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临床试验/NCT02527252
NCT02527252已完成1 期

Benefits of Craniosacral Therapy in Patients With Chronic Low Back Pain: A Randomized Controlled Trial

Universidad de Almeria1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2015年7月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
64
试验地点
1
主要终点
Roland-Morris Disability Questionnaire (RMQ)

研究概览

简要总结

The purpose of the current randomized clinical trial was to analyze the effectiveness of craniosacral therapy on disability, pain intensity, kinesiophobia, quality of life, isometric endurance of trunk flexor muscles, mobility, and oxygen saturation, blood pressure, cardiac index, and biochemical estimation of interstitial fluid in individuals with chronic low back pain.

详细描述

Objective

To analyze the effects of craniosacral therapy on disability, pain intensity, quality of life, and mobility in patients with chronic low back pain.

Design: A single blinded randomized controlled trial. Setting: Clinical setting. Subjects: Sixty-four patients (42 females) with chronic low back pain. Interventions: Patients were randomly assigned to an experimental group (craniosacral therapy group) or a control group (classic massage group).

Main measures: Self-reported disability (Roland Morris Disability Questionnaire - primary outcome; and Oswestry Disability Index), pain intensity (a 10-point Numerical Pain Rating Scale), scale of kinesiophobia (Tampa Scale of Kinesiophobia), isometric endurance of trunk flexor muscles (McQuade Test), lumbar mobility in flexion, and oxygen saturation, blood pressure, cardiac index, and biochemical estimation of interstitial fluid.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •LBP for/over three months.
  • •age between 18 and 65 years.
  • •score equal or superior of four points on the Roland Morris Disability Questionnaire.
  • •not currently receiving physical therapy.

排除标准

  • •presence of lumbar stenosis
  • •diagnosis of spondylolisthesis
  • •diagnosis of fibromyalgia
  • •treatment with corticosteroid or oral medication within the past two weeks
  • •a history of spinal surgery
  • •disease of the central or peripheral nervous system

研究组 & 干预措施

Craniosacral therapy

Experimental

All treatments were applied by two experienced therapists with a 10-year certification in manipulative therapy after completion of their physical therapy degree and more than 20 years of clinical experience with patients. All patients received the intervention on the day of their initial examination. The techniques took 50 minutes and were conducted as follows:

  • Pelvic Diaphragm Release.
  • Respiratory Diaphragm Release.
  • Thoracic Inlet Release.
  • Hyoid release.
  • Sacral technique for stabilize L5/sacrum.
  • CV-4 Still Point Induction.

干预措施: Craniosacral therapy (Other)

Classic Massage

Active Comparator

Classics massage protocol was compounded by the following techniques of soft tissues massage: effleurage, petrissage, friction, and kneading. The techniques took thirty minutes.

干预措施: Classic Massage (Other)

结局指标

主要结局

Roland-Morris Disability Questionnaire (RMQ)

时间窗: Changes in 10 weeks and 14 weeks

It is one of the most used questionnaires for assessing disability due to LBP. This is a self-reported questionnaire consisting of 24 items reflecting limitations in different activities of daily living attributed to LBP including walking, bending over, sitting, lying down, dressing, sleeping, self-care and daily activities.

次要结局

  • Oswestry Low Back Pain Disability Index (ODI).(10 weeks and 14 weeks)
  • 10-point Numerical Pain Rating Scale(10 weeks and 14 weeks)
  • Tampa Scale of Kinesiophobia (TSK)(10 weeks and 14 weeks)
  • Isometric endurance of trunk flexor muscles(10 weeks and 14 weeks)
  • Lumbar mobility in flexion(10 weeks and 14 weeks)
  • Hemoglobin Oxygen Saturation(10 weeks and 14 weeks)
  • Systolic Blood Pressure(10 weeks and 14 weeks)
  • Diastolic Blood Pressure(10 weeks and 14 weeks)
  • Hemodynamic (Cardiac Index)(10 weeks and 14 weeks)
  • Insterticial Liquid Biochemical Estimation(10 weeks and 14 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adelaida María Castro-Sánchez

Dr

Universidad de Almeria

研究点 (1)

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