Evaluating the Impact of Video Discharge Instructions for Mohs Surgery Post-Operative Care
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 14
- 试验地点
- 2
- 主要终点
- Ratio of patients in the intervention group who call the clinic compared to percentage of patients in the control group who call the clinic
研究概览
简要总结
The purpose of this research is to look at how educational videos provided by doctors might affect patients knowledge, satisfaction, confidence, and anxiety with post-operative Mohs surgery care. Patients will be randomized to either: 1) a group that receives educational videos in addition to standard-of-care written and verbal instructions or 2) a group that receives only standard-of-care written and verbal instructions.
详细描述
The Primary Objective of this study is to determine if video discharge instructions, when added to standard of care written and verbal instructions, lead to a decrease in unnecessary phone calls from patients in a Mohs dermatology clinic.
The Secondary Objectives of this study are to determine if video discharge instructions, when added to standard of care written and verbal instructions, help to improve patients' satisfaction with education materials provided by the clinic, improve patients' knowledge of post-operative management, improve patients' confidence in taking care of their suture site post-operatively, and reduce post-operative anxiety about their suture site.
This study will be a randomized controlled trial in which the impact of video discharge instructions on patient calls, anxiety, and confidence will be evaluated. Patients will be randomized using a permuted block model generated through SAS.
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
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 who underwent a linear closure on the face at UH Mohs clinic
- •Fluent English speakers
排除标准
- •● Non-fluent English speakers
结局指标
主要结局
Ratio of patients in the intervention group who call the clinic compared to percentage of patients in the control group who call the clinic
时间窗: Up to 8 weeks after discharge
Researchers will record when each participant calls the clinic. The number of people who call in the intervention group will be compared to the number of people who call in the control group. This will give an efficacy measure of the video discharge instructions
次要结局
- Difference in satisfaction in intervention group versus control group(Up to 8 weeks after discharge)
- Difference in self reported anxiety levels in intervention group versus control group(Up to 8 weeks after discharge)
- Difference in knowledge of discharge instructions in intervention group versus control group(Up to 8 weeks after discharge)
- Difference in confidence in intervention group versus control group(Up to 8 weeks after discharge)