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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00635739
Other study ID # 1493
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2008
Est. completion date May 2011

Study information

Verified date December 2018
Source Tufts University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research study is looking at the effects of a whey protein nutritional supplement on changes in muscle mass, strength and physical function in response to a 6 month program of strength training exercise.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date May 2011
Est. primary completion date May 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 70 Years to 85 Years
Eligibility Inclusion Criteria:

- Male and Females 70-85 yrs

- Community dwelling

- Short Physical Performance Battery score < 10

- BMI = 21-32.5

Exclusion Criteria:

- Acute or terminal illness

- Mini Mental State Exam < 23

- Myocardial infarction in previous 6 months, symptomatic coronary artery disease, or congestive heart failure

- Upper or lower extremity fracture in previous 6 months

- Uncontrolled hypertension (>150/90 mm Hg).

- Neuromuscular diseases and drugs which affect neuromuscular function.

- Hormone replacement therapy

- eGFR <30 mL/min/1.73m2

- Types I and II Diabetes Mellitus

- Dietary protein intake < 0.8 g.kg-1.day-1

- Disorders of nutrient absorption

- Milk, or whey allergy

- Sulfa drugs and allergy to PABA-containing sunscreens

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Whey protein
powdered, 46g supplement dissolved in fluids, twice daily
Maltodextrin placebo
powdered, 46g supplement dissolved in fluids, twice daily

Locations

Country Name City State
United States Jean Mayer USDA Human Nutrition Research Center on Aging Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Tufts University National Dairy Council

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 1 Repetition Maximum Muscle Strength 1-RM (N) Double Leg Press The maximum muscle strength of the leg extensor muscles as measured by pneumatic strength training equipment. Baseline and follow up (6 months)
Secondary Lean Mass Whole body lean mass (kg) as measured by dual energy x-ray absorptiometry. Baseline and follow up (6 months)
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