Automated Check-in Data Collection Study

NCT03798756 | Completed Results

• 1 other identifier: RG-0275-18 V1.0
• Study Type: observational
• Target: 9,274
• Locations: 1 country
• Sites: 1

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.

Conditions

Primary Care

Outcome Measures

Primary Outcomes (1)

• 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 Outcomes (2)

• Bodily Pain Response

  Through study completion at 1st visit (Day 1)

• Consent to Contact Response

  Through study completion at 1st visit (Day 1)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

All patients of age 18 and over, who can read and respond in English and with a booked appointment, consulting with any Health Care Professional (HCP) at their general practice, during the recruitment period will be eligible to participate. All patients are required to confirm their attendance at the general practice by using the automated check-in screen. If the patient completing the automated check-in screen is 18 years of age or over, the additional two research questions will appear for completion.

You may qualify if:

• 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.

You may not qualify if:

• Patients under the age of 18 attending the general practice for a consultation with a healthcare professional.

Sponsors & Collaborators

• Keele University: lead

Study Sites (1)

New Cross Hospital

Wolverhampton, WV10 0QP, United Kingdom

Location

Results Point of Contact

• Title: Mrs Sarah Lawton
• Organization: Keele University

s.a.lawton@keele.ac.uk

01782 734887

Study Officials

• Christian D Mallen

  University of Keele

  STUDY DIRECTOR

Publication Agreements

• PI is Sponsor Employee: Yes

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 14, 2018
• First Posted: January 10, 2019
• Study Start: January 14, 2019
• Primary Completion: April 14, 2019
• Study Completion: April 14, 2019
• Last Updated: April 19, 2021
• Results First Posted: April 19, 2021

Record last verified: 2021-03

Locations

GB (1)