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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00761553
Other study ID # 0509003026
Secondary ID NIH/NIA 5R01AG02
Status Completed
Phase N/A
First received September 25, 2008
Last updated January 16, 2013
Start date October 2005
Est. completion date June 2009

Study information

Verified date January 2013
Source Purdue University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of food supplements and strength training on appetite, the amount of energy used, and body composition.


Recruitment information / eligibility

Status Completed
Enrollment 49
Est. completion date June 2009
Est. primary completion date June 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 55 Years and older
Eligibility Inclusion Criteria:

- Adults age 55 and older

- Body mass index 20 to =35 kg/m2

- Weight stable (<4kg change within the last 3 months)

- Constant habitual activity patterns (no deviation > 1x/wk of 30 min/session within last 3 months)

- Clinically normal blood and urine profiles as determined by our study physician

- Not taking medications known to influence appetite nor any anti-inflammatory steroid medications

- No hip replacements

Exclusion Criteria:

- Adults with medical conditions that might place them at risk for participating in the study or interfere with the successful completion of the study protocol will be excluded

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Dietary supplements with exercise
Resistive exercise along with consuming two dietary supplements every day during both 8 week intervention periods, for a total of 16 weeks.
Dietary Supplement:
Dietary supplement without exercise
Consuming two dietary supplements every day during both 8 week intervention periods, for a total of 16 weeks.

Locations

Country Name City State
United States Purdue University West Lafayette Indiana

Sponsors (1)

Lead Sponsor Collaborator
Purdue University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Appetite questionnaire, urine collection, strength testing, body composition, resting metabolic rate, food records, breath sample, activity assessments, dietary supplements, nightly logs, and resistive exercise. 23 weeks No
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