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

Investigation of the effect of modified rollover footwear on the lower limb kinematics, pain and disability in people with chronic non specific low back pain.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220404054401N1

Enrollment

Registered

2023-12-24

Start date

2023-12-22

Completion date

Unknown

Last updated

2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic non-specific low back pain. Low back pain

Interventions

Intervention 1: Intervention group: The first intervention group will receive rollover shoes with anti-pronation insoles and exercise therapy. The characteristics of the rocker of this shoe are: foref

Eligibility

Sex/Gender

All

Age

18 Years to 50 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Forghany

Esfahan University of Medical Sciences

saeed_forghany@yahoo.co.uk+98 31 3792 5053

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026