Postural; Defect Clinical Trial
Official title:
Influence of the Global Postural Reeducation and the Personality Traits in the Range of Motion, in the Stabilometry and in the Postural Sway.
Determine the influence of a treatment with Global Postural Reeducation techniques and the personality traits in the stabilometric parameters
This study is realized with university students. For a first objective of this study, all
the participants complete the "big five questionnaire" to determine their personality traits
and then the subjects are analyzed with a stabilometric platform and cervical/lumbar range
of motion (ROM) to determine their basal parameters. The personality traits and the basal
stabilometric parameters like the postural sway, will be crossed to investigate a possible
relation. For a second objective, the randomized study of the effectiveness of the Global
Postural Reeducation (GPR) in the stabilometric parameters, the subjects are divided in a
experimental group or in a control group. Experimental group is treated in a 45 minutes GPR
session, with three postures: the first is for stretch the anterior muscular chain with the
patient lying supine on a couch with arms at 45 degrees, hips open, and feet in opposition
on top of the couch. This posture is maintained 25-30 minutes. In the second GPR posture, to
stretch the posterior muscular chain, the subject is positioned with legs elevated, for
12-15 minutes. Third position is with the participant in upright standing posture 2-5
minutes to integrate the postural corrections. During all the time, the physiotherapist uses
manual therapy for stretch the muscles under the official rules of GPR techniques. Group
control do not receive any technique. After the time of the intervention or no intervention,
a second measure of stabilometric parameters and ROM is taken. After this first day, two
days later and seven days later, the measures are repeated to determinate the permanence of
the effects of GPR techniques.
The improvement will be assessed by calculating indicators of clinical relevance: relative
risk (RR), absolute risk reduction (AR). The results will be compared statistically to
determine some possible relation. The confidence intervals (CI) will be calculated for the
most relevant parameters. The analysis will be made with a statistics program (SPSS 19.0)
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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