Trial · NCT07883304
AI-CLINIC: A Prospective Multisite Feasibility and Safety Study of AI-Assisted Pre-Consultation History-Taking in Outpatient Cardiology
NCT07883304, Not yet recruiting, London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. AI-CLINIC: A Prospective Multisite Feasibility and Safety Study of AI-Assisted Pre-Consultation History-Taking in Outpatient Cardiology. Trials, record NCT07883304. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07883304
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- AI-CLINIC: A Prospective Multisite Feasibility and Safety Study of AI-Assisted Pre-Consultation History-Taking in Outpatient Cardiology
- NCT number
- NCT07883304
- Status
- Not yet recruiting
- Enrollment
- 60 participants, estimated
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Conditions
- Symptom Tracking, Cardiology, Medical History Taking
- Interventions
- AI Interview
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Usability | Baseline | Successful completion is defined as completion of the AI interview with a readable, clinically reviewable summary generated and accessible to the treating clinician before the clinician begins the consultation. A summary is usable if not blank, corrupted, or rendered unusable by technical failure; it need not be clinically perfect. Completion may occur at home or through rescue; availability is defined independently of whether the clinician opened the summary (the attestation captures actual use). The primary analysis includes all consented participants whose eligible in-person appointment proceeds and who have an opportunity to receive the study intervention. Failure to receive, initiate, or complete the interview - including technical failure or participant refusal after consent - is counted as unsuccessful completion. |
| Secondary | 1) Patient engagement with the chatbot | Baseline | Measured by the Conversation-Turns Per Session, a validated metric defined as the total number of alternating input-output pairs during the interaction and used as a proxy for depth and fluidity of patient-chatbot interaction \[11\]. For context, CPS values typically range from 1-3 in digital assistants (such as Siri), around 9 in human dialogue, and ≥23 in advanced social chatbots such as Microsoft's Xiaolce \[25\]. |
| Secondary | Objective durations | Baseline | Interview duration (platform); physician-encounter duration (room-entry to room-exit, where recorded); scheduled slot length as context; summarized overall and by setting. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07883304
GET https://conductscience.org/api/trials/v1/NCT07883304/registered