Innovative Tool to Limit Spread of COVID 19 in Residential Aged Care Facilities
2021年3月4日 更新者：The University of Queensland
Innovative Tool to Limit Spread of COVID 19 in Residential Aged Care
This project is a randomised trial in order to determine if "gamification" can result in behaviour change for healthcare workers in the residential aged care setting.
The app is for Age Care and care workers at the front line who are working to protect those most vulnerable to COVID-19.
There are 2 groups in this trial on group will receive current and accurate information from an app.
The other group will receives the app with the addition of a gamification competent, this will include rewarding experiences for staff doing safety behaviours and wellbeing behaviours.
The purpose of the gamification is to create a calming and reassuring experience that injects positivity and joy where possible during this stressful time.
研究概览
详细说明
The study design will be a multi- centre cluster randomised control trial, where Age Care facilities are randomised into two groups:
- Newsfeed- gets the app with newsfeed only
- Gamification group- gets the full gamified app, including the newsfeed Workers in our network of residential aged care facilities will be invited to participate in a study of communication of information regarding COVID-19 and how they will play a role in preventing its spread.
研究类型
介入性
注册 (实际的)
34
阶段
- 不适用
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 90年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Age Health Care Worker
Exclusion Criteria:
-
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：预防
- 分配：随机化
- 介入模型：顺序分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：Newsfeed
This will provide you with reliable accurate information on the pandemic.
|
This will provide the user with reliable accurate information on the pandemic.
|
|
实验性的：Gamification
The gamification function will allow users to earn points for actions completed.
The gamification function has links to resources for infection control, watching or completing tasks or playing games to earn points.
Points can be viewed at a facility level, state level or national level.
|
This will provide the user with the newsfeed function and the addition of a gamification function
|
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 |
|---|---|---|
|
To compare the hours of sick leave used over the course of the 4-week period post randomisation for each group
大体时间：4 weeks
|
Compare the number of sick leave prior to users utilising the app and at the end of the 4 weeks between the arms
|
4 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
To compare handwashing behaviour
大体时间：4 weeks
|
Compare the amount of soap/sanitiser used between the arms
|
4 weeks
|
|
To compare self-testing rates
大体时间：4 weeks
|
Compare the number of self tests between the two arms
|
4 weeks
|
|
To compare the level of surface wipe down
大体时间：4 weeks
|
Compare the amount of wipes/disinfectant used between the two arms
|
4 weeks
|
|
To compare number of COVID-19 tests completed in Facilities
大体时间：4 weeks
|
Compare the number of COVID-19 tests between the two arms
|
4 weeks
|
|
To compare the number of COVID 19 infections in facilities
大体时间：4 weeks
|
Compare the number of COVID-19 infections between the arms
|
4 weeks
|
|
To compare the other types of outbreaks (Flu, gastroenteritis)
大体时间：4 weeks
|
Compare the number of flu and gastroenteritis outbreaks between the arms
|
4 weeks
|
|
To compare the awareness of COVID 19 training available to workers in the facilities
大体时间：4 weeks
|
Compare the COVID 19 training between the two arms, this is via a self reported survey
|
4 weeks
|
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To compare the awareness of PPE training available to workers in the facilities
大体时间：4 weeks
|
Compare the awareness of PPE training of the workers in the two arms, this is captured in self reported survey
|
4 weeks
|
|
To compare the levels of PPE material used in
大体时间：4 weeks
|
Compare the amount of PPE used between the arms
|
4 weeks
|
|
To compare the wellbeing and self-efficacy of the two groups
大体时间：4 weeks
|
Compare the wellbeing and self-efficacy between the two arms, this is captured in a self reported survey.
|
4 weeks
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：David L Paterson, PhD、The University of Queensland
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2020年5月6日
初级完成 (实际的)
2020年8月26日
研究完成 (实际的)
2020年8月26日
研究注册日期
首次提交
2020年5月4日
首先提交符合 QC 标准的
2020年5月4日
首次发布 (实际的)
2020年5月6日
研究记录更新
最后更新发布 (实际的)
2021年3月9日
上次提交的符合 QC 标准的更新
2021年3月4日
最后验证
2020年4月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.