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

The Effect of Trunk Motor Control Exercises Along with Pain Neuroscience Education in Water and Land Environment on Disability, Psychological Variables and Postural Control of Patients with Non-Specific Chronic Low Back Pain: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240311061249N1

Enrollment

Registered

2024-03-30

Start date

2024-01-20

Completion date

Unknown

Last updated

2024-05-27

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: Motor Control Exercises in Four Weeks, 6 Sessions per Week (3 Sessions in the Swimming Pool of Bu-Ali Sina University and 3 Sessions in the Sports hall of Bu-Ali Si

Eligibility

Sex/Gender

Female

Age

30 Years to 60 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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).	—

Measure

Time frame

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).

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Secondary

Measure	Time frame
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).	—

Measure

Time frame

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).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Yalfani

Bu-Ali Sina University, Hamedan

fatemesori1862@gmail.com+98 81 3429 6149

Outcome results

None listed

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