The Effect of Core Stabilization Exercises in People With Chronic Low Back Pain

March 21, 2022 updated by: Mehmet Akif Guler

The Effect of Core Stabilization Exercises on Pain Level, Functionality, Stability and Lumbar Multifidus Muscle Cross-sectional Area in People With Chronic Low Back Pain

Low back pain is a health problem that causes clinical, social and economic losses all over the world and affects the majority of the population. More than 80% of adults in the general population experience low back pain at least once in their lifetime. Although the incidence of chronic low back pain is so high, 85% of these pains do not have a pathoanatomical cause and these pains are defined as non-specific chronic low back pain. Exercise therapy is the key to the conservative management of nonspecific chronic low back pain. Lumbar stabilization exercises based on the principle of motor control of core muscles have also become popular in rehabilitation programs for low back pain in recent years.The core region is the lumbopelvic region of the body. The aim of the stabilization exercises is to teach to use the neutral position of the lumbar region and to keep the load on the dynamic and static structures at the lowest level. Core stabilization training begins with teaching the contraction of the transversus abdominus, deep spinal and multifidus muscle.Then, these exercises are planned specifically for the person from immobile positions to movements positions, from simple movements to combined movements, from gross patterns to fine motor patterns, from symmetrical movements to asymmetric movements. These exercises can be developed specifically for the region and pathology with the functions of the muscles in the region of the pathology. The lumbar multifidus muscle is known to be an important stabilizer of the lumbar region. In addition, the cross-sectional area of the lumbar multifidus muscle has short, thick, dense muscle fibers compared to other lumbar region muscles.These dense muscle fibers are compressed in a small space and have a high mass.This morphology allows the lumbar multifidus muscle to produce great force in a small working area and makes the muscle ideal for stability. In addition, the position of the lumbar multifidus muscle between the vertebrae increases its importance for stability. The aim of this study is to determine the effects of core stabilization exercises on the cross-sectional area (CSA) and amount of adipose tissue of the lumbar multifidus muscle in adults with chronic low back pain using magnetic resonance imaging (MRI), and also to examine the effects of these exercises on pain, functionality and lumbopelvic stability.

Study Overview

Status

Not yet recruiting

Study Type

Interventional

Enrollment (Anticipated)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Selcuklu
      • Konya, Selcuklu, Turkey, 42131
        • Selcuk University, Faculty of Medicine, Department of Physical Medicine and Rehabilitation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patient with low back pain for at least 3 months or more
  • Age between 18 and 65 years
  • Ability to give informed consent

Exclusion Criteria:

  • History of previous previous spinal surgery
  • Disc herniation with radiculopathy
  • Pregnant or breastfeeding
  • Systemic disease
  • Low back pain due to specific and known causes (Spondylolisthesis, Spinal stenosis, Spondylolysis, Ankylosing spondylitis, Tumor, Structural deformity, Osteoporosis, Rheumatological disease, Infection)
  • History of malignancies/cancer
  • Unexplained or unintentional weight loss
  • Perineal numbness, Bladder dysfunction
  • Progressive weakness in lower limbs
  • Fracture
  • Fever
  • Cauda equina syndrome

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Core Exercise Group
Core Exercise Group will performe core stabilization exercises and routine physiotherapy exercises.

Core Exercise Group Procedure:

Weeks 1-4 (Five days a week)

  1. Hotpack ultrasound, conventional TENS, stretching exercises and strengthening exercises for low back pain.
  2. Core stabilization exercise :

    • Active pelvic floor exercise (supine position)
    • Bridge exercise (supine position)
    • Back Extension and Ball Back Extension exercises (prone position)
    • Abdominal and Oblique Crunch exercises (supin position)
    • Leg lift exercise (prone position)
    • Plank and Side Plank exercise
    • Superman exercise

Weeks 5-8 (Three days a week)

  1. Stretching exercises and strengthening exercises for low back pain.
  2. Core stabilization exercise :

    • The same exercises as for Weeks 1-4 will perform.
Active Comparator: Routine Therapy Group
Routine Therapy Group will performe routine physiotherapy exercises.

Routine Therapy Group Procedure:

Weeks 1-4 (Five days a week)

1. Hotpack ultrasound, conventional TENS, stretching exercises and strengthening exercises for low back pain.

Weeks 5-8 (Three days a week)

1.Stretching exercises and strengthening exercises for low back pain.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measurement of the amount of adipose tissue and CSA of the muscle by MRI
Time Frame: Baseline - End of the eighth week
Axial images obtained from the multi-point DIXON (mDIXON) sequence will be used to determine the cross-sectional area and amount of adipose tissue of the lumbar multifidus muscle. The bilateral cross-sectional areas of the lumbar multifidus muscle from the L1-2, L2-3, L3-4, L4-5 and L5-S1 intervertebral disc levels will be calculated by drawing the outlines of the fascial borders of the muscles. Muscle CSA and amount of adipose tissue will be calculated. Subtracting the amount of adipose tissue from the CSA resulting in the functional CSA of the muscle. There will be two measurements, at baseline before the start of program and at the end of the eight weeks intervention.
Baseline - End of the eighth week
Visual Analog Scale
Time Frame: Baseline - End of the eighth week
Pain will be measured using a 10 cm visual analog scale (VAS). Min pain score is 0, max pain score is 10. Participants will mark a point on the VAS that matches the amount of pain they feel.
Baseline - End of the eighth week
Oswestry Disability Index
Time Frame: Baseline - End of the eighth week

Oswestry Disability Index evaluates the extent to which the patient's level of function is restricted by the pain.. Oswestry Disability Index consists of 10 sections, each section the total possible score is ranging from 0 to 5. The score obtained from all questions is added and multiplied by two. The result is noted as a percentage.

  • 0% to 20%= Minimal disability
  • 21% to 40%= Moderate disability
  • 41% to 60%= Severe disability
  • 61% to 80%= Crippling back pain
  • 81% to 100%= Bed-bound or exaggerating symptoms
Baseline - End of the eighth week
Sahrmann Core Stability Test
Time Frame: Baseline - End of the eighth week
The Sahrmann core stability test is a 5-level test used to evaluate the ability of the core muscles to stabilize the spine. While the participant lying in a crook-supine position, the PBU will be inflated to 40 mmHg. Participants will perform the Sahrmann five-level test. A deviation of pressure more than 10 mmHg indicates that the stabilization action of stabilizer muscle has been lost.
Baseline - End of the eighth week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Mehmet Akif Güler, MSc/PT, Selcuk University / Faculty of Health Sciences / Department of Physiotherapy and Rehabilitation
  • Study Chair: Ertuğrul Demirdel, Asst. Prof, Ankara Yildirim Beyazit University / Faculty of Health Sciences / Department of Physiotherapy and Rehabilitation
  • Study Director: Ilknur Albayrak Gezer, Assoc. Prof, Selcuk University / Faculty of Medicine / Department of Physical Therapy and Rehabilitation
  • Study Director: Alaaddin Nayman, Assoc. Prof, Selcuk University / Faculty of Medicine / Department of Radiology
  • Study Director: Ezgi Akyıldız Tezcan, MD, Cumra Public Hospital / Department of Physical Therapy and Rehabilitation

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

March 1, 2022

Primary Completion (Anticipated)

September 1, 2022

Study Completion (Anticipated)

March 1, 2023

Study Registration Dates

First Submitted

March 21, 2022

First Submitted That Met QC Criteria

March 21, 2022

First Posted (Actual)

March 31, 2022

Study Record Updates

Last Update Posted (Actual)

March 31, 2022

Last Update Submitted That Met QC Criteria

March 21, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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