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Comparison Two Manual Therapy Techniques and Balance Training in Patients with Low Back Pai

Not Applicable
Conditions
ow Back Pain.
Low back pain
Registration Number
IRCT20170117032020N3
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
Inclusion Criteria

Presence of back pain (from below the costal margin to inferior gluteal folds) for more than 3 months
Pain intensity between 3 and 6 based on visual analogue scale
Pain reduction through reduce the strain on affected segment

Exclusion Criteria

Presence of symptoms such as Neurological pain, Non-mechanical pain, and General Pain
Severe muscle weakness
Presence of significant scoliosis
History of Spinal surgery
Pregnancy during study
spondylolisthesis
Inflammatory diseases

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Center of pressure displacement. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Force Platform.;Mean of Anterior-posterior Center of pressure location. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Force Platform.;Mean of medial-lateral Center of pressure location. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Force Platform.;Center of pressure displacement velocity. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Force Platform.
Secondary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Visual Analogue Scale.;Ostwestry Disability Index. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Ostwestry Disability Questionnaire.;Depression Score. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Beck Depression Inventory-II.;Quality of Life score. Timepoint: Before intervention, 5 weeks after, and 2 months follow-up. Method of measurement: Short-form 36 Questionnaire of Quality of Life.
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