Effects Whole Body Vibration in Ergospirometrics Paramete... | NCT01538888

Studies
Effects Whole Body Vibration in Ergospirometrics Parameters and Quality of Life

NCT01538888

Sponsor

Universidade Federal de Pernambuco

Status

Completed

Last Update Posted

Feb 24, 2012Estimated

Enrollment

35Actual

Phase

Phase 1Phase 2

Conditions

Healthy

Interventions

WHOLE BODY VIBRATION

Countries

Brazil

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Feb 2012

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Feb 2011

Primary Completion Date

Feb 2012Actual

Completion Date

Feb 2012Actual

First Submitted Date

Feb 9, 2012

First Submission Date that Met QC Criteria

Feb 18, 2012

First Posted Date

Feb 24, 2012Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Feb 18, 2012

Last Update Posted Date

Feb 24, 2012Estimated

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief 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.

Detailed Description

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

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Phase 1Phase 2

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

35Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
WHOLE BODY VIBRATION	Experimental	SEARCH THE CARDIOPULMONARY EFFECTS IN WHOLE BODY VIBRATION IN HEALTH ELDERLY	Procedure: WHOLE BODY VIBRATION

Interventions

Name	Type	Description	Arm Group Labels	Other Names
WHOLE BODY VIBRATION	Procedure	03 MONTHS, TWICE PER WEEK	WHOLE BODY VIBRATION

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
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

Secondary Outcomes

Measure	Description	Time Frame
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

Other Outcomes

Not provided

Eligibility Module

Eligibility 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

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

60 Years

Maximum Age

74 Years

Standard Ages

AdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Maíra F Pessoa, MS	Universidade Federal de Pernambuco	Study Director
Rafaela B Sá, MS	Universidade Federal de Pernambuco	Study Chair

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Federal University of Pernambuco		Recife	Pernambuco	50670-901	Brazil