Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
61 participants
INTERVENTIONAL
2008-06-30
2012-02-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of GPR on Non-Specific Chronic Low Back Pain
NCT06928597
Postural Re-education in Low Back Pain
NCT00789204
Global Posture Reeducation (GPR) Compared To Isostretching in Chronic Low Back Pain Patients
NCT01468298
Impact of a Balance Reeducation Protocol on Pain, Function and Postural Control of Low Back Pain Patients
NCT01342432
Graded Activity Versus Supervised Exercises in Patients With Chronic Non-specific Low Back Pain
NCT01719276
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Postural Reeducation Group
The participants, after obtaining a written informed consent, were randomized for one of the two groups: In the Global Postural Reeducation group (GPR), they were submitted 1 time per week, during 12 weeks, at GPR sessions. The duration of sessions was 60 minutes each, with the same physical Therapist of the study. After the intervention, subjects returned to assessment 3 months after, with the blinded assessor. All the 6 postures from GPR were used during the study. All outcomes measurements, in both groups, were validated for Portuguese language and applicable at baseline, 3 months and 6 months after baseline.
Global Reeducation Group
They were treated with medication if necessary and performed GPR session once a week, during 12 weeks. All the 6 postures from GPR were used during the study.
Control Group
In the control group, no physical intervention was given during the study. After the study, 6 months after, all participants from control group received the same treatment given in GPR group, according to the Unifesp Ethics Committee orientations. All participants, of both groups, have a doctor from the study, if necessary.
Control Group
No physical intervention was given, patients were treated only with medication if necessary.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Control Group
No physical intervention was given, patients were treated only with medication if necessary.
Global Reeducation Group
They were treated with medication if necessary and performed GPR session once a week, during 12 weeks. All the 6 postures from GPR were used during the study.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* low back pain (more than 12 weeks) without legs irradiation,
* pain between 3-8 cm on a visual Analogue scale (0-10cm).
Exclusion Criteria
* pregnancy,
* osteoporosis severe,
* disc herniation,
* patients who had undergone spinal surgical or physiotherapeutic interventions within 3 months prior to baseline assessment.
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Federal University of São Paulo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Priscila Maria Mendonca de Almeida Lawand
physical therapeutic
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Priscila Maria Lawand, Author
Role: PRINCIPAL_INVESTIGATOR
Federal University of São Paulo
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
São Paulo Federal University UNIFESP
São Paulo, São Paulo, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Postural Global Reeducation Society
São Paulo Federal University
Department of Rheumatology from UNIFESP
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1324/07
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.