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临床试验/NCT02222051
NCT02222051已完成不适用

Tai Chi for Chronic Non-specific Neck Pain: A Randomized Controlled Trial

Universität Duisburg-Essen2 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2014年8月最近更新:
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
114
试验地点
2
主要终点
pain intensity

研究概览

简要总结

In this study the efficacy of Tai Chi will be tested in comparison to conventional neck exercises and usual care in a randomized controlled trial. Tai Chi and neck exercises will be lead by a trained exercise therapist and Tai Chi instructor, both groups receive 12 weeks of training, once weekly for 60-90 min in a group setting. Pain, Disability, quality of life, wellbeing, stress perception, psychological distress will be used to determine effects.

详细描述

see above

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • chronic non specific neck pain (3 months at least)
  • 45mm pain intensity on average on the visual analog scale

排除标准

  • specific neck pain due to
  • inflammatory diseases
  • rheumatic diseases
  • neurological diseases
  • prolapse or protrusion
  • oncological disease
  • trauma (whiplash)
  • congenital deformity of the spine
  • severe comorbidity (somatic, psychiatric)
  • pregnancy
  • participation in other clinical trials
  • regular practice of tai chi, qigong, yoga in the past 6 months
  • medication with opioids

研究组 & 干预措施

Tai Chi

Experimental

Simplified 24 Yang Style 12 weeks, 1x/week, 60-90 minutes

干预措施: Tai Chi (Behavioral)

Neck exercise

Active Comparator

conventional neck exercises 12 weeks, 1x/week, 60 min stretching and strengthening, neck education

干预措施: Neck exercises (Behavioral)

Usual care

No Intervention

Usual care, no specific study intervention this group is offered Tai Chi or neck exercises at the end of the study

结局指标

主要结局

pain intensity

时间窗: week 12

pain intensity on a visual analogue scale (0-100mm)

次要结局

  • pain intensity(week 24)
  • pain on movement(week 12, week 24)
  • neck disability(week 12, week 24)
  • health related quality of life(week 12, week 24)
  • Anxiety and Depression(week 12, week 24)
  • Wellbeing(week 12, week 24)
  • Stress(week 12, week 24)
  • interoceptive awareness(week 12, week 24)
  • Postural Awareness(week 12, week 24)
  • Safety(week 24)
  • pain intensity ratings(week 12)
  • use of analgetics(week 12)
  • use of concomitant therapies(week 12)

研究者

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

Romy Lauche

PhD

Universität Duisburg-Essen

研究点 (2)

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