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临床试验/NCT03218644
NCT03218644已完成不适用

Effectiveness of a Propioceptive Exercise Program in Subjects With Inespecific Neck Pain

University of Valencia1 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2017年7月14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
47
试验地点
1
主要终点
Intensity of Pain

研究概览

简要总结

Introduction: Neck pain is among the most common and costly for industrialized societies. It is difficult to know the exact structure causing the pain so most are considered as non-specific neck pain. There is a correlation between the alteration of craneocervical proprioception and neck pain. The evidence for treatment with proprioceptive exercises is very limited.

Objective: To know the efficacy of a proprioceptive exercise program for neck pain and to compare its effects with a cervical mobility program.

Materials and Methods: Subjects between 18-65 years old with non-traumatic neck pain are included. They will be randomized into two groups of exercises: proprioception or mobility, which will be developed over a period of two weeks, every day, with a total of 10 sessions per patient.

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Neck pain (NAD I-II) of recent onset (0-3 months)

排除标准

  • •Cognitive difficulties
  • •Lack of commitment to attend sessions
  • •Subjects with pacemakers or defibrillators
  • •Being receiving another physiotherapeutic treatment
  • •Other pathologies

研究组 & 干预措施

Control group

Active Comparator

Follow the usual treatment and perform the exercises of cervical mobility before a mirror.

干预措施: Mobility exercises (Other)

Experimental group

Experimental

The same procedure is followed by substituting proprioceptive exercises for craniocervical sensorimotor control with a laser instrument located on the patient's head and a target.

干预措施: Proprioception exercises (Other)

结局指标

主要结局

Intensity of Pain

时间窗: four weeks

Visual Analogue Scale (VAS) was used to register the pain. The VAS is a 10-point rating scale.

次要结局

  • Pain points(four weeks)
  • Head Repositioning Test(four weeks)
  • Cervical movement range (CROM)(four weeks)
  • Neck Disability(four weeks)
  • Health status(four weeks)

研究者

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

GEMMA V ESPÍ LÓPEZ, PhD

Principal Investigator

University of Valencia

研究点 (1)

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