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临床试验/NCT01982656
NCT01982656已完成不适用

Effects of Massage Technique for Pain, Anxiety, and Delirium Management in ICU Patients With Subarachnoid Hemorrhage

Sara E. Hocker, M.D2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年12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
发起方
入组人数
50
试验地点
2
主要终点
Change in Pain Score

研究概览

简要总结

This research study seeks to explore the effects of massage techniques on pain and anxiety relief among patients with subarachnoid hemorrhages in the ICU setting in comparison to subarachnoid hemorrhagic patients using standard medical therapy. In addition, our aim is to decrease the overall medication use to treat pain and anxiety, and to determine the impact of massage on sleep duration, quality, and breathing. Our goal is to improve and promote comfort during the ICU stay as well as decrease the need for narcotic medication usage.

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

  • Clinical diagnosis of aneurysmal subarachnoid hemorrhage

排除标准

  • Upper extremity deep vein thrombus
  • Active alcohol or drug withdrawal

研究组 & 干预措施

Massage technique

Experimental

In addition to standard medical care and pharmacologic interventions, massage technique for 20 minutes for 5 to 14 days while in the ICU will be provided to help alleviate pain and anxiety in the patient.

干预措施: Massage (Other)

No intervention

Placebo Comparator

Patients with an aneurysmal subarachnoid hemorrhage will receive standard medical care to include pharmacologic interventions prescribed by the primary physician and nonpharmacologic interventions provided by the bedside RN such as ice or heat to address their pain and anxiety needs.

干预措施: Massage (Other)

结局指标

主要结局

Change in Pain Score

时间窗: Baseline to 14 days

Over the course of the intervention period, the primary outcome of decrease in pain will be decreased as compared to the control group. This will be measured using the Pain Scale.

次要结局

  • Sleep quantity(5-14 days)

研究者

发起方
Sara E. Hocker, M.D
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Sara E. Hocker, M.D

Principle Investigator

Mayo Clinic

研究点 (2)

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