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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01004588
Other study ID # MEC 09-3-056
Secondary ID
Status Completed
Phase N/A
First received October 26, 2009
Last updated April 9, 2015
Start date November 2009
Est. completion date November 2012

Study information

Verified date April 2015
Source Maastricht University Medical Center
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

The main objective of this study is to examine the effects of resistance type exercise training combined with nutritional support on body composition and muscle characteristics in healthy elderly men and women. For a comprehensive insight into the potential underlying mechanisms of the intervention effects on whole body-, muscle- and myocellular level, a broad range of tests will be performed before, during, and after the intervention period.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date November 2012
Est. primary completion date November 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years to 90 Years
Eligibility Inclusion Criteria:

- over 65 years

- healthy men and women

Exclusion Criteria:

- cardiovascular disease

- COPD

- Parkinson

- rheumatoid arthritis

- musculoskeletal/orthopaedic disorders

- cognitive impairment

- subjects with metal implants

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Protein drink
total of 15 g protein/d in a protein drink consumed every morning after breakfast during 24 weeks
placebo drink
subjects consume a placebo drink every morning after breakfast over a period of 24 weeks.

Locations

Country Name City State
Netherlands Maastricht University Maastricht

Sponsors (2)

Lead Sponsor Collaborator
Maastricht University Medical Center Top Institute Food and Nutrition

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in muscle mass measured by DXA-scan and CT-scan 0, 12 and 24 weeks No