Effectiveness of Global Postural Reeducation in Patients With Chronic Symptomatic Lumbar Disc Herniation

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2010 by Universidade Gama Filho.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Universidade Gama Filho
ClinicalTrials.gov Identifier:
NCT01236924
First received: November 8, 2010
Last updated: NA
Last verified: November 2010
History: No changes posted
  Purpose

Slipped disc is the rupture of the fibrous ring, with subsequent displacement of the nucleus pulposus in intervertebral spaces, which may cause compression of nerve structures. It is estimated that 2-3% of the population have taken with this process, whose prevalence is 4.8% in men and 2.5% in women over 35 years. Thus, the purpose of this study is to verify the effectiveness of global postural reeducation in patients diagnosed with chronic symptomatic lumbar disc herniation with the application of a randomized controlled trial. Will be measured pain, disability and functional flexibility.


Condition Intervention Phase
Lumbar Disc Herniation.
Other: Global postural reeducation
Phase 1

Study Type: Interventional
Study Design: Primary Purpose: Treatment
Official Title: Effectiveness of Global Postural Reeducation in Patients With Chronic Symptomatic Lumbar Disc Herniation

Resource links provided by NLM:


Further study details as provided by Universidade Gama Filho:

Study Start Date: January 2011
Arms Assigned Interventions
Experimental: Lifestyle counseling Other: Global postural reeducation

  Eligibility

Ages Eligible for Study:   25 Years to 45 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Patients diagnosed with chronic symptomatic lumbar disc herniation

Exclusion Criteria:

Patients who work with severe overloading of the spine, patients with central neurological pathology, wheelchair users, patients who use bracing and support those who submit two consecutive absences to the treatment

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01236924

Locations
Brazil
Gama Filho University
Rio de Janeiro, RJ, Brazil
Sponsors and Collaborators
Universidade Gama Filho
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01236924     History of Changes
Other Study ID Numbers: 112.2010
Study First Received: November 8, 2010
Last Updated: November 8, 2010
Health Authority: Brazil: National Health Council

Additional relevant MeSH terms:
Hernia
Intervertebral Disc Displacement
Pathological Conditions, Anatomical
Spinal Diseases
Bone Diseases
Musculoskeletal Diseases

ClinicalTrials.gov processed this record on September 22, 2014