Investigating the effect of motor motor control, neurological and cognitive exercises on non-specific chronic back pai

Not Applicable

Recruiting

Conditions: Chronic non-specific back pain.
Contusion of lower back and pelvis, sequela
S30.0XXS

Registration Number: IRCT20230430058033N1

Lead Sponsor: The University of Bu Ali Sina

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 100

Inclusion Criteria

Women between the ages of 30 and 60
Diagnosis and confirmation of non-specific chronic back pain by a specialist doctor
Not participating in other sports activities
Presence of at least two movement control disorders in Lomajoki movement control tests

Exclusion Criteria

Having a history of injury in the past year in the trunk and lower limbs
A history of surgery in the back and lower limbs
People with back pain of non-mechanical origin
Participants if they have already experienced neurofeedback

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Muscle activity. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: EMG A device for measuring muscle activity.;Vertical earth reaction force. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Foot pressure measuring device.;Brain Waves. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Neurofeedback device.;Cognitive function. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Fully listening to the patient in order to widely identify multidimensional stimuli that can change pain and disability (cognitive behaviors that trigger pain, movement, and lifestyle).

Secondary Outcome Measures

Name	Time	Method
Visual measurement of pain. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Use the Visual Analogue Scale.;Disability. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Oswestry Disability Questionnaire.;Quality of Life. Timepoint: At the beginning of the study before the interventions and 60 days after the exercises. Method of measurement: Shernborn SF36 Questionnaire.