Trial Outcomes & Findings for Automated Check-in Data Collection Study (NCT NCT03798756)

Results Overview

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.

Recruitment status

COMPLETED

Target enrollment

9274 participants

Primary outcome timeframe

Through study completion at 1st visit (Day 1)

Results posted on

2021-04-19

Participant Flow

Participant milestones

Participant milestones
Measure	Cohort Automated check-in
Overall Study STARTED	9274
Overall Study COMPLETED	9274
Overall Study NOT COMPLETED	0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure	Cohort n=9274 Participants This was a Cohort, there were no arms. It was an entire group.
Age, Categorical <=18 years	0 Participants n=9274 Participants
Age, Categorical Between 18 and 65 years	5982 Participants n=9274 Participants
Age, Categorical >=65 years	3292 Participants n=9274 Participants
Sex: Female, Male Female	5653 Participants n=9274 Participants
Sex: Female, Male Male	3621 Participants n=9274 Participants
Region of Enrollment United Kingdom	9274 participants n=9274 Participants
Patients checking in for a consultation, answering a research question, using check-in sceen	9274 Participants n=9274 Participants

PRIMARY outcome

Timeframe: 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.

Outcome measures

Outcome measures
Measure	Bodily Pain n=9274 Participants To assess patient acceptability of answering a research question on bodily pain, in the general practice waiting room using an automated check-in screen.
Self-reported Bodily Pain None	2937 Participants
Self-reported Bodily Pain Very mild	1061 Participants
Self-reported Bodily Pain Mild	1446 Participants
Self-reported Bodily Pain Moderate	2344 Participants
Self-reported Bodily Pain Severe	1125 Participants
Self-reported Bodily Pain Very Severe	9 Participants
Self-reported Bodily Pain Not documented	352 Participants

SECONDARY outcome

Timeframe: Through study completion at 1st visit (Day 1)

Proportion of participants answering the bodily pain research question using an automated check-in screen.

Outcome measures

Outcome measures
Measure	Bodily Pain n=9274 Participants To assess patient acceptability of answering a research question on bodily pain, in the general practice waiting room using an automated check-in screen.
Bodily Pain Response	8922 Participants

SECONDARY outcome

Timeframe: Through study completion at 1st visit (Day 1)

Proportion of participants answering the consent to contact research question using an automated check-in screen.

Outcome measures

Outcome measures
Measure	Bodily Pain n=9274 Participants To assess patient acceptability of answering a research question on bodily pain, in the general practice waiting room using an automated check-in screen.
Consent to Contact Response	8285 Participants

Adverse Events

Cohort

Serious events: 0 serious events

Other events: 0 other events

Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Mrs Sarah Lawton

Keele University

Phone: 01782 734887

Email: [email protected]

Results disclosure agreements

Principal investigator is a sponsor employee
Publication restrictions are in place