Comparison of two methods of core stability exercises to improve chronic low back pai

Not Applicable

• Conditions: Chronic non-specific back pain.; Back pain; M54.5

• Registration Number: IRCT20180727040609N2
• Lead Sponsor: Shahid Beheshti University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

People with non-specific chronic back pain
Absence of any history of spine surgery
Absence of pathological records (disease) of the spine
Absence of orthopedic and neurological injuries
Absence of structural or functional shortness of more than 2 cm in one of the lower limbs

Exclusion Criteria

The presence of the lumbar disc herniation
The presence of the acute stage of lumbar disc protrusion
The presence of the systematic diseases (such as cardiovascular)
Spine surgery in the past
Having a fracture or inflammatory diseases of the spine
Having any therapeutic intervention in the last two months
Taking medical drugs
Failure to participate in the treatment sessions

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: 8 weeks. The pain variable will be evaluated one day before the start and one day after the end of the research/treatment period. Method of measurement: Pain (Using Visual Analog Scale; VAS ).;Functional disability. Timepoint: 8 weeks. The functional disability variable will be evaluated one day before the start and one day after the end of the research/treatment period. Method of measurement: Functional disability (Using Oswestry questionnaire).

Secondary Outcome Measures

Name	Time	Method
Pain. Timepoint: 8 weeks. The pain variable will be evaluated one day before the start and one day after the end of the research/treatment period. Method of measurement: The visual analogue scale (VAS).;Functional disability. Timepoint: En 8 weeks. The functional disability variable will be evaluated one day before the start and one day after the end of the research/treatment period. Method of measurement: Functional disability (Using Oswestry questionnaire).