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Clinical Trials/NCT00600197
NCT00600197UnknownNot Applicable

The Effectiveness of Biopsychosocial Education on Quality of Life and Disability of Individuals Suffering From Chronic Low Back Pain

Tehran University of Medical Sciences1 site in 1 country170 target enrollmentStarted: July 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
170
Locations
1
Primary Endpoint
SF-36, Roland Morris Disability Questionnaire, Quebec back pain disability

Study Overview

Brief Summary

The purpose of this study is to examine whether the biopsychosocial educational program could improve patients' health-related quality of life at 3-6-12-18-24-30 and 36 - month follow up.

Detailed Description

Little information exists on biopsychosocial educational program as a multidimensional and interdisciplinary program in which Quality Of Life is as an outcome measure. Thus this educational Program designed in this study is a an outpatient program that used a health education approach to empower participants through a process of assessment, education and skill building in three dimensions of physical,mental and social that leading to improved quality of life. The purpose of this study was to examine to what extent this educational Program could improve low back pain patients' HRQOL.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Low Back Pain lasting more than 12 weeks with or without pain radiating to the legs.
  • age 18-70 years.

Exclusion Criteria

  • Osteoporosis
  • Newly operation on the back up to 2 years before the beginning of the study
  • Fresh vertebral fracture
  • Malignancy
  • Infection in the back
  • spondylolisthesis
  • Problem in understanding Farsi Language

Outcomes

Primary Outcomes

SF-36, Roland Morris Disability Questionnaire, Quebec back pain disability

Time Frame: before intervention

Secondary Outcomes

  • SF-36,Roland Morris Disability Questionnaire, Quebec back pain disability(3-6-12-18-24-30-36 month after intervention)

Investigators

Sponsor Class
Other

Study Sites (1)

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