferative retinopathy
• Active suicidality or suicidal ideation
• Systemic bacterial infection
• Taking aspirin in any form and unable/unwilling to discontinue at least 10 days prior to muscle biopsy
• Unwilling to halt concurrent use of amino acid or protein supplements
• Unwilling to halt new use of nutritional supplements
• Unwilling to maintain current normal diet
• Encephalopathy in past 7 days
• Active oral or genital herpes
• Current use of appetite stimulants
• Current treatment for mania or bipolar disorder or taking lithium.
• Diagnosis of a significant cognitive deficit
• Untreated severe aortic stenosis
• Uncontrolled diabetes mellitus (HbA1C>10)
• Uncontrolled hypertension or hypotension (>160/100, <100 systolic)
• Uncontrolled malignant cardiac arrhythmia
• Unstable angina
• Allergic to latex or tape
• Bleeding or clotting disorders
• Taking any non-ASA NSAID and unable or unwilling to discontinue use for 3 days prior to muscle biopsy
• Taking Fish Oil, Gingko, Garlic, Saw Palmetto, Turmeric, or Vitamin E and unable or unwilling to discontinue use for 10 days prior to the muscle biopsy procedure
• Significant problems with chronic pain
• Uncontrolled asthma or allergies
• Taking lactulose, nitrates plus hypertension medications or Viagra
• Liver cirrhosis or other severe liver disease
• History of peripheral artery disease
• Certain Steroid or androgen use in past 3 months
• Other physician judgment
• Significantly abnormal complete blood count (CBC) or prothrombin time (PT)/partial thromboplastin time (PTT)/international normalized ratio (INR)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Nutritional Supplement; Subjects in the supplement group will consume orange-flavored Muscle Armor according to the manufacturer's directions: one serving (approximately 30g, i.e. one scoop provided with the product by its manufacturer), twice daily mixed with 12 ounces (oz) of water beginning after all baseline assessments are performed including assessment of the response to acute exercise and continuing until the end of study participation.	Biological: TDAP; Both arms will receive the tetanus, diptheria, and pertussis vaccination after two weeks of treatment with supplement or placebo; Other Names: tetanus, diptheria, and pertussis vaccination; Other: Acute Resistance Exercise; Both arms will receive a single bout of resistance exercise twice, before and after two weeks of treatment with supplement or placebo, and be evaluated for the response within blood and muscle; Other Names: Single bout of exercise; Other: Resistance Exercise Training; Both arms will receive 36 sessions of progressive high-intensity resistance exercise training (thigh muscle) over the course of approximately 12 weeks.; Other Names: Chronic exercise; Other: Post-training Follow-up; Both arms will continue to receive treatment with supplement or placebo for approximately 26 weeks after completion of the exercise training. During this time subjects will not be allowed to perform resistance exercise.; Other Names: Detraining Period; Dietary supplement: Nutritional Supplement (Muscle Armor); Subjects in the supplement group will consume orange-flavored Muscle Armor according to the manufacturer's directions: one serving (approximately 30g, i.e. one scoop provided with the product by its manufacturer), twice daily mixed with 12 ounces (oz) of water beginning after all baseline assessments are performed including assessment of the response to acute exercise and continuing until the end of study participation.
Placebo Comparator: Placebo; Subjects in the placebo group will consume orange-flavored Kool-Aid (Kraft Foods) according to the manufacturer's directions: one serving (approximately 13g, i.e. one scoop provided with the product by the pharmacy), twice daily mixed with 12 ounces (oz) of water beginning after all baseline assessments are performed including assessment of the response to acute exercise and continuing until the end of study participation.	Biological: TDAP; Both arms will receive the tetanus, diptheria, and pertussis vaccination after two weeks of treatment with supplement or placebo; Other Names: tetanus, diptheria, and pertussis vaccination; Other: Acute Resistance Exercise; Both arms will receive a single bout of resistance exercise twice, before and after two weeks of treatment with supplement or placebo, and be evaluated for the response within blood and muscle; Other Names: Single bout of exercise; Other: Resistance Exercise Training; Both arms will receive 36 sessions of progressive high-intensity resistance exercise training (thigh muscle) over the course of approximately 12 weeks.; Other Names: Chronic exercise; Other: Post-training Follow-up; Both arms will continue to receive treatment with supplement or placebo for approximately 26 weeks after completion of the exercise training. During this time subjects will not be allowed to perform resistance exercise.; Other Names: Detraining Period; Dietary supplement: Placebo (Kool-Aid); Subjects in the placebo group will consume orange-flavored Kool-Aid (Kraft Foods) according to the manufacturer's directions: one serving (approximately 13g, i.e. one scoop provided with the product by the pharmacy), twice daily mixed with 12 ounces (oz) of water beginning after all baseline assessments are performed including assessment of the response to acute exercise and continuing until the end of study participation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Plasma Concentration of Antibodies to Pertussis Antigen (1 Week Post-vaccine)	The change in plasma antibody concentration for response to the pertussis antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and one week post-vaccination.	change from baseline at 1 week post-vaccine
Change in Plasma Concentration of Antibodies to Pertussis Antigen (2 Weeks Post-vaccine)	The change in plasma antibody concentration for response to the pertussis antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and two weeks post-vaccination.	change from baseline at 2 weeks post-vaccine
Change in Plasma Concentration of C-Reactive Protein	Plasma c-reactive protein will be measured before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in the Number of Muscle Macrophages Per Myofiber (Pre- to Post-acute Exercise)	The change in the number of muscle macrophages per myofiber will be calculated for muscle collected before and 72 hours after a single bout of resistance exercise. The changes in macrophage numbers before and after two weeks of treatment with supplement or placebo will be compared.	change from baseline at 2 weeks of treatment
Change in Muscle Strength After Exercise Training for 12 Weeks	The change in muscle strength after exercise training will be measured as the difference in one-repetition maximum capability for knee extension from before and after completion of the exercise training program.	change from baseline at completion of exercise training phase (12 weeks)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Plasma Concentration of Antibodies to Tetanus Antigen (1 Week Post-vaccine)	The change in plasma antibody concentration for response to the tetanus antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and one week post-vaccination.	change from baseline at 1 week post-vaccine
Change in Plasma Concentration of Antibodies to Tetanus Antigen (2 Weeks Post-vaccine)	The change in plasma antibody concentration for response to the tetanus antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and two weeks post-vaccination.	change from baseline at 2 weeks post-vaccine
Change in Plasma Concentration of Antibodies to Diptheria Antigen (1 Week Post-vaccine)	The change in plasma antibody concentration for response to the diptheria antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and one week post-vaccination.	change from baseline at 1 week post-vaccine
Change in Plasma Concentration of Antibodies to Diptheria Antigen (2 Weeks Post-vaccine)	The change in plasma antibody concentration for response to the diptheria antigen within the tetanus, diphtheria, and pertussis (TDAP) vaccination will be measured between baseline and two weeks post-vaccination.	change from baseline at 2 weeks post-vaccine
Number of Muscle Macrophages Per Myofiber (Resting)	The number of muscle macrophages per myofiber will be counted for resting muscle collected before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in Muscle Size After Exercise Training for 12 Weeks	The change in size of the thigh muscle group after exercise training will be measured as the difference in cross-sectional area based on CT scan before and after completion of the exercise training program.	change from baseline at completion of exercise training phase (12 weeks)
Change in Muscle Strength at Week 16 of the Post-Training Period	The change in muscle strength (one-repetition maximum for knee extension) after completion of the exercise training program will be measured during a follow-up period lacking exercise.	difference between baseline and time point one of de-training follow-up period (week 16)
Change in Balance After Exercise Training for 12 Weeks	The change in balance ability after exercise training will be measured as the difference in Berg Balance Scale (Min 0, Max 56, Higher is Better) score between before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)
Change in Balance During the Post-Training Period at 26 Weeks of the Post-training Period	The change in balance based on the Berg Balance Scale (Min 0, Max 56, Higher is Better) score will be measured during a follow-up period lacking exercise after completion of the exercise training program.	difference between time of training completion and time point two of de-training follow-up period (26 weeks)
Change in Balance at Week 16 of the Post-Training Period	The change in balance based on the Berg Balance Scale (Min 0, Max 56, Higher is Better) score will be measured during a follow-up period lacking exercise after completion of the exercise training program.	difference between time of training completion and time point one of de-training follow-up period (week 16)
Change in Walking Ability After Exercise Training for 12 Weeks	The change in walking ability after exercise training will be measured using the six minute walk test, i.e. the distance the participant can walk without shortness of breath in six minutes.	change from baseline at completion of exercise training (12 weeks)
Change in Walking Ability at Week 16 of the Post-Training Period	The change in walking ability based on the six-minute walk test will be measured during a follow-up period lacking exercise after completion of the exercise training program.	difference between end of training and time point one of de-training follow-up period (week 16)
Change in Walking Ability at Week 26 of the Post-Training Period	The change in walking ability based on the six-minute walk test will be measured during a follow-up period lacking exercise after completion of the exercise training program.	difference between end of training and time point two of de-training follow-up period (week 26)
Change in Gait Speed After Exercise Training for 12 Weeks	The change in gait speed ability after exercise training will be measured as the difference in habitual walking speed for 10 meters before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)
Change in Gait Speed at Week 16 of the Post-Training Period	The change in habitual walking speed over 10 meters will be measured as the difference between values at the end of the training program and time points during a follow-up period lacking exercise.	difference between after training and time point one of de-training follow-up period (week 16)
Change in Gait Speed During at Week 26 of the Post-Training Period	The change in habitual walking speed over 10 meters will be measured as the difference between values at the end of the training program and time points during a follow-up period lacking exercise.	difference between after training and time point two of de-training follow-up period (week 26)
Change in Muscle Size at Week 26 of the Post-Training Period	The change in size of the thigh muscle group during the post-training period will be measured as the difference in cross-sectional area based on CT scan at the end of the training program and at the end of study participation.	difference between baseline and time point two of de-training follow-up period (week 26)
Change in Timed Up and Go After Exercise Training for 12 Weeks	The change in time required to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down will be measured as the difference between before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)
Change in Timed Up and Go at Week 16 of the Post-Training Period	The change in time required to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down will be measured as the difference between time points at the end of the training program and during the post-training period.	difference between after training and time point one of de-training follow-up period (week 16)
Change in Timed Up and Go at Week 26 of the Post-Training Period	The change in time required to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down will be measured as the difference between time points at the end of the training program and during the post-training period.	difference between after training and time point two of de-training follow-up period (week 26)
Percent Change in Resting Muscle Concentration of Interleukin-1 Beta	The muscle concentration of interleukin-1 beta will be measured before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in Muscle Concentration of Interleukin-1 Beta (Pre- to Post-acute Exercise)	The change in the muscle concentration of interleukin-1 beta before and one hour after a single bout of resistance exercise. The changes in macrophage numbers before and after two weeks of treatment with supplement or placebo will be compared.	change from baseline at 2 weeks of treatment
Change in Resting Muscle Atrophy Gene MURF Expression	The change in resting muscle atrophy gene MURF expression will be measured before and after two weeks of treatment with supplement or placebo.	percent change from baseline at 2 weeks of treatment
Change in Resting Muscle Atrophy Gene MURF Expression (Post-acute Exercise)	The change in resting muscle atrophy gene MURF expression will be measured before and 72 hours after a single bout of exercise completed before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in Resting Muscle Protein Kinase B	The change in resting muscle Protein Kinase B will be measured before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in Muscle Protein Kinase B (Post-acute Exercise)	The change in muscle Protein Kinase B will be measured before and 72 hours after a single bout of exercise completed before and after two weeks of treatment with supplement or placebo.	change from baseline at 2 weeks of treatment
Change in Number of Muscle Satellite Cells After Exercise Training for 12 Weeks	The change in the satellite cell content of muscle will be measured as the difference in the number of satellite cells in muscle before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)
Change in Number of Myonuclei After Exercise Training for 12 Weeks	The change in the myonuclear content of muscle will be measured as the difference in the number of myonuclei in muscle before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)
Change in Muscle Fiber Size After Exercise Training for 12 Weeks	The change in the muscle fiber size will be measured as the difference in fiber size before and after completion of the exercise training program.	change from baseline at completion of exercise training (12 weeks)

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Plasma Concentration of Aspartate Aminotransferase After Product Consumption for 15 Weeks	Plasma aspartate aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	at completion of the exercise training program (15 weeks)
Plasma Concentration of Alanine Aminotransferase After Product Consumption for 15 Weeks	Plasma Alanine Aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	completion of the exercise training program (15 weeks)
Ratio of Plasma Concentrations of Blood Urea Nitrogen to Creatinine After Product Consumption for 15 Weeks	Plasma blood urea nitrogen and creatinine will be measured as a safety indicator of kidney function at baseline, after completion of the exercise training program, and at the end of the study.	completion of the exercise training program (15 weeks)
Plasma Concentration of Aspartate Aminotransferase After 42 Weeks of Product Consumption	Plasma aspartate aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	end of study (42 weeks)
Plasma Concentration of Alanine Aminotransferase After 42 Weeks of Product Consumption	Plasma Alanine Aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	end of study (42 weeks)
Ratio of Plasma Concentrations of Blood Urea Nitrogen to Creatinine After 42 Weeks of Product Consumption	Plasma blood urea nitrogen and creatinine will be measured as a safety indicator of kidney function at baseline, after completion of the exercise training program, and at the end of the study.	end of study (42 weeks)
Change in Muscle Strength at Week 26 of the Post-Training Period	The change in muscle strength (one-repetition maximum for knee extension) after completion of the exercise training program will be measured during a follow-up period lacking exercise.	difference between baseline and time point two of de-training follow-up period (week 26)
Plasma Concentration of Aspartate Aminotransferase	Plasma aspartate aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	baseline
Plasma Concentration of Alanine Aminotransferase	Plasma Alanine Aminotransferase will be measured as a safety indicator of liver function at baseline, after completion of the exercise training program, and at the end of the study.	baseline
Ratio of Plasma Concentrations of Blood Urea Nitrogen to Creatinine	Plasma blood urea nitrogen and creatinine will be measured as a safety indicator of kidney function at baseline, after completion of the exercise training program, and at the end of the study.	baseline

Collaborators and Investigators

• Sponsor: VA Office of Research and Development
• Collaborators: University of Arkansas
• Investigators: Principal Investigator: Richard A Dennis, PhD, Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR

Publications and helpful links

General Publications

• Long DE, Villasante Tezanos AG, Wise JN, Kern PA, Bamman MM, Peterson CA, Dennis RA. A guide for using NIH Image J for single slice cross-sectional area and composition analysis of the thigh from computed tomography. PLoS One. 2019 Feb 7;14(2):e0211629. doi: 10.1371/journal.pone.0211629. eCollection 2019.
• Dennis RA, Long DE, Landes RD, Padala KP, Padala PR, Garner KK, Wise JN, Peterson CA, Sullivan DH. Tutorial for using SliceOmatic to calculate thigh area and composition from computed tomography images from older adults. PLoS One. 2018 Oct 2;13(10):e0204529. doi: 10.1371/journal.pone.0204529. eCollection 2018.
• Kosmac K, Peck BD, Walton RG, Mula J, Kern PA, Bamman MM, Dennis RA, Jacobs CA, Lattermann C, Johnson DL, Peterson CA. Immunohistochemical Identification of Human Skeletal Muscle Macrophages. Bio Protoc. 2018 Jun 20;8(12):e2883. doi: 10.21769/BioProtoc.2883.
• Dennis RA, Ponnappan U, Kodell RL, Garner KK, Parkes CM, Bopp MM, Padala KP, Peterson CA, Padala PR, Sullivan DH. Immune Function and Muscle Adaptations to Resistance exercise in Older Adults: Study Protocol for a Randomized Controlled Trial of a Nutritional Supplement. Trials. 2015 Mar 27;16:121. doi: 10.1186/s13063-015-0631-3.

Study record dates

Study Major Dates

• Study Start (Actual): July 23, 2014
• Primary Completion (Actual): December 31, 2018
• Study Completion (Actual): September 30, 2019

Study Registration Dates

• First Submitted: September 19, 2014
• First Submitted That Met QC Criteria: October 6, 2014
• First Posted (Estimate): October 10, 2014

Study Record Updates

• Last Update Posted (Actual): September 28, 2021
• Last Update Submitted That Met QC Criteria: August 31, 2021
• Last Verified: August 1, 2021

More Information

Terms related to this study

• Keywords: resistance exercise; exercise training; interleukin-1; Juven; insulin-like growth factor
• Additional Relevant MeSH Terms: Nervous System Diseases; Neurologic Manifestations; Neuromuscular Manifestations; Pathological Conditions, Anatomical; Muscular Atrophy; Atrophy; Sarcopenia
• Other Study ID Numbers: E1203-R; RX001203 (Other Grant/Funding Number: VA Rehabilitation R&D Application); 608119 (Other Identifier: CAVHS Institutional Review Board)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No