Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Resistance Training in Elderly
This study has been completed.
Sponsors and Collaborators: Maastricht University Medical Center
The Anna Foundation
DSM Food Specialties
Information provided by: Maastricht University Medical Center
ClinicalTrials.gov Identifier: NCT00744094
  Purpose

In the present study the investigators aim to determine whether protein supplementation can augment the response to a 12 week resistance training program in healthy elderly men.


Condition Intervention Phase
Sarcopenia
Atrophy
Aging
Dietary Supplement: protein drink
Behavioral: Resistance training
Phase I
Phase II

U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: The Influence of Resistance Training on Body Composition and Muscle Characteristics in Healthy Elderly

Further study details as provided by Maastricht University Medical Center:

Primary Outcome Measures:
  • Muscle mass measured at limb and cellular level [ Time Frame: before and after 12 weeks of intervention ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Muscle strength [ Time Frame: before and after 12 weeks of intervention ] [ Designated as safety issue: No ]
  • Body composition [ Time Frame: before and after 12 weeks of intervention ] [ Designated as safety issue: No ]

Enrollment: 26
Study Start Date: January 2007
Study Completion Date: July 2008
Primary Completion Date: September 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Placebo Comparator
placebo drink
Behavioral: Resistance training
12 weeks resistance training, 3 days per week
2: Experimental
protein drink
Dietary Supplement: protein drink
250 ml protein hydrolysate solution
Behavioral: Resistance training
12 weeks resistance training, 3 days per week

  Eligibility

Ages Eligible for Study:   65 Years to 85 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Living independently

Exclusion Criteria:

  • Diabetes
  • Cardiovascular disease
  • Orthopedic limitations
  • Any disorder known to compromise ability for resistance training
  • History of resistance training in past 5 years
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00744094

Locations
Netherlands
Maastricht University
Maastricht, Netherlands, 6200MD
Sponsors and Collaborators
Maastricht University Medical Center
The Anna Foundation
DSM Food Specialties
Investigators
Principal Investigator: Luc JC van Loon, PhD Maastricht University Medical Center
  More Information

Responsible Party: Maastricht University ( Dr. L. van Loon )
Study ID Numbers: MEC 06-3-062B
Study First Received: August 28, 2008
Last Updated: August 28, 2008
ClinicalTrials.gov Identifier: NCT00744094  
Health Authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by Maastricht University Medical Center:
resistance training
protein supplementation
hypertrophy

Study placed in the following topic categories:
Pathological Conditions, Anatomical
Hypertrophy
Atrophy
Healthy

ClinicalTrials.gov processed this record on January 16, 2009