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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00872911
Other study ID # 08-085
Secondary ID 5R01AG030070
Status Completed
Phase Phase 1
First received March 27, 2009
Last updated December 8, 2016
Start date March 2009
Est. completion date August 2016

Study information

Verified date December 2016
Source The University of Texas Medical Branch, Galveston
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The investigators' general hypothesis is that nutritional factors, including protein/energy malnutrition and/or an impaired response of muscle to nutrition, and inactivity play significant roles in developing sarcopenia, the involuntary loss of muscle mass and function with age. Therefore, age-specific prolonged interventions including nutritional manipulations and/or exercise may help to reduce, stabilize, or even reverse sarcopenia.


Description:

Our preliminary studies indicate that, in older adults, muscle protein anabolism is normally stimulated by amino acids alone, but impaired when nutritional stimuli contain carbohydrate due to a relative insulin resistance of muscle protein synthesis. We have also found that amino acids are the most efficient nutrients for the acute stimulation of muscle protein anabolism and our pilot data suggest that they can also increase muscle mass in healthy older adults.

Inactivity is another likely contributor to sarcopenia. Exercise increases not only muscle protein synthesis,mass and strength, but also energy expenditure. Hence, exercise may improve the response of muscle to nutritional interventions in older subjects via increased energy requirements and food consumption, thereby allowing for achievement of true supplementation.

We will test the following specific hypotheses in older, community indwelling, sedentary subjects:

Using a factorial design we will address in older, community-indwelling, sedentary subjects the following hypotheses:

1. Nutritional supplementation with amino acids will improve muscle mass, strength, function, quality, and protein synthesis.

2. Progressive exercise training for 24 weeks will improve muscle mass strength,function, quality, perfusion, and protein metabolism.

3. Combined treatment with nutritional supplementation and progressive exercise training for 24 weeks will improve muscle mass, strength, function, quality, perfusion, and protein metabolism more than either intervention alone.

Our goal is to establish if specific interventions that can acutely increase muscle protein synthesis can also effectively translate into increased muscle mass and/or performance in older sedentary people, thus preventing frailty and promoting physical independence. To this end we will use stable isotope methodologies to measure muscle protein metabolism and contrast enhanced ultrasound to measure muscle perfusion, in order to determine if the treatments' acute effects can predict their chronic impact on muscle mass and function. We will also determine if chronic treatment leads to metabolic and/or vascular adaptations that may explain the measured changes in muscle mass and function.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date August 2016
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria:

1. age 65-85 yrs

2. ability to sign consent form (score >25 on the 30 item Mini Mental State Examination, MMSE)

3. stable body weight for at least 1 year (verified via medical records).

Exclusion Criteria:

1. physical dependence or frailty (impairment in any of the Activities of Daily Living (ADL), history of falls (=2/year) or significant weight loss in the past year)

2. exercise training (=2 weekly sessions of moderate-to-high intensity aerobic or resistance exercise)

3. significant heart, liver, kidney, blood or respiratory disease

4. peripheral vascular disease

5. diabetes or other untreated endocrine disease

6. active cancer

7. recent (within 6 months) treatment with anabolic steroids, or corticosteroids

8. alcohol or drug abuse

9. tobacco use (smoking or chewing, verified via medical records)

10. depression (>5 on the 15-item Geriatric Depression Scale (GDS))

11. malnutrition (BMI <20 kg/m2; hypoalbuminemia or hypotransferrenemia; protein intake<0.66 g/kg/day at run-in)

12. obesity (BMI>30 kg/m2).

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Amino acids
mixed pure crystalline amino acids for human use (Ajinomoto), 15 g/d
Drug:
Exercise
progressive exercise training

Locations

Country Name City State
United States Sealy Center on Aging, University of Texas Medical Branch Galveston Texas

Sponsors (2)

Lead Sponsor Collaborator
The University of Texas Medical Branch, Galveston National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle mass 6 months No
Secondary Muscle function 6 months No
Secondary muscle protein turnover 6 months No
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