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

Low Back Pain, Recurrent Clinical Trial

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

Clinical Trial 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.

Clinical Trial 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 . ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04415021
Study type Interventional
Source Istanbul Medipol University Hospital
Contact
Status Completed
Phase N/A
Start date February 1, 2020
Completion date January 6, 2021
View Details
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