Combined Effects of Resistance Training and Nutritional Supplements in the Treatment of Sarcopenia

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Terminated
CT.gov ID
NCT00748696
Collaborator
(none)
2
1
4
24
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Study Details

Study Description

Brief Summary

Age-related sarcopenia is associated with increased morbidity, mortality, disability and reduced resistance to metabolic stress. The aim of this study is to assess the effects of resistance training, associated or not with oral nutritional supplements, on skeletal muscle mass in sarcopenic subjects. This is a prospective randomised controlled single-centre study that will last two years, three months for a participant.

200 healthy elderly (70-80 years old) subjects will be screened for sarcopenia by dual energy

X-ray absorptiometry. 128 sarcopenic subjects will be randomized into 4 groups:
  • group 1: controls

  • group 2: oral nutritional supplement (260 kcal and 20 g protein per day)

  • group 3: resistance training (3 times per week)

  • group 4: oral nutritional supplement + resistance training

Every subject will be assessed at the beginning and at the end of 12 weeks of intervention on:

  • muscle mass (DXA)

  • muscle function (dynamometers)

  • hormonal (testosterone, GH, IGF-1, cortisol) and inflammatory (IL-6, TNF-alpha) profiles

  • food intake. Ten subjects in group 4 will undergo a muscle biopsy (quadriceps) before and after the intervention in order to explore protein and mRNA levels of the mTOR pathway, which may be involved in sarcopenia.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Fortimel Extra®
  • Other: resistance training
  • Other: combined treatment
Phase 3

Detailed Description

Age-related sarcopenia is a common situation defined by muscle mass and function loss in an otherwise healthy elderly person. Epidemiological data from the USA show 49% of men and 72% of women to suffer from sarcopenia. Few data is available on the French population. Sarcopenia is associated with increased morbidity, mortality, disability and reduced resistance to metabolic stress. Resistance training and nutrition are two non-pharmaceutical methods that may be able to prevent several age-related condition.

The aim of this study is to assess the effects of resistance training, associated or not with oral nutritional supplements, on skeletal muscle mass (expressed as skeletal muscle mass index) in sarcopenic subjects. This is a prospective randomised controlled single-centre study that will last two years, three months for a participant.

200 healthy elderly (70-80 years old) subjects will be screened for sarcopenia by dual energy

X-ray absorptiometry. 128 sarcopenic subjects will be randomized into 4 groups:
  • group 1: controls

  • group 2: oral nutritional supplement (260 kcal and 20 g protein per day)

  • group 3: resistance training (3 times per week)

  • group 4: oral nutritional supplement + resistance training

Every subject will be assessed at the beginning and at the end of 12 weeks of intervention on:

  • muscle mass (DXA)

  • muscle function (dynamometers)

  • hormonal (testosterone, GH, IGF-1, cortisol) and inflammatory (IL-6, TNF-alpha) profiles

  • food intake. Ten subjects in group 4 will undergo a muscle biopsy (quadriceps) before and after the intervention in order to explore protein and mRNA levels of the mTOR pathway, which may be involved in sarcopenia.

We expect to show that sarcopenia can be improved by 12 weeks of resistance training and that this improvement can be potentialized by oral nutritional supplements (with a stimulation of the mTOR pathway), and that oral nutritional supplements alone will affect neither muscle mass nor function.

Study Design

Study Type:
Interventional
Actual Enrollment :
2 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Combined Effects of Resistance Training and Nutritional Supplements in the Treatment of Sarcopenia
Study Start Date :
Dec 1, 2006
Actual Primary Completion Date :
Dec 1, 2008
Actual Study Completion Date :
Dec 1, 2008

Arms and Interventions

Arm Intervention/Treatment
No Intervention: 1

No intervention

Experimental: 2

patient receiving oral nutrition supplement

Dietary Supplement: Fortimel Extra®
260kcal and 20g protein per day

Experimental: 3

resistance training

Other: resistance training
3 sessions of resistance training per week

Experimental: 4

patients receiving resistance training and oral nutritional supplement

Other: combined treatment
260kcal and 20g protein per day 3 sessions of resistance training per week

Outcome Measures

Primary Outcome Measures

  1. muscle mass (DXA) [D0 and after 12 weeks]

Secondary Outcome Measures

  1. muscle function (dynamometers), hormonal (testosterone, GH, IGF-1, cortisol) and inflammatory (IL-6, TNF-alpha) profiles, food intake, ± muscle biopsy. [D0 and after 12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
70 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age between 70 and 80 years

  • Stable weight (± 1 kg) during the last three months

  • Informed consent signed

  • Affiliated with the French Sécurité Sociale Non-inclusion criteria

  • Chronic cachectic condition: cancer, chronic respiratory failure, advanced organ failure, hyperthyroidism, rheumatoid arthritis, AIDS, type 1 diabetes

  • Drugs affecting muscle mass (e.g. steroids)

  • Condition (clinical or EKG) significantly affecting physical capacities and/or contra-indicating resistance training

  • Habitual practice of resistance training

  • Habitual intake of nutritional supplements

  • Known coagulation disorders (for muscle biopsy)

  • Known allergy to lidocaine (for muscle biopsy)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of gastroenterology, Department of Gerontology Nice France 06000

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Stephane Schneider, PU PH, Department of Gastroenterology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT00748696
Other Study ID Numbers:
  • 06-API-04
First Posted:
Sep 8, 2008
Last Update Posted:
Feb 22, 2012
Last Verified:
Jun 1, 2009
Keywords provided by Centre Hospitalier Universitaire de Nice
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 22, 2012