Effects of Motor Imagery on Pain, Function, Endurance, Kinesiophobia and Sleep Quality in Patients With Non-specific Low Back Pain
NCT ID: NCT07237724
Last Updated: 2025-11-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
42 participants
INTERVENTIONAL
2025-11-20
2026-01-16
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Motor imagery (MI) and action observation (AO) offer practical, low-cost approaches that can be easily integrated into rehabilitation programs. Motor imagery involves the individual visualizing the physical movement in their mind without performing it, while action observation involves learning specific movements by observing them. These techniques can strengthen the effectiveness of physical exercises by increasing neuromuscular activation. However, it has been reported that motor imagery-based cortical processes facilitate the reorganization of sensory-motor functions during daily activities in LBP patients. Studies in this area are quite limited. The effectiveness of action observation therapy, which is primarily effective in neurological conditions, has not been investigated in non-specific low back pain. Therefore, in this study, the effects of combining action observation therapy with a core exercise program, Pain, Function, Endurance, Kinesiophobia, and Sleep Quality in patients with non-specific low back pain will be examined.
The study aims to investigate the effects of combining action observation therapy with core exercises compared with core exercises alone in patients with NSLBP. Patients attending Fizyowell physiotherapy and Healthy Services clinic who meet the inclusion criteria will be included in the study. This study seeks to explore the potential benefits of integrating cognitive techniques into a conventional exercise-based rehabilitation for NSLBP.
To establish participant eligibility before the study begins, a standardized demographic data form will be collected from all subjects who volunteered to participate in the study, including gender, age, height, weight, education, marital status, chronic diseases and medication use, smoking, and alcohol use. In addition, the Mini-Mental State Examination (MMSE) will be used to assess the patient's mental state, determine the ability to understand and follow instructions, and identify cognitive disorders that may make it difficult to perform mental interventions. The Movement Imagery Questionnaire-3 (MIQ-3) will be used to determine each participant's motor imagery ability. Once eligibility is confirmed, baseline assessments will be conducted, including pain intensity measured by the Visual Analog Scale (VAS), functional disability assessed using the Oswestry Low Back Pain Disability Index Questionnaire, kinesiophobia evaluated with the Tampa Scale for Kinesiophobia (TSK), core endurance tested through standardized endurance measures, and sleep quality assessed using the Pittsburgh Sleep Quality Index (PSQI).
After the initial evaluation, the treatment program will be started. Advances in the treatment method specific to the groups they belong to are explained in detail below.
Treatment:
After the first evaluation, the core exercise program will be applied to the patients in Group 1, 3 days per week for 6 weeks. All sessions will be conducted under the supervision of a physiotherapist at the clinic.
Group 2: Conservative Treatment + Action Observation Program. This group will have action observation therapy in addition to the core exercise program. The patients in this group will receive an action observation therapy for 6 minutes before each exercise therapy session. They will watch videos of 2 different activities, the duration of each video is 3 minutes, and they were recorded from 3 planes (frontal, back, and lateral).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Motor Imagery Training in Non-Specific Low Back Pain
NCT06859645
Impact of Motor Imagery in the Functional Rehabilitation of Patients With Chronic Low Back Pain: a Randomised Controlled Trial
NCT07111286
Telerehabilitation-based Motor Imagery in Nonspecific Low Back Pain
NCT05049772
The Effect of Exercise on Motion Perception and Fear in Low Back Pain
NCT05433311
Effectiveness of Perturbation Training in Nonspecific Low Back Pain
NCT06156163
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Core Exercise Program
Participants receive supervised core exercise therapy 3 times per week for 6 weeks.
Core Exercise Program
* The patients will do their exercises at the clinic as face to face sessions. All sessions will be conducted under the supervision of a physiotherapist
* patients will receive core exercises program, 3 days per week
* Treatment duration is 6 weeks
Core Exercise + Action Observation
Participants receive the same core exercise therapy plus an action observation session before each treatment.
Action Observation Therapy
* The patients will do their exercises at the clinic as face to face sessions. All sessions will be conducted under the supervision of a physiotherapist
* patients will receive the same core exercises program as the Active comparator group, 3 days per week for 6 weeks
* This group will receive action observation therapy for 6 minutes before every exercise therapy session. they will watch videos of 2 different activates, the duration of each video is 3 minutes and will be recorded from 3 planes (front, back and lateral )
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Core Exercise Program
* The patients will do their exercises at the clinic as face to face sessions. All sessions will be conducted under the supervision of a physiotherapist
* patients will receive core exercises program, 3 days per week
* Treatment duration is 6 weeks
Action Observation Therapy
* The patients will do their exercises at the clinic as face to face sessions. All sessions will be conducted under the supervision of a physiotherapist
* patients will receive the same core exercises program as the Active comparator group, 3 days per week for 6 weeks
* This group will receive action observation therapy for 6 minutes before every exercise therapy session. they will watch videos of 2 different activates, the duration of each video is 3 minutes and will be recorded from 3 planes (front, back and lateral )
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being a volunteer.
* Having nonspecific chronic low back pain for three months or more.
* No obvious structural or anatomical abnormality that could explain the pain.
* Scoring 24 or more out of 30 on the Mini-Mental State Examination.
* Those who score high in terms of imagery ability on the MIQ-3 questionnaire.
* Not having any pathology in vision or hearing
Exclusion Criteria
* Having a painful spinal deformity.
* Having a spinal surgery
* Having a mental illness and/or communication problem.
* Having pain radiating to the lower extremity.
* Having any back disease diagnosed by a specialist physician other than non-specific chronic back pain
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Bahçeşehir University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sara Hamdi Mohamed Kamal Shalabi
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sara Hamdi Shalabi
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Salik Sengul Y, Kaya N, Yalcinkaya G, Kirmizi M, Kalemci O. The effects of the addition of motor imagery to home exercises on pain, disability and psychosocial parameters in patients undergoing lumbar spinal surgery: A randomized controlled trial. Explore (NY). 2021 Jul-Aug;17(4):334-339. doi: 10.1016/j.explore.2020.02.001. Epub 2020 Feb 22.
Ozturk O, Bombaci H, Kececi T, Algun ZC. Effects of additional action observation to an exercise program in patients with chronic pain due to knee osteoarthritis: A randomized-controlled trial. Musculoskelet Sci Pract. 2021 Apr;52:102334. doi: 10.1016/j.msksp.2021.102334. Epub 2021 Jan 24.
Salik Sengul Y, Yilmaz A, Kirmizi M, Kahraman T, Kalemci O. Effects of stabilization exercises on disability, pain, and core stability in patients with non-specific low back pain: A randomized controlled trial. Work. 2021;70(1):99-107. doi: 10.3233/WOR-213557.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
61351342/020-65
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.