Effects of Global Postural re-Education Program
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|ClinicalTrials.gov Identifier: NCT00736762|
Recruitment Status : Completed
First Posted : August 18, 2008
Last Update Posted : August 18, 2008
The postural alterations present in the seniors people act as predisponent form of incapacities that provoke alterations in the quality of life. The objective of this study is to evaluate the biomechanical characteristics of the balance of elderly people, before and after treatment with Global Postural Re-education. This research is characterized by experimental method of investigation.Thirty elderly people (30 women) will be randomized to two different groups from Group of Studies of Third Age - GETI, at University of the State of Santa Catarina:
- fifteen elderly women will be submitted to the Global Postural Re-education (GPR) program and to the GETI program of activities
- fifteen elderly women will be submitted only to the GETI program of activities.
At baseline the subjects will be screened for balance measurements with the chattecx balance system and Berg Scale. These measurements will be repeat immediately after the intervention. The subjects randomised to the GPR program will participate in posture retraining techniques of approximately forty minutes, one time a week for ten weeks. The independent t test for pairs of random samples will be used, with level of significance of p≤0,05.
|Condition or disease||Intervention/treatment||Phase|
|Healthy Elderly||Other: GPR||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||30 participants|
|Intervention Model:||Parallel Assignment|
|Primary Purpose:||Supportive Care|
|Official Title:||Effects of Global Postural re-Education Program on the Biomechanical Characteristics of the Elderly Balance.|
|Study Start Date :||February 2008|
|Actual Primary Completion Date :||April 2008|
|Actual Study Completion Date :||August 2008|
Global postural re-education intervention
The subjects randomised to the GPR program will participate in posture retraining techniques of approximately forty minutes, one time a week for ten weeks.
- center of pressure (cop) [ Time Frame: pre-treatment, five weeks and pos-treatment ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00736762
|Santa Catarina State University|
|Florianópolis, Santa Catarina, Brazil, 88080350|
|Principal Investigator:||Gilmar Santos, PhD||Santa Catarina State University|