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Postural; DefectRPG-POSTURENCT02175667

Influence of the Global Postural Reeducation and the Personality in the Posture

A study testing Global Postural Reeducation in people with Postural; Defect, run by Universidad Miguel Hernandez de Elche at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Determine the influence of a treatment with Global Postural Reeducation techniques and the personality traits in the stabilometric parameters Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Postural; Defect
What is being tested?
Global Postural Reeducation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
76 participants
Where
1 siteSpain
Study dates
Jul 2014to Oct 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • College students spend 4 hours or more per day sitting

Who cannot join

  • College students do not spend 4 hours or more per day sitting.
  • Subjects with a traumatic problem, injuries, in the moment of the study, or subject in treatment of this injuries

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Miguel Hernández University of Elche

    Sant Joan, Alicante, 03550

Other trials in Spain

About this study

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

Read the 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)

Being tested
Global Postural Reeducation
Keywords
Global postural reeducation, Stabilometry, Postural Sway, Range of motion, Personality traits

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Global Postural ReeducationProcedure or surgery

    Also called Manual Therapy, Muscle chains, Stretching

    Experimental group is treated in a 45 minutes GPR session, with three postures: the first was for 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 table. This posture is maintained 25-30 minutes. The second GPR posture, to stretch the posterior muscle chain, the participant is positioned with legs elevated, for 12-15 minutes. Third position is with the participant standing and 2-5 minutes to integrate the postural corrections. During all the time, the physiotherapist use manual therapy for stretch the muscles under the official rules of GPR techniques. Group control do not receive any technique.

Study groups in NCT02175667
Study groupRoleWhat they receive
Global Postural ReeducationExperimentalParticipants receiving GPR treatment during 45 minutes to stretch muscular chains
Receives: Procedure: Global Postural Reeducation
ControlNo interventionParticipants not receiving GPR treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Centre of pressure displacement in standing position

    Displacement antero-posterior and lateral of COP measured with a platform of pressures

    Measured: Before intervention, 2 minutes after, 2 days after, 7 days after

Secondary outcomes (3)
  1. Plantar pressures distribution in standing position

    Plantar pressures distribution in each foot measured with a platform of pressures

    Measured: Before intervention, 2 minutes after, 2 days after, 7 days after

  2. Percentage of load distribution in standing position

    Load distribution between feet measured with a platform of pressures

    Measured: Before intervention, 2 minutes after, 2 days after, 7 days after

  3. Lumbar and cervical range of motion

    Cervical and lumbar inclinometer for goniometry

    Measured: Before intervention, 10 minutes after, 2 days after, 7 days after

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2014 (estimated)
  2. Study startJul 2014
  3. Primary completionOct 2014
  4. Study completionOct 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
76 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02175667
Sponsor's protocol ID
DPC-CLQ-001-12
Acronym
RPG-POSTURE
Status last verified
Oct 2014
First submitted
16 Jun 2014
Last updated
17 Dec 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Global Postural Reeducation in people with Postural; Defect, run by Universidad Miguel Hernandez de Elche at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Dec 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Centre of pressure displacement in standing position (time frame: Before intervention, 2 minutes after, 2 days after, 7 days after). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2015; AzTrials last refreshed its copy on 8 Nov 2026.

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