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Exercise for Low Back Pain in Children

Not Applicable
Completed
Conditions
Low Back Pain
Interventions
Other: exercise programme
Registration Number
NCT00786864
Lead Sponsor
University of Witwatersrand, South Africa
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1. Experimental Groupexercise programmeExercise Intervention Group
Primary Outcome Measures
NameTimeMethod
Low Back Pain Prevalence3 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 Intensity3 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 Outcome Measures
NameTimeMethod
Neural Mobility3 months post-intervention

Straight leg raise test was used to measure neural mobility. The amount of hip flexion (angle between the plinth and femur of the raised leg) was measured using a digital inclinometer. Scores ranged between 3 (worst score) and 90.5 (best score). Continuous data.

Hamstring Flexibility3 months post-intervention

Standardised hamstring muscle length test. The child was positioned in supine, with the hip flexed at 90 degrees. The knee was then extended passively. The angle of knee extension \[from horizontal plane (level to plinth) to fibula\] was measured using a digital inclinometer. Continuous data. Scores ranged from -20 (worst score) to 82 (best score).

Trial Locations

Locations (1)

Government primary schools in the Ekurhuleni West and Johannesburg East Districts of Gauteng

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Johannesburg, Gauteng, South Africa

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