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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 October 23, 2014