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Clinical Trials/NCT01110369
NCT01110369
Completed
Not Applicable

A Protein Supplementation and Exercise Strategy to Promote Muscle Protein Anabolism in Frail Elderly People

Wageningen University1 site in 1 country62 target enrollmentNovember 2009
ConditionsSarcopenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sarcopenia
Sponsor
Wageningen University
Enrollment
62
Locations
1
Primary Endpoint
Change in skeletal muscle mass
Status
Completed
Last Updated
last year

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
November 2009
End Date
July 2011
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lisette de Groot

Professor

Wageningen University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in skeletal muscle mass

Time Frame: Baseline, 3 months and 6 months

Secondary Outcomes

  • Physical performance(Baseline, 3 months and 6 months)
  • Blood will be collected to assess parameters related to the outcome measures(Baseline, 3 months and 6 months)
  • Dietary intake(Baseline, 3 months and 6 months)
  • Physical activity(Baseline, 3 months and 6 months)
  • Cognitive performance(Baseline and 6 months)
  • Blood pressure(Baseline, 3 months and 6 months)

Study Sites (1)

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