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Clinical Trials/NCT03798756
NCT03798756
Completed
N/A

Automated Check-in Data Collection Study

Keele University1 site in 1 country9,274 target enrollmentJanuary 14, 2019
ConditionsPrimary Care

Overview

Phase
N/A
Intervention
Not specified
Conditions
Primary Care
Sponsor
Keele University
Enrollment
9274
Locations
1
Primary Endpoint
Self-reported Bodily Pain
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 14, 2019
End Date
April 14, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Self-reported Bodily Pain

Time Frame: 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 Outcomes

  • Bodily Pain Response(Through study completion at 1st visit (Day 1))
  • Consent to Contact Response(Through study completion at 1st visit (Day 1))

Study Sites (1)

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