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临床试验/NCT00151554
NCT00151554已完成不适用

Reducing ICU Related Anxiety Through a Structured Information Program. A Randomized Controlled Clinical Trial

Philipps University Marburg Medical Center1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2005年2月1日最近更新:
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
140
试验地点
1
主要终点
Patient self-reported anxiety

研究概览

简要总结

According to current evidence and psychological theorizing, the provision of information seems to be a promising way to reduce the anxiety of patients that is related to their scheduled ICU stay. An ICU-specific information program will be investigated in a randomized controlled clinical trial involving 120 patients undergoing elective open heart surgery and 20 patients undergoing abdominal surgery. It is expected that the patients in the test group will experience less anxiety and ICU related discomfort than patients in the control group.

详细描述

Objective

According to current evidence and psychological theorizing the provision of information seems to be a promising way to reduce anxiety of patients. In the case of surgical patients, admission to the intensive care unit (ICU) is strongly associated with uncertainty, unpredictability and anxiety for the patient. Thus, ICU-specific information could have a high clinical impact. For this reason this study will evaluate the efficacy of an ICU-specific information program for patients who undergo elective cardiac, abdominal or thoracic surgery and are scheduled for ICU stay.

Methods: The trial is designed as a prospective randomized controlled trial including an intervention and a control group. The control group receives the standard preparation currently conducted by surgeons and anesthesists. The intervention group additionally receives a standardized information program with specific procedural, sensory and coping information about the ICU. In addition the moderating effect of certain personality characteristics (need for cognition, high trait anxiety) will be investigated to identify groups of patients who benefit most from the information program.

Expected Results: A clinically relevant difference in anxiety and unpleasant experiences related to the ICU is expected after discharge from the ICU. Power calculation (alpha = 0.05; beta = 0.20; delta = 8.50 score points) resulted in a required sample size of N = 120 cardiac surgical patients (n = 60 vs. n = 60). Furthermore, N = 20 abdominal or thoracic surgical patients will be recruited (n = 10 vs. n = 10).

Conclusion: The proposed study promises to strengthen evidence on the effects of a specific, concise information program and thus should contribute to evidence based nursing (EBN).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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
否

入选标准

  • •Elective open heart or abdominal surgery including scheduled ICU stay
  • •Informed consent

排除标准

  • •Elective surgery without ICU stay
  • •Informed consent denied

研究组 & 干预措施

Control group

No Intervention

Intervention group

Experimental

干预措施: ICU-specific information program (Behavioral)

结局指标

主要结局

Patient self-reported anxiety

时间窗: after admission on standard ward

ICU related discomfort

时间窗: after admission on standard ward

次要结局

  • Objective health status parameters(postoperative phase of hospital stay)
  • Overall satisfaction with care(3 months after discharge)
  • Quality of life(3 months after discharge)

研究者

申办方类型
Other

研究点 (1)

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