跳至主要内容
临床试验/NCT03469024
NCT03469024已完成不适用

Comparison of Effectiveness of a Home Rehabilitation Program vs an e-Healt Program on Disability, Pain, Fear of Movement, Quality of Life and Spinal Mobility in Patients With Chronic Low Back Pain.

Universidad de Almeria1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
1
主要终点
Change from baseline in Roland Morris Disability Questionnaire (RMDQ).

研究概览

简要总结

The main objetive of this study is to analyze the effectiveness of a home rehabilitaton program vs a e-Health program. Therapeutic approach will be by electroanalgesia and exercise of patients with chronic low back pain.

详细描述

A double blind clinical trial will be developed in a sample of 80 subjects with chronic low back pain. Patients will receive 3 weekly sessions of electroanalgesia and an exercise program for 8 weeks, for a total of 24 sessions. The aim is to analyze the effectiveness of a home rehabilitation program vs a web platform program on disability, pain, fear of movement, quality of life, resistance of the trunk flexors, lumbar mobility in flexion and muscular electrical activity.

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 (Investigator, Outcomes Assessor)

入排标准

年龄范围
30 Years 至 67 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Low back pain ≥ 3 months.
  • •Age between 30 and 67 years old.
  • •Score ≥ 4 points on the Roland Morris Disability Questionnaire.
  • •Not being receiving physical therapy.

排除标准

  • •Presence of lumbar stenosis.
  • •Diagnosis of spondylolisthesis.
  • •Diagnosis of fibromyalgia.
  • •Treatment with corticosteroids or oral medication in recent weeks.
  • •History of spine surgery.
  • •Contraindication of analgesic electrical therapy.
  • •Have previously received a treatment of electrical analgesia or exercise.
  • •Central or peripheral nervous system disease.
  • •Agoraphobia

研究组 & 干预措施

Home rehabilitation program

Experimental

It consists in a home rehabilitation program. Patients will recieve electroanalgesia with TENS and an exercise program following the McKenzie method. At first and second sessions, patients will be instructed on how to use electroanalgesia and how to perform the exercises. Then, patients will perform the therapy at home. Patients will perform the treatment 3 times per week, for 4 weeks, with a total of 24 sessions

干预措施: Home Rehabilitation Program (Other)

e-Health program

Active Comparator

It consists in a support system for the treatment of chronic low back pain based on web technologies. The system can register a subject and provide a treatment of electroanalgesia and exercise through the Mckenzie method. Video applications of electroanalgesia and exercises will be shown to patients who use their computer or mobile device to access the platform through the Internet. The treatments will be recommended by the system based on the database that is configured to accommodate the application of electroanalgesia and McKenzie exercises based on the diagnosis according to the McKenzie method.patients will perform the treatment 3 times per week, for 4 weeks, with a total of 24 sessions

干预措施: e-Health program (Other)

结局指标

主要结局

Change from baseline in Roland Morris Disability Questionnaire (RMDQ).

时间窗: At baseline, at 8 weeks and at 6 months

This is a self-reported questionnaire consisting in 24 items reflecting limitations in different activities of daily living attributed to low back pain including walking, vending over, sitting, lying down, dressing, sleeping, self-care and daily activities.

次要结局

  • Changes from baseline in Lumbar electromyography.(At baseline, at 8 weeks and at 6 months)
  • Change from baselina in range of motion and lumbar segmental mobility(At baseline, at 8 weeks and at 6 months)
  • Change from baseline in pain intensity. Visual analogue scale.(At baseline, at 8 weeks and at 6 months)
  • Change from baseline in lumbar mobility flexion.(At baseline, at 8 weeks and at 6 months)
  • Change from baseline in disability. Oswestry Low Back Pain Disability Idex.(At baseline, at 8 weeks and at 6 months.)
  • Change from baseline in Fear of Movement. Tampa Scale of kinesiophobia.(At baseline, at 8 weeks and at 6 months)
  • Change from Mcquade Test.(At baseline, at 8 weeks and at 6 months)
  • Change from baseline on Quality of Life. SF-36 Health questionnaire.(At baseline, at 8 weeks and at 6 months)

研究者

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

Adelaida María Castro-Sánchez

PhD

Universidad de Almeria

研究点 (1)

Loading locations...

相似试验