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临床试验/NCT04014998
NCT04014998已完成不适用

Investigation of the Effectiveness of Virtual Reality Applications in Addition to Exercise Program in People With Chronic Neck Pain

Hacettepe University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年10月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Joint position sense error will assessed by Cervical Range of Motion device.

研究概览

简要总结

Virtual reality application has been increasing in recent years for pain control, distraction in wound care, treatment of anxiety disorders and support for physical rehabilitation. For example, it has been found to be effective in reducing pain when used in addition to medical treatment during bandaging of severe burns. The studies related with chronic pain patients were stated that virtual reality application was found to be interactive and fun by patients. Therefore, The aim of this study was to investigate the effects of virtual reality on pain threshold, disability, balance, proprioception, exercise sustainability, muscular performance in neck region, quality of life and anxiety / depression in addition to the exercise program that includes stabilization exercises in patients with chronic neck pain.

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
None

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

入选标准

  • to have pain more than 3 months,
  • to be sedentary,
  • to have Neck Disability Index score more than 10.

排除标准

  • to have neurological deficits, vestibular pathology, history of surgery.

结局指标

主要结局

Joint position sense error will assessed by Cervical Range of Motion device.

时间窗: Change from baseline joint position sense error (cervical flexion, extension, lateral flexions and rotations) after 6 weeks.

Joint position sense error will assessed by Cervical Range of Motion device.

Balance will assessed by Dynamic Posturography.

时间窗: Change from baseline sensorial organization test (vestibular, visual and proprioceptive components), limits of stability (reaction time, movement velocity, endpoint excursion, maximum excursion, directional control) and unilateral stance after 6 weeks.

Balance will assessed by Dynamic Posturography.

次要结局

  • Quality of life will assessed by Short-form 36.(Change from baseline quality of life after 6 weeks.)
  • cervical lordosis angle(Change from baseline cervical lordosis after 6 weeks.)
  • Disability will assessed by Profile Fitness Mapping Questionnaire(Turkish).(Change from baseline disability after 6 weeks.)
  • Kinesiophobia will assessed by Tampa kinesiophobia Scale(Change from baseline kinesiophobia after 6 weeks.)
  • Shoulder protraction and forward head posture were assessed by photography method.(Change from baseline shoulder protraction and forward head posture after 6 weeks.)
  • Pain threshold will assessed by algometer device.(Change from baseline pain threshold of both the right and left upper trapezius, the right and left articular pillar between cervical 1 and 2, the right and left cervical 5 and 6 after 6 weeks.)
  • muscle strength will assessed by dynamometer and biofeedback device(Change from baseline muscle strength after 6 weeks.)
  • Pain intensity will assessed with Visual Analog Scale.(Change from baseline pain intensity after 6 weeks.)
  • Anxiety-depression will assessed by Hospital Anxiety-depression scale.(Change from baseline anxiety-depression after 6 weeks.)

研究者

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

HATİCE ÇETİN

Research Assisstant

Hacettepe University

研究点 (1)

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