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临床试验/NCT04415021
NCT04415021已完成不适用

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

Ümit SIĞLAN1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2020年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
42
试验地点
1
主要终点
Change from baseline in flexibility on tape measure at 4 weeks

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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:
  • Those with systemic infections
  • Those with undiagnosed breathing difficulties
  • Those with undiagnosed bowel and bladder problems

结局指标

主要结局

Change from baseline in flexibility on tape measure at 4 weeks

时间窗: Baseline and 4 weeks

Tape 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 weeks

时间窗: Baseline and 4 weeks

Spirometer. 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 weeks

时间窗: Baseline and 4 weeks

The 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.

Change from baseline in range of motin on goniometer at 4 weeks

时间窗: Baseline and 4 weeks

The 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.

次要结局

  • Change from baseline in disability on the Roland-Morris Disability Questionnaire at 4 weeks(Baseline and 4 weeks)
  • Change from baseline in anxiety and depression on the Beck Depression Inventory at 4 weeks .(Baseline and 4 weeks)
  • Change from baseline in kinesiophobia on the Tampa Scale of Kinesiophobia at 4 weeks(Baseline and 4 weeks)

研究者

发起方
Ümit SIĞLAN
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ümit SIĞLAN

Principal Investigator

Istanbul Medipol University Hospital

研究点 (1)

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