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Clinical Trials/NCT00786864
NCT00786864
Completed
N/A

School-Based Specific Exercise Programme Reduces the Prevalence and Intensity of Low Back Pain in 12-13 Year Old Children: a Randomized Controlled Trial

University of Witwatersrand, South Africa1 site in 1 country72 target enrollmentJanuary 2007
ConditionsLow Back Pain

Overview

Phase
N/A
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
University of Witwatersrand, South Africa
Enrollment
72
Locations
1
Primary Endpoint
Low Back Pain Prevalence
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

This study aimed to determine the efficacy of an eight-week specific exercise programme in reducing self-reported episodes and intensity of LBP, as well as modifying some of the identified risk factors for LBP, in children.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
October 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Witwatersrand, South Africa

Eligibility Criteria

Inclusion Criteria

  • Children aged 12-13 years
  • Complained of LBP in the past three months

Exclusion Criteria

  • Serious spinal pathologies or deformities (e.g. severe scoliosis, spinal tumours)
  • Neurological conditions which alter motor tone
  • Physical disabilities (e.g. spinal cord injuries) which prevent the child from being able to stand up on their own without an orthotic device or brace, or which prevent the child from taking part in normal physical education (PE) classes
  • Any other serious co-morbidities (e.g. cancer, severe lung pathology)
  • Provincial sports participants, or children who were currently following a specific training programme with a biokineticist or physiotherapist
  • Current orthopaedic procedures or fractures of the spine, pelvis, lower or upper limbs

Outcomes

Primary Outcomes

Low Back Pain Prevalence

Time Frame: 3 months post-intervention

All of the children complained of low back pain at baseline. Low back pain prevalence post-intervention was determined by the number of children still complaining of low back pain post-intervention.

Low Back Pain Intensity

Time Frame: 3 months post-intervention

The visual analogue scale (standardised 100mm, non-hatched line) was used to determine pain intensity. Scores can range between 0 and 10, with the worst possible pain/score = 10 and no pain/best score = 0. Visual analogue scale is continuous.

Secondary Outcomes

  • Neural Mobility(3 months post-intervention)
  • Hamstring Flexibility(3 months post-intervention)

Study Sites (1)

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