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临床试验/NCT05279794
NCT05279794已完成不适用

Efficacy of Two Types of Non-invasive Erector Spinae Muscle Taut Band Therapy in University Students With Low Back Pain: A Randomized Clinical Trial

Universidad Católica San Antonio de Murcia2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年3月21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
60
试验地点
2
主要终点
Pain intensity

研究概览

简要总结

Non-specific low back pain can be caused by the presence of active trigger points in the muscles of the lumbopelvic region. Trigger points are defined as hypersensitive points within a taut band of a musculoskeletal system that cause pain during contraction, stretching, or stimulation of said muscle. If these points are active, they can trigger referred pain, local tenderness, and vegetative responses. There is scientific evidence of the improvement of the treatment of these points through non-invasive manual techniques. The objective of this study will be to determine the effect of Strain Counterstrain and Myofascial Induction techniques in subjects with low back pain secondary to the presence of active trigger points in the lumbopelvic region. Hyperexcitable myofascial trigger points located within a taut band of skeletal muscle or fascia cause referred pain, local tenderness, and autonomic changes. The scientific data refer to an immediate improvement in the symptoms of these active points treated with manual therapy. Based on these factors, the objective of the study is to determine the effect of the combined therapy of the Strain Counterstrain technique and Myofascial Induction in participants with the presence of an active trigger point in the erector spinae muscle.

详细描述

The treatment will last a total of 15 minutes accompanied by a baseline assessment and after 10 minutes of the intervention in 2 experimental groups and a placebo group, of no-pain positioning. In addition to basic indices and scales of low back pain and disability caused by low back pain, it is intended to measure flexibility, range of motion, proprioception and cognition through software with sensors of the latest technology when representing reliable results in differences between techniques.

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 (Care Provider, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of low back pain
  • Presence of active trigger point in the erector spinae as described by Lawrence H. Jones

排除标准

  • Participants who present dizziness, vertigo;
  • Previous or scheduled surgeries in the lumbar spine and/or lower extremities;
  • Suspicion of serious fractures or pathologies (tumor, inflammation, infection, rheumatological disorder, systemic disease, presence of fever);
  • Diagnosis of radiculopathy or neuropathy;
  • Structural deformity in the spine; spondyloarthropathy, disabling pain and physical disability;
  • Use of pain relievers or anti-inflammatory drugs in the last 48 hours;
  • Neurological or psychiatric disorder;
  • Presence or suspicion of pregnancy

结局指标

主要结局

Pain intensity

时间窗: 20 minutes

Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10

Pression algometer

时间窗: 20 minutes

Measures pressure pain thresholds

次要结局

  • Countermovement jump test(20 minutes)
  • Spinal test(20 minutes)

研究者

发起方
Universidad Católica San Antonio de Murcia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan Martínez Fuentes

Study Director

Universidad Católica San Antonio de Murcia

研究点 (2)

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