Automated Check-in Data Collection Study

Primary Care Clinical Trial

— ACDC  

Official title:

Automated Check-in Data Collection Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03798756
• Other study ID #: RG-0275-18 V1.0
• Status: Completed
• Start date: January 14, 2019
• Est. completion date: April 14, 2019

Study information

• Verified date: March 2021
• Source: Keele University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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 information / eligibility

• Status: Completed
• Enrollment: 9274
• Est. completion date: April 14, 2019
• Est. primary completion date: April 14, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Primary Care

Locations

Country	Name	City	State
United Kingdom	New Cross Hospital	Wolverhampton

Sponsors (1)

Lead Sponsor	Collaborator
Keele University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Self-reported Bodily Pain	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.	Through study completion at 1st visit (Day 1)
Secondary	Bodily Pain Response	Proportion of participants answering the bodily pain research question using an automated check-in screen.	Through study completion at 1st visit (Day 1)
Secondary	Consent to Contact Response	Proportion of participants answering the consent to contact research question using an automated check-in screen.	Through study completion at 1st visit (Day 1)