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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01110369
Other study ID # A1002-2
Secondary ID
Status Completed
Phase N/A
First received February 12, 2010
Last updated January 30, 2012
Start date November 2009
Est. completion date July 2011

Study information

Verified date January 2012
Source Wageningen University
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Interventional

Clinical Trial Summary

The present study is designed to investigate whether timed protein supplementation will increase skeletal muscle mass in the frail elderly population.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Frail elderly individuals

- Able to understand and perform the study procedures

Exclusion Criteria:

- Type I or type II diabetes (fasted blood glucose level =7,0 mmol)

- No recent history (within 2 years) of participating in any regular resistance exercise training program (general questionnaire)

- Use of anti-coagulation medication (except of Acetyl Salicyl acid)

- Presence of coronary heart disease (ECG)

- Renal insufficiency (eGFR <60 mL/min/1.73 m2)

- Allergic or sensitive for milk proteins

Study Design

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


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Protein drink
Protein drink twice a day during 6 months.
Other:
Resistance exercise training
Resistance exercise training twice per week during 6 months.
Dietary Supplement:
Placebo drink
Placebo drink twice a day during 6 months.

Locations

Country Name City State
Netherlands Wageningen University Wageningen Gelderland

Sponsors (3)

Lead Sponsor Collaborator
Wageningen University 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 skeletal muscle mass Baseline, 3 months and 6 months No
Secondary Physical performance Baseline, 3 months and 6 months No
Secondary Blood will be collected to assess parameters related to the outcome measures Baseline, 3 months and 6 months No
Secondary Dietary intake Baseline, 3 months and 6 months No
Secondary Physical activity Baseline, 3 months and 6 months No
Secondary Cognitive performance Baseline and 6 months No
Secondary Blood pressure Baseline, 3 months and 6 months No
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