跳至主要内容
临床试验/NCT00901082
NCT00901082已完成不适用

The Effectiveness of Information and Relaxation on Pre-procedural Block Anxiety and Procedural Discomfort During Medial Branch Block: a Randomized Controlled Trial

Louise Lamb2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Change in the anxiety level prior to the nerve block as per the state trait anxiety questionnaire

研究概览

简要总结

Patient presenting to chronic pain clinics frequently undergo diagnostic and therapeutic spinal injections as part of their treatment. These procedures can cause significant level of apprehension in patients, which can lead to increased procedural times, increased procedural pain and reluctance to continue with the treatment program. It appears that certain interventions could reduce the anxiety and catastrophization levels and modify pain perception during medical procedures. The investigators therefore sought to evaluate the effect of a single 30 minutes information session which includes relaxation training administered 5 to 6 days before the nerve block procedure on patient's anxiety and catastrophization levels prior to the procedure and pain scores during the procedure, as well as the overall level of satisfaction with care received.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Care Provider)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patient scheduled to have a medial branch block
  • over 18 years of age

排除标准

  • adult able to give their own consent
  • patients who had a previous nerve block
  • patients who have a major psychiatric illness
  • patients who do not understand English or French

结局指标

主要结局

Change in the anxiety level prior to the nerve block as per the state trait anxiety questionnaire

时间窗: 5-7 days (Second visit and Day of block)

次要结局

  • Ease of performing the nerve block(Day of block)
  • Perceived pain as measured by NRS (numerical rating scale)(Throughout the study (Baseline, day of block and 1 month after))
  • Satisfaction level of the overall experience(Day after the block)
  • Unchanged catastrophization level(Baseline and day of block)

研究者

发起方
Louise Lamb
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Louise Lamb

Nurse

McGill University Health Centre/Research Institute of the McGill University Health Centre

研究点 (2)

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