Automated Check-in Data Collection Study
- Conditions
- Primary Care
- Registration Number
- NCT03798756
- Lead Sponsor
- Keele University
- Brief Summary
The aim of this study is to examine patient acceptability, for providing brief research information, whilst self-completing an automated check-in screen prior to any general practice consultation.
- Detailed Description
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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 9274
- 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.
• Patients under the age of 18 attending the general practice for a consultation with a healthcare professional.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Self-reported Bodily Pain Through study completion at 1st visit (Day 1) 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.
- Secondary Outcome Measures
Name Time Method Bodily Pain Response Through study completion at 1st visit (Day 1) Proportion of participants answering the bodily pain research question using an automated check-in screen.
Consent to Contact Response Through study completion at 1st visit (Day 1) Proportion of participants answering the consent to contact research question using an automated check-in screen.
Trial Locations
- Locations (1)
New Cross Hospital
🇬🇧Wolverhampton, United Kingdom