Effects Whole Body Vibration in Ergospirometrics Parameters and Quality of Life

Healthy Clinical Trial

— EWBVEPQL  

Official title:

Effects Whole Body Vibration in Ergospirometrics Parameters, Strength And Quality of Life: A Randomised Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01538888
• Other study ID #: EQ1
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: February 9, 2012
• Last updated: February 18, 2012
• Start date: February 2011
• Est. completion date: February 2012

Study information

• Verified date: February 2012
• Source: Universidade Federal de Pernambuco
• Contact: n/a
• Is FDA regulated: No
• Health authority: BRAZIL: UFPernambuco
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: February 2012
• Est. primary completion date: February 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 60 Years to 74 Years

Eligibility

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

Study Design

Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Healthy

Intervention

Procedure:
• WHOLE BODY VIBRATION
03 MONTHS, TWICE PER WEEK

Locations

Country	Name	City	State
Brazil	Federal University of Pernambuco	Recife	Pernambuco

Sponsors (1)

Lead Sponsor	Collaborator
Universidade Federal de Pernambuco

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	VO2	change to maximal oxygen consumption (ml.kg.min)in ergospirometric test after 03 months training in vibrating platform twice per weeck.	03 MONTHS IN INTERVENTION	No
Secondary	quality of life	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	03 month	No