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Investigation of the effect of modified rollover footwear in chronic non specific low back pain.

Not Applicable
Recruiting
Conditions
chronic non-specific low back pain.
Low back pain
M54.5
Registration Number
IRCT20220404054401N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
33
Inclusion Criteria

Duration of pain more than 12 weeks and bilaterally
The existence of a minimum score of 3 for the pain parameter based on the visual analog scale
medium risk subgroup based on the Subgroups for Targeted Treatment Back Screening Tool questionnaire
Daily use of shoes for at least 6 hours

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before the starting of the intervention and 6 weeks after the starting of the intervention. Method of measurement: Visual Analogue Scale.;Disability. Timepoint: Before the starting of the intervention and 6 weeks after the starting of the intervention. Method of measurement: Roland-Morris Disability Questionnaire.;Angles of the lower limb joints. Timepoint: Before the starting of the intervention and 6 weeks after the starting of the intervention. Method of measurement: Qualysis motion analysis system.
Secondary Outcome Measures
NameTimeMethod
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