The Effect of Trunk Motor Control Exercises Along with Pain Neuroscience Education in Patients with Non-Specific Chronic Low Back Pai

Phase 3

Conditions: Chronic Non-Specific Low Back Pain.
Low Back Pain
M54.5

Registration Number: IRCT20240311061249N1

Lead Sponsor: Bu-Ali Sina University, Hamedan

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: Female

Target Recruitment: 90

Inclusion Criteria

Suffering from Chronic Low Back Pain for More than 3 Months
The Cause of Low Back Pain is Unknown
Age Range from 30 to 60 Years
Pain Intensity more than 45 mm on the Visual Analog Scale
Oswestrian Disability Index More than 25

Exclusion Criteria

Pain in other Joints
Misalignment of Upper and Lower Limbs
History of Surgery
Use of Painkillers in the Past 6 Months
Physiotherapy in the Last Year
Participate in Sports
Sciatica Pain
Spondylolysis
Neuromuscular Disorders
Neurological Disorder
Respiratory Disorders
Muscle Spasm
Vertebral Fractures

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain, Fear of Movement, Stress, Anxiety, Depression, Pain Catastrophizing. Timepoint: In this Clinical Trial, the Researcher Intends to Evaluate the Variables of Pain, Fear of Movement, Stress, Anxiety, Depression, Pain Catastrophizing in Two time Periods Before the Intervention (Pre-Test) and After the Intervention (4 and 8 Weeks). Method of measurement: Pain (Visual Analog Scale), Fear of Movement (Tampa Questionnaire), Stress, Anxiety and Depression (Stress, Anxiety and Depression Questionnaire), Pain Catastrophizing (Pain Catastrophizing Questionnaire).

Secondary Outcome Measures

Name	Time	Method
Disability, Postural Control, Plantar Pressure Distribution, Vertical Ground Reaction Force. Timepoint: In this Clinical trial, the Researcher Intends to Evaluate Disability Variables, Posture Control, Plantar Pressure Distribution, Vertical Ground Reaction Force in two time Periods before the Intervention (Pre-Test) and after the Intervention (4 and 8 Weeks). Method of measurement: Disability (Oswestory Questionnaire), Posture Control, Plantar Pressure Distribution and Vertical Ground Reaction Force (Foot Pressure).