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Effects of Diaphragmatic and Iliopsoas Myofascial Release in Patients With Chronic Low Back Pain

Effects of Diaphragmatic and Iliopsoas Myofascial Release in Patients With Chronic Low Back Pain: A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04415021
Enrollment
42
Registered
2020-06-04
Start date
2020-02-01
Completion date
2021-01-06
Last updated
2022-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain, Recurrent

Keywords

Low Back Pain, Diaphragm, iliopsoas, Myofascial Release

Brief summary

The aim of this study is to effectively investigate the relaxation of the diaphragm and iliopsoas muscle with myofascial technique in patients with chronic low back pain.

Detailed description

Low back pain is a common health problem that can be seen as a symptom and symptom of many diseases in the clinic. Myofascial release technique is thought to be effective in patients with chronic low back pain. Therefore, when the literature is examined, it has been observed that the myofascial release technique has studies on pain, range of motion, functionality, muscle stiffness and shortness. This study will be performed on patients with a total of 42 low back pain. The cases will be divided into 2 groups of 21 people by simple random sampling. Group 1 (control) will be used with sham diaphragm and iliopsoas muscle myofascial release technique and traditional physiotherapy method. The second group (experiment) will apply the diaphragm and the myofascial release technique of the iliopsoas muscle and the traditional physiotherapy method. Patients will be treated for 4 weeks. Traditional physiotherapy method will be applied a total of 20 sessions 5 days a week. A total of 12 sessions will be performed, with the myofascial release technique of the diaphragm and iliopsoas muscle applied 3 days a week. The study focuses on the analysis of the following variables: Pain : Numerical Pain Scale Joint Range of Motion: Goniometer Flexibility: Tape Measure Pulmonary Function Test: Spirometer Anxiety and Depression: Beck Depression inventory Kinesiophobia: Tampa Kinesiophobia Scale Disability: Roland-Morris Disability Questionnaire The results of these pre-intervention and post-intervention variables will be compared between the two groups .

Interventions

OTHERExperimental: Diaphragmatic and İliopsoas Myofascial Release Techniques

Subjects in this arm will receive different myofascial release techniques aimed to relaxation the myofascial tension of the diaphragmatic and iliopsoas muscles.

OTHERSham Comparator: Sham Myofascial Release Techniques

Subjects in this arm will receive the same manual techniques of the diaphragmatic and iliopsoas myofascial release group, but without the myofascial stimulus.

Sponsors

Istanbul Medipol University Hospital
CollaboratorOTHER
Ümit SIĞLAN
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with chronic low back pain diagnosed by the physician between the ages of 20-50 * Both genders * People who have low back pain for 3 months or more * Persons who have not received physical therapy application for the past 6 months, who have not used analgesics and non-streoids * Volunteer patients

Exclusion criteria

* Having had surgery for the lumbar region or had a surgical diagnosis * Spondylolisthesis and inflammatory symptoms in the spine * Pregnant patients * Other contraindicated conditions determined by the physician: 1. Those with systemic infections 2. Those with undiagnosed breathing difficulties 3. Those with undiagnosed bowel and bladder problems

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in range of motin on goniometer at 4 weeksBaseline and 4 weeksThe goniometer is an instrument which measures the available range of motion at a joint. If a patient or client is suffering from decreased range of motion in a particular joint, the therapist can use a goniometer to assess what the range of motion is at the initial assessment, and then make sure the intervention is working by using the goniometer in subsequent sessions.
Change from baseline in flexibility on tape measure at 4 weeksBaseline and 4 weeksTape Measure. This test is used to assess the degree of flexibility of the lumbal region.
Change from baseline in pulmonary function test on the spirometer at 4 weeksBaseline and 4 weeksSpirometer. A spirometer is the main piece of equipment used for basic Pulmonary Function Tests (PFTs). Lung diseases such as asthma, bronchitis, and emphysema can be ruled out from the tests. In addition, a spirometer is often used for finding the cause of shortness of breath, assessing the effect of contaminants on lung function, the effect of medication, and evaluating progress for disease treatment
Change from baseline in pain on the Numeric Rating Scale at 4 weeksBaseline and 4 weeksThe Numeric Rating Scale. This scale is an 11-point scale for patient self-reporting of pain. It is based solely on the ability to perform activities of daily living (ADLs) and can be used for adults and children 10 years old or older.

Secondary

MeasureTime frameDescription
Change from baseline in kinesiophobia on the Tampa Scale of Kinesiophobia at 4 weeksBaseline and 4 weeksTampa Scale of Kinesiophobia .This scale is used to assess the patients' fear of pain or re-injury due to movement. It consists of 17 items and assesses various factors of fear/avoidance and injury/re-injury in several activities. Total score of the scale varies between 17 and 68 and higher scores represent higher levels of kinesiophobia.
Change from baseline in disability on the Roland-Morris Disability Questionnaire at 4 weeksBaseline and 4 weeksThe Roland-Morris Disability Questionnaire. This questionnaire is a self-administered disability measure in which greater levels of disability are reflected by higher numbers on a 24-point scale. The Roland-Morris Disability Questionnaire has been shown to yield reliable measurements, which are valid for inferring the level of disability, and to be sensitive to change over time for groups of patients with low back pain.
Change from baseline in anxiety and depression on the Beck Depression Inventory at 4 weeks .Baseline and 4 weeksThe Beck Depression Inventory.This inventory is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026