Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 12:43 AM
NCT ID:
NCT02175667
Brief Summary:
Determine the influence of a treatment with Global Postural Reeducation techniques and the personality traits in the stabilometric parameters
Detailed Description:
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)
Study:
NCT02175667
Study Brief:
Protocol Section:
NCT02175667