Effects Whole Body Vibration in Ergospirometrics Parameters and Quality of Life (EWBVEPQL)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Maíra F Pessoa, Universidade Federal de Pernambuco
ClinicalTrials.gov Identifier:
NCT01538888
First received: February 9, 2012
Last updated: February 18, 2012
Last verified: February 2012
  Purpose

This study makes sure that the training of whole body vibration induces changes in ergospirometric parameters, in strength and influence in quality of life in healthy elderly. A case that is run like a vibration training combined, increasing strength and VO2.


Condition Intervention Phase
Healthy
Procedure: WHOLE BODY VIBRATION
Phase 1
Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: Effects Whole Body Vibration in Ergospirometrics Parameters, Strength And Quality of Life: A Randomised Controlled Trial

Further study details as provided by Universidade Federal de Pernambuco:

Primary Outcome Measures:
  • VO2 [ Time Frame: 03 MONTHS IN INTERVENTION ] [ Designated as safety issue: No ]
    change to maximal oxygen consumption (ml.kg.min)in ergospirometric test after 03 months training in vibrating platform twice per weeck.


Secondary Outcome Measures:
  • quality of life [ Time Frame: 03 month ] [ Designated as safety issue: No ]
    outcome measure with the SF 36 shot form (Medical Outcomes Study 36 - Item short form health survey)after 03 months training in vibrating platform twice per weeck


Enrollment: 35
Study Start Date: February 2011
Study Completion Date: February 2012
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: WHOLE BODY VIBRATION
SEARCH THE CARDIOPULMONARY EFFECTS IN WHOLE BODY VIBRATION IN HEALTH ELDERLY
Procedure: WHOLE BODY VIBRATION
03 MONTHS, TWICE PER WEEK
Other Name: POWER PLATE, MODEL MY3

Detailed Description:

The search use the spirometric values after whole body vibration training and resistance training

  Eligibility

Ages Eligible for Study:   60 Years to 74 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • aged 60 to 74 years
  • sedentary or irregularly active according to the IPAQ short form with no known diseases

Exclusion Criteria:

  • smoking
  • acute hernia
  • thrombosis
  • labyrinthitis
  • diabetes
  • hemodynamic instability
  • obesity
  • osteoporosis
  • neuromuscular diseases
  • pulmonary comorbidities
  • heart disease
  • electrocardiographic changes during exercise
  • taking medications that affected bone metabolism or muscle and don't adapt to any of the protocols
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01538888

Locations
Brazil
Federal University of Pernambuco
Recife, Pernambuco, Brazil, 50670-901
Sponsors and Collaborators
Universidade Federal de Pernambuco
Investigators
Study Director: Maíra F Pessoa, MS Universidade Federal de Pernambuco
Study Chair: Rafaela B Sá, MS Universidade Federal de Pernambuco
  More Information

No publications provided

Responsible Party: Maíra F Pessoa, graduate, Universidade Federal de Pernambuco
ClinicalTrials.gov Identifier: NCT01538888     History of Changes
Other Study ID Numbers: EQ1
Study First Received: February 9, 2012
Last Updated: February 18, 2012
Health Authority: BRAZIL: UFPernambuco

Keywords provided by Universidade Federal de Pernambuco:
WHOLE BODY VIBRATION
AGED
VO2
aged
muscle strength

ClinicalTrials.gov processed this record on April 22, 2014