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临床试验/NCT03776019
NCT03776019已完成不适用

Efficacy of Audio-Visual-Perception-Enhancement (AVWF®) Method in Chronic Pain Patients

Klinikum Klagenfurt am Wörthersee2 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2019年2月15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
57
试验地点
2
主要终点
Change in Numeric Rating Scale of Pain Severity

研究概览

简要总结

It is anticipated that Audio-Visual-Perception-Enhancement (AVWF®) method leads to pain reduction and a decrease of inflammatory markers in chronic pain patients. Also an improvement of quality of life, self-perceived disability and depression in chronic pain patients is expected.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • chronic low back pain with a numeric rating scale of pain >= 4 for > 6 month
  • patients >18 years

排除标准

  • psychosis
  • drug addiction
  • pension process
  • pregnant women

结局指标

主要结局

Change in Numeric Rating Scale of Pain Severity

时间窗: Change from baseline Numeric Rating Scale of Pain Severity after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention

Validated 11 pt scale 0-10, to evaluate a patient's current severity of pain. A rating of 0 indicates no pain while 10 indicates the worst pain imaginable. A score of 4 or above is considered a clinically significant pain Level.

次要结局

  • Depression Anxiety Stress Scales(Change from baseline Depression Anxiety Stress Scales after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)
  • Hospital Anxiety and Depression Scale(Change from baseline Hospital Anxiety and Depression Scale after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)
  • Health related quality of life(Change from baseline health related quality of life after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)
  • Pittsburgh Sleep Quality Index(Change from baseline Pittsburgh Sleep Quality Index after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)
  • Pain Disability Index(Change from baseline Pain Disability Index after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)
  • Salival Cortisol level(Change from baseline salival cortisol level after 10 interventions, 4 weeks after the last intervention, and 3 month after the last intervention)

研究者

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

Rudolf Likar

Prim.Univ.Prof.Dr.

Klinikum Klagenfurt am Wörthersee

研究点 (2)

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