Process Evaluation of a Residence-Based SARS-CoV-2 Testing Participation Pilot (RB-TPP)
2021年9月15日 更新者:Holly Blake、University of Nottingham
Mixed-methods Process Evaluation of a Residence-Based SARS-CoV-2 Testing Participation Pilot on a UK University Campus During the COVID-19 Pandemic.
Mixed-methods process evaluation of a residence-based asymptomatic SARS-CoV-2 testing participation pilot
研究概览
地位
完全的
条件
详细说明
Regular testing for SARS Coronavirus 2 (SARS-CoV-2) is an important strategy for controlling virus outbreaks on university campuses during the COVID-19 pandemic but testing participation rates can be low.
The Residence-Based Testing Participation Pilot (RB-TPP) was a novel intervention implemented at two student residences on a large university campus in the UK over four weeks.
The aim of the pilot was to increase the frequency of asymptomatic SARS-CoV-2 saliva testing onsite.
This process evaluation aimed to determine whether RB-TPP was implemented as planned and identify implementation barriers and facilitators.
A mixed-methods process evaluation was conducted alongside the RB-TPP.
Evaluation participants were students (who opted in, or out of the RB-TPP) and staff with a role in service provision or student support.
Monitoring data were collected from the intervention delivery team and meeting records.
Data were collected from students via an online survey (n=152) and seven focus groups (n=30), and from staff via individual interviews (n=13).
Quantitative data were analysed descriptively and qualitative data thematically.
研究类型
介入性
注册 (实际的)
152
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
-
Nottingham、英国、NG7 2HA
- University of Nottingham
-
-
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
- 孩子
- 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:
- Student is living in one of the two participating halls of residence.
- staff with operational or student support role.
- consents to participate.
Exclusion Criteria:
- Student is not living in the hall of residence at the start of the RB-TPP.
- does not consent to participate.
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:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Residence-based asymptomatic SARS-CoV-2 testing
The aim of the RB-TPP was to increase and maintain participation of students in regular COVID-19 testing in university residences.
The R-TPP was delivered over 4 weeks in April-May 2021 and required asymptomatic students to take a saliva test for COVID-19, twice weekly for four weeks.
This was combined with relaxed social restrictions within the residence during the study period (i.e., removing the need for 2 metre distancing between students living in the same residence), surge testing and enhanced support for students who were required to self-isolate (i.e., welfare and financial support).
|
SARS-CoV-2 asymptomatic saliva testing (as available to all students at staff at the participating university) delivered with relaxed social distancing (behavioural element) in two halls of residence.
|
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 |
|---|---|---|
|
Reach
大体时间:1 week
|
Program reach was evaluated through the number of students recruited into the RB-TPP compared to the number of potentially eligible students living in one of the two participating sites in April 2021
|
1 week
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Adherence
大体时间:4 weeks
|
Participant adherence was defined as the proportion of students who completed all tests offered.
|
4 weeks
|
|
Dose
大体时间:4 weeks
|
Number of tests offered
|
4 weeks
|
|
Generalised Anxiety Disorders Scale (Spitzer et al., 2006; Kroenke et al., 2007).
大体时间:4 weeks
|
A 7-item anxiety scale with good reliability, as well as criterion, construct, factorial, and procedural validity.
A cut point of >=10 indicates moderate to severe anxiety.
Higher scores indicate higher anxiety.
|
4 weeks
|
|
Student Focus Groups
大体时间:4 weeks
|
Student's views towards the RB-TPP.
Small group discussions lasting approximately 60 mins conducted at mid-point and/or programme end.
|
4 weeks
|
|
Staff interviews
大体时间:4 weeks
|
Staff views towards the RB-TPP.
Individual interviews lasting approximately 20-60 mins conducted at programme end.
|
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:Holly Blake, PhD、University of Nottingham
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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)
2021年4月1日
初级完成 (实际的)
2021年7月31日
研究完成 (实际的)
2021年7月31日
研究注册日期
首次提交
2021年9月6日
首先提交符合 QC 标准的
2021年9月9日
首次发布 (实际的)
2021年9月16日
研究记录更新
最后更新发布 (实际的)
2021年9月22日
上次提交的符合 QC 标准的更新
2021年9月15日
最后验证
2021年9月1日
更多信息
与本研究相关的术语
其他研究编号
- FMHS 96-0920
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
IPD 计划说明
The datasets generated and/or analysed during the current study are not publicly available due to risk of identification of participants and service providers but are available from the corresponding author on reasonable request.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.