Automated Check-in Data Collection Study (ACDC)
研究概览
地位
条件
详细说明
The Automated Check-in Data Collection (AC DC) Study, is a pilot feasibility study, observing patients consulting in general practice and completing an automated check-in screen prior to their booked appointment, to confirm their attendance. Participants will be recruited over three weeks from approximately 11 participating general practices.
The primary objective of the study is to assess patient acceptability for answering brief research questions in the general practice waiting room, using an automated check-in screen. This will be measured by observing the percentage of completed automated check-in screens with entered research data.
Secondary objectives will assess check-in completion of self-reported pain and willingness to be contacted about future research studies of relevance. Reported severity of bodily pain experienced over the last 4 weeks and the proportion of patients agreeing to be contacted about future research studies of relevance, will be observed.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Wolverhampton、英国、WV10 0QP
- New Cross Hospital
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Patients 18 years of age or over attending participating general practices for a consultation with any healthcare professional.
- Patients registered with the participating general practice during the specified recruitment period.
- Patients able to read and respond in English.
Exclusion Criteria:
• Patients under the age of 18 attending the general practice for a consultation with a healthcare professional.
学习计划
研究是如何设计的？
设计细节
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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Self-reported Bodily Pain
大体时间：Through study completion at 1st visit (Day 1)
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To assess what self-reported degrees of pain were reported by participants and what proportion of participants did answer a research question within the general practice waiting room using an automated check-in screen.
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Through study completion at 1st visit (Day 1)
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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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Bodily Pain Response
大体时间：Through study completion at 1st visit (Day 1)
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Proportion of participants answering the bodily pain research question using an automated check-in screen.
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Through study completion at 1st visit (Day 1)
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Consent to Contact Response
大体时间：Through study completion at 1st visit (Day 1)
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Proportion of participants answering the consent to contact research question using an automated check-in screen.
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Through study completion at 1st visit (Day 1)
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合作者和调查者
调查人员
- 研究主任：Christian D Mallen、University of Keele
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
其他研究编号
- RG-0275-18 V1.0
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
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.
初级卫生保健的临床试验
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