Effects of Virtual Reality After Liver Transplantation (VR-LT)
Effects of Virtual Reality on Pain, Fatigue and Vital Signs After Liver Transplantation A Randomized Controlled Trial
This randomized controlled study aims to evaluate the effects of a virtual reality intervention on pain, fatigue and vital signs in patients during the early postoperative period after liver transplantation. Postoperative symptoms such as pain and fatigue may negatively affect recovery and patient comfort. Virtual reality has emerged as a non-pharmacological method that may help reduce these symptoms by providing distraction and relaxation.
A total of 84 patients were randomly assigned to an experimental group or a control group. The experimental group received a 20-minute virtual reality session, while the control group received standard care. Pain, fatigue and vital signs were measured before and after the intervention.
This study aims to determine whether virtual reality can improve patient comfort and physiological stability and support recovery after liver transplantation.
研究概览
详细说明
This study was designed as a prospective, randomized controlled, single-blind trial to evaluate the effects of a virtual reality intervention on pain, fatigue, and vital signs in patients during the early postoperative period after liver transplantation.
Liver transplantation is a life-saving procedure; however, patients frequently experience postoperative symptoms such as pain and fatigue, which may negatively affect recovery, physiological stability, and overall patient comfort. Non-pharmacological interventions have gained increasing attention in recent years as supportive approaches to improve postoperative outcomes. Virtual reality is an emerging technology that provides immersive distraction and relaxation, potentially reducing symptom perception and enhancing patient well-being.
The study was conducted in the organ transplantation clinic of a university hospital between May 2025 and January 2026. A total of 84 patients who met the inclusion criteria were randomly assigned to either the experimental group (n=42) or the control group (n=42) using a computer-based randomization method.
Patients in the experimental group received a 20-minute virtual reality intervention during the early postoperative period, while patients in the control group received standard care without additional intervention. Pain levels were assessed using the Numerical Rating Scale (NRS), fatigue levels were measured using the Brief Fatigue Inventory (BFI), and vital signs including heart rate, respiratory rate, and blood pressure were recorded. All measurements were obtained before the intervention and 15 minutes after the intervention.
The primary objective of the study was to determine the effect of virtual reality on fatigue levels. Secondary outcomes included pain and vital signs. Data were analysed using appropriate statistical methods, and statistical significance was set at p<0.05.
This study aims to contribute to the evidence base regarding the effectiveness of virtual reality as a non-pharmacological nursing intervention and to support its integration into clinical practice to improve postoperative care in liver transplantation patients.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Malatya、土耳其(türkiye)
- Inonu University Liver Transplantation Institute
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Age ≥18 years
- Underwent liver transplantation
- In the early postoperative period
- Able to communicate verbally
- No diagnosed psychiatric disorder
- Hemodynamically stable
- Pain score ≥4 on the Numerical Rating Scale (NRS)
- Willing to participate in the study
Exclusion Criteria:
- Presence of severe postoperative complications
- Cognitive impairment or inability to understand instructions
- Visual or hearing impairments preventing use of virtual reality
- History of motion sickness or vertigo related to virtual reality use
- Chronic diseases that may affect fatigue or vital signs (e.g., uncontrolled cardiovascular or respiratory diseases)
- Refusal to participate
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Experimental Group
Participants received a 20 minute virtual reality intervention during the early postoperative period following liver transplantation.
The intervention was administered using a head mounted display and aimed to reduce fatigue and improve physiological parameters
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A 20 minute immersive virtual reality session was administered using a headmounted display during the early postoperative period following liver transplantation.
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有源比较器:Control Group
Participants received routine postoperative care without any additional intervention
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Participants received routine postoperative care without any additional intervention
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in fatigue severity
大体时间:Baseline and 15 minutes after intervention
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Change in fatigue severity measured using the Brief Fatigue Inventory (BFI) total score (range: 0-10; higher scores indicate greater fatigue)
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Baseline and 15 minutes after intervention
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in pain intensity
大体时间:Baseline and 15 minutes after intervention
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Measured using the Numerical Rating Scale (NRS) (range: 0-10; higher scores indicate greater pain)
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Baseline and 15 minutes after intervention
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Change in heart rate (beats per minute)
大体时间:Baseline and 15 minutes after intervention
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Change in heart rate measured in beats per minute (bpm).
Heart rate was recorded as part of routine vital sign monitoring to evaluate the physiological response to the virtual reality intervention.
Lower values may indicate improved relaxation and autonomic stability.
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Baseline and 15 minutes after intervention
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Change in systolic and diastolic blood pressure (mmHg)
大体时间:Baseline and 15 minutes after intervention
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Change in systolic and diastolic blood pressure measured in millimeters of mercury (mmHg).
Blood pressure was recorded as part of routine vital sign monitoring to evaluate the cardiovascular response to the virtual reality intervention.
Lower values may indicate improved physiological stability and relaxation.
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Baseline and 15 minutes after intervention
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Change in systolic and diastolic blood pressure (mmHg)
大体时间:Baseline and 15 minutes after intervention
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Change in systolic and diastolic blood pressure measured in millimeters of mercury (mmHg).
Blood pressure was assessed as part of routine vital sign monitoring to evaluate the cardiovascular response to the intervention.
Lower values may indicate improved physiological stability.
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Baseline and 15 minutes after intervention
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 25H04 (其他赠款/资助编号:Malatya Turgut Ozal University Scientific Research Projects Unit)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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