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临床试验/NCT07222839
NCT07222839Enrolling By Invitation不适用

Exploring the Effect of Visually Immersive Video Education on Cardiothoracic Surgery Patients' Preoperative Anxiety and Postoperative Outcomes

Baptist Health South Florida1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2026年1月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
200
试验地点
1
主要终点
Anxiety relief (self-report measure 2 - Visual Analog Scale for Anxiety)

研究概览

简要总结

The purpose of this quasi-experimental study is to examine the effect of visually immersive preoperative education on levels of anxiety and patient outcomes in patients undergoing cardiothoracic (open heart) surgery

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
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

  • •Inpatients and outpatients scheduled for elective cardiothoracic (open heart) surgery

排除标准

  • •Patients undergoing emergent cardiothoracic (open heart) surgery
  • •Patients with altered mental status
  • •History of mental health disorders (schizophrenia and bipolar disorder)
  • •Legally blind/complete blindness and hearing impaired (without hearing aids)

研究组 & 干预措施

Intervention - Visually Immersive Video Education

Experimental

Participants receive visually immersive (virtual reality-designed) preoperative video education shown on a tablet that orients patients to the postoperative CVICU environment, equipment, and expected recovery processes. After viewing the video, the open-heart trained CVICU nurse provides opportunity for discussion, clarification, and questions. Assignment to this arm occurs during intervention weeks (Weeks 1-2 of each month, per protocol).

干预措施: Visually Immersive Video (Behavioral)

Control - Standard Preoperative Education

Active Comparator

Participants receive standard preoperative education consisting of a basic verbal explanation of what to expect postoperatively on arrival to the CVICU, followed by opportunity for questions. Assignment to this arm occurs during control weeks (Weeks 3-4 of each month, per protocol).

干预措施: Standard of Care (Behavioral)

结局指标

主要结局

Anxiety relief (self-report measure 2 - Visual Analog Scale for Anxiety)

时间窗: 30 minutes

Patient's anxiety will be measured using the Visual Analog Scale for Anxiety (VAS-A), a slider scale of 0 - 100 is used to self-report anxiety (0 = not anxious and 100 = extremely anxious), taken before and after preoperative education is received.

Anxiety relief (self-report measure 1 - State-Trait Anxiety Inventory)

时间窗: 30 minutes

Patient's anxiety will be measured using the 20-item State-Trait Anxiety Inventory (STAI) (state scale only) (higher scores indicate higher anxiety), taken before and after preoperative education is received.

次要结局

  • Anxiety relief (physiological measure 1 - blood pressure)(30 minutes)
  • Anxiety relief (physiological measure 2 - heart rate)(30 minutes)
  • Anxiety relief (physiological measure 3 - respiratory rate)(30 minutes)
  • Postoperative CVICU Outcome 1 - Length of Stay(Within 30 days after the patient is discharged from CVICU)
  • Postoperative CVICU Outcome 2 - Intubation Time(Within 30 days after the patient is discharged from CVICU)
  • Postoperative CVICU Outcome 3 - Re-intubation(Within 30 days after the patient is discharged from CVICU)
  • Postoperative CVICU Outcome 4 - Blood Sugar Regulation(Within 30 days after the patient is discharged from CVICU)

研究者

发起方
Baptist Health South Florida
申办方类型
Other
责任方
Sponsor

研究点 (1)

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