MedPath

Automated Check-in Data Collection Study

Completed
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
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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Self-reported Bodily PainThrough 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
NameTimeMethod
Bodily Pain ResponseThrough 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 ResponseThrough 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

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