The Long-term Effects of Training on Muscle Strength and Functionality

Sponsor
Universitaire Ziekenhuizen Leuven (Other)
Overall Status
Completed
CT.gov ID
NCT01682330
Collaborator
(none)
65
30

Study Details

Study Description

Brief Summary

The purpose of the present study is to evaluate the long-term effects of 1 year of high-intensity fitness training and low-intensity whole-body vibration training on muscle strength and functionality. Therefore, muscle strength and functionality are measured after a 6-yr interval in older adults (65+).

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    65 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Study Start Date :
    Nov 1, 2011
    Actual Primary Completion Date :
    Dec 1, 2011
    Actual Study Completion Date :
    Dec 1, 2011

    Arms and Interventions

    Arm Intervention/Treatment
    Fitness

    Whole-body vibration

    Control

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      65 Years and Older
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • female (+65 years)

      • participation in previous study "De effecten van oefenprogramma's op gezondheids- en fitheidsgerelateerde parameters in een groep van 60-plussers" [The effects of exercise programs on health and fitness-related parameters in a group of people over 60]

      • able to perform a maximal strength test on a dynamometer

      Exclusion Criteria:
      • pathologies that prohibit a maximal strength test on a dynamometer

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • Universitaire Ziekenhuizen Leuven

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Universitaire Ziekenhuizen Leuven
      ClinicalTrials.gov Identifier:
      NCT01682330
      Other Study ID Numbers:
      • s53571
      First Posted:
      Sep 10, 2012
      Last Update Posted:
      Sep 10, 2012
      Last Verified:
      Jun 1, 2012

      Study Results

      No Results Posted as of Sep 10, 2012