- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01538888
Effects Whole Body Vibration in Ergospirometrics Parameters and Quality of Life (EWBVEPQL)
February 18, 2012 updated by: Maíra F Pessoa, Universidade Federal de Pernambuco
Effects Whole Body Vibration in Ergospirometrics Parameters, Strength And Quality of Life: A Randomised Controlled Trial
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.
Study Overview
Detailed Description
The search use the spirometric values after whole body vibration training and resistance training
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pernambuco
-
Recife, Pernambuco, Brazil, 50670-901
- Federal University of Pernambuco
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years to 74 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: WHOLE BODY VIBRATION
SEARCH THE CARDIOPULMONARY EFFECTS IN WHOLE BODY VIBRATION IN HEALTH ELDERLY
|
03 MONTHS, TWICE PER WEEK
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
VO2
Time Frame: 03 MONTHS IN INTERVENTION
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
quality of life
Time Frame: 03 month
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Maíra F Pessoa, MS, Universidade Federal de Pernambuco
- Study Chair: Rafaela B Sá, MS, Universidade Federal de Pernambuco
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2011
Primary Completion (Actual)
February 1, 2012
Study Completion (Actual)
February 1, 2012
Study Registration Dates
First Submitted
February 9, 2012
First Submitted That Met QC Criteria
February 18, 2012
First Posted (Estimate)
February 24, 2012
Study Record Updates
Last Update Posted (Estimate)
February 24, 2012
Last Update Submitted That Met QC Criteria
February 18, 2012
Last Verified
February 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- EQ1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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