Identifying Therapeutic Targets of Accelerated Sarcopenia
NCT ID: NCT03118050
Last Updated: 2025-12-05
Study Results
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View full resultsBasic Information
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COMPLETED
NA
95 participants
INTERVENTIONAL
2017-05-28
2023-08-21
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
SINGLE
Study Groups
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RT in T2DM
Type 2 diabetes subjects will undergo 3 months of resistance exercise training. Muscle size, strength and response to a low dose amino acids will be measured before and after training. Results of this arm will be compared to those previously obtained in healthy older subjects who participated in NCT02999802 (same training protocol) after 1:1 matching for age and sex.
Resistance exercise training
Supervised resistance exercise training, 3 times a week for 3 months
BR in healthy subjects, LAA
Healthy subjects will undergo short term bed rest with standard of care physical therapy. Muscle size, strength and response to a low dose amino acids (LAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
BR in healthy subjects, HAA
Healthy subjects will undergo short term bed rest with standard of care physical therapy. Muscle size, strength and response to a high dose amino acids (HAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
BR in T2DM, LAA
Type 2 diabetes (T2DM) subjects will undergo short term bed rest with standard of care physical therapy. Muscle size, strength and response to a low dose amino acids (LAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
BR in T2DM, HAA
Type 2 diabetes (T2DM) subjects will undergo short term bed rest with standard of care physical therapy. Muscle size, strength and response to a high dose amino acids (HAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
BR in healthy subjects, PT
Healthy subjects will undergo short term bed rest with intensive physical therapy (PT). Muscle size, strength and response to a low dose amino acids (LAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
Intensive physical therapy
Intensive weight bearing PT, daily, during bed rest
BR in T2DM, PT
Type 2 diabetes (T2DM) subjects will undergo short term bed rest with intensive physical therapy (PT). Muscle size, strength and response to a low dose amino acids (LAA) will be measured before and after bed rest.
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
Intensive physical therapy
Intensive weight bearing PT, daily, during bed rest
Interventions
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Resistance exercise training
Supervised resistance exercise training, 3 times a week for 3 months
Bed rest
Bed rest for 5 days, followed by standard rehabilitation for 2 days
Intensive physical therapy
Intensive weight bearing PT, daily, during bed rest
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Score ≥26 on the 30-item Mini Mental State Examination
* Stable body weight for at least 3 months
* Non-diabetic or with Type 2 Diabetes Mellitus
Exclusion Criteria
* Insulin therapy, significant diabetic complications, or A1c\>8%
* Impairment in Activities of Daily Living
* \>2 falls/year
* weight loss \>5% in the past 6 months
* Exercise training (≥2 sessions/week) or ≥10,000 steps/day
* Significant cardiovascular, liver, renal, blood, or respiratory disease
* Active cancer or infection
* Recent (within 3 months) treatment with anabolic steroids, systemic corticosteroids or estrogen.
* Alcohol or drug abuse
60 Years
85 Years
ALL
Yes
Sponsors
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National Institute on Aging (NIA)
NIH
The University of Texas Medical Branch, Galveston
OTHER
Responsible Party
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Principal Investigators
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Elena Volpi, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
UTMB
Locations
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Sealy Center on Aging, University of Texas Medical Branch
Galveston, Texas, United States
Countries
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Provided Documents
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Document Type: Study Protocol: 15-0229 Study Protocol
Document Type: Study Protocol and Statistical Analysis Plan: 17-0064 Study Protocol
Other Identifiers
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15-0229/17-0064
Identifier Type: -
Identifier Source: org_study_id
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