The Effect of Nurse-led Video-assisted Discharge Training on Anxiety and Readiness for Discharge
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 89
- 试验地点
- 2
- 主要终点
- Anxiety
研究概览
简要总结
This clinical trial aims to evaluate the effect of nurse-led video-assisted discharge education on discharge readiness and anxiety in patients undergoing coronary artery bypass graft surgery.
The main questions that are aimed to be answered are:
Is there a difference between the discharge readiness levels of patients who received video-assisted discharge training and patients who received classical discharge training?
Is there a difference between the anxiety levels of patients receiving video-assisted discharge training and patients receiving classical discharge training?
Participants:
Experimental group Patients in the intervention group were administered the Readiness for Discharge scale and the State Anxiety Scale on the morning of discharge. Afterwards, the discharge training video prepared by the researchers was sent to their cell phones and they were allowed to watch it with the nurse. The researcher also encouraged the patients to ask questions when they did not understand a topic. Since the video remained on the patient's phone, they could watch it again after discharge. After the training, Discharge Readiness Scale and State Anxiety Scale were administered again.
Control group On the morning of discharge, patients in the control group were administered the Readiness for Discharge Scale and State Anxiety Inventory. The clinic nurse then gave discharge training, which is a clinical routine. After the training, the Readiness for Discharge Scale and State Anxiety Inventory were administered again.
详细描述
Type of Research This study is a quasi-experimental controlled design. Patients who underwent CABG surgery were divided into 2 groups as patients who received standard discharge training and patients who received video-assisted discharge training.
Place and Sample of the Study The study was conducted between January and October 2023 in a Thoracic-Cardiovascular Surgery Hospital in Istanbul. G*Power version 3.1 was used to calculate the sample size. According to the results of Weiss (2010), the sample size was calculated as 88, 44 intervention and 44 control, with an effect size of 0.32, a significance level (α) of 0.05, an expected power of 0.80, and an effect size estimate of 0.30. The study included 89 patients, 44 in the experimental and 45 in the control groups, who met the inclusion criteria. Inclusion criteria; over the age of 18, good mental health, speak Turkish, have no hearing or vision problems, have had first coronary artery bypass graft surgery.
Data Collection Tools Data were collected using Patient Information Form, Discharge Readiness Scale and State Anxiety Scale.
Patient Information Form: It was prepared by the researchers in line with the relevant literature. The form includes questions about age, gender, marital status, educational status, occupation, place of residence, income status, social security status, presence of an additional disease, smoking, with whom they live at home, presence of a caregiver at home, height, weight, date of hospitalisation, date of surgery, date of discharge.
Discharge Readiness Scale:
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 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
- •First coronary artery bypass graft surgeryi, good mental health, could speak Turkish
排除标准
- •had hearing or vision problem
结局指标
主要结局
Anxiety
时间窗: Postoperative 30 day
State anxiety scale score
Discharge readiness
时间窗: Postoperative 30 day
Discharge readiness scale score
次要结局
未报告次要终点
研究者
HATİCE DEMİRDAĞ
Phd
Uskudar University
