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临床试验/NCT06801145
NCT06801145已完成不适用

The Effect of Video-supported Education About the Intensive Care Process on Anxiety Levels and the ICU Experience of Patients Scheduled for Open-heart Surgery

Zeynep Turak1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2023年10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
发起方
Zeynep Turak
入组人数
110
试验地点
1
主要终点
Intensive care experience

研究概览

简要总结

This study was conducted to examine the effects of video-assisted education about the intensive care process on intensive care experiences and anxiety levels of patients scheduled for open-heart surgery.

Research Hypotheses H01: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does not affect their experiences of intensive care.

H1: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does affect their experiences of intensive care.

H02: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does not affect patients' anxiety levels.

H2: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does affect patients' anxiety levels.

详细描述

The study will include an experimental and a control group. Patients in the experimental group will be administered the Patient Introduction Form, Trait Anxiety and State Anxiety Scales 48 hours before surgery. Then, video-assisted training will be given about the intensive care process, and the state anxiety scale will be applied again 24 hours before the surgery. Twenty-four hours after discharge from the intensive care unit to the clinic, the State Anxiety Scale and Intensive Care Experience Scales will be applied again. These scales will also be applied to patients in the control group who did not receive video-assisted education. Control group patients will not receive any intervention other than standard nursing care.

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
None (Participant)

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

  • •Patients aged 18 and over,
  • •Cognitively competent,
  • •Communicative and cooperative,
  • •Patients undergoing planned surgery (patients not admitted for emergency surgery),
  • •Patients without a psychiatric diagnosis,
  • •Patients with sensory impairments such as vision, hearing, or speech,
  • •Patients with stable hemodynamic status in the clinic,
  • •Patients who volunteered to participate in the study were included in the study.

排除标准

  • •Patients who did not volunteer to participate,
  • •Patients whose surgery was canceled,
  • •Patients who underwent emergency surgery,
  • •Patients who underwent combined bypass and valve surgery,
  • •Patients with previous intensive care experience,
  • •Patients who developed complications before, during, or after surgery were excluded from the study.

研究组 & 干预措施

Experimental group

Experimental

Video training will be provided 48 hours before the surgery.

干预措施: Education with Video (Other)

Control group

No Intervention

This group will receive no intervention other than the applied scales; only standard nursing care will be maintained.

结局指标

主要结局

Intensive care experience

时间窗: 24 hours after arriving from intensive care care

Intensive care experience will be evaluated with the Intensive Care Experience Scale. The scale has been developed to evaluate the experiences of patients in the intensive care unit.10 of the scale questions evaluate the frequency of the emotional condition in which the patient live, while the other 9 evaluate the compliance of the patient to intensive care. The substances prepared to evaluate the harmony of the patient in intensive care; Scored between 1 and 5.

Anxiety level

时间窗: 48 hours before surgery, 24 hours before surgery, 24 hours after intensive care unit

Anxiety level will be evaluated with the State-Trait Anxiety Inventory.The State-Trait Anxiety Inventory was first developed by Spielberger and colleagues in 1971, and its Turkish adaptation was completed by Öner and Le Compte in 1985. The scale consists of a total of 40 items and two separate subscales. The first 20 items assess individuals' state anxiety levels, while the remaining 20 items assess trait anxiety levels.

次要结局

未报告次要终点

研究者

发起方
Zeynep Turak
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zeynep Turak

Master student

Ataturk University

研究点 (1)

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