A Three-Arm Randomized Feasibility Trial of AI-Initiated Clinical Decision Support in Routine Hospitalist Practice
| Registry | NCT07889063 |
|---|---|
| Status | Not yet recruiting |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: single, health services research |
| Enrollment | 20 (Estimated) |
| Sponsor | Cedars-Sinai Medical Center (Other) |
| Conditions | Clinical Decision Support |
| Interventions | AI Clinical Decision Support: Automated EHR Data Retrieval, AI Clinical Decision Support: Admission H&P Note (Other) |
| Dates | start 2026-10-01 (estimated), primary completion 2027-10-01 (estimated), completion 2027-10-01 (estimated), first posted 2026-10-22, last updated 2026-10-22 |
| Locations | 2 sites in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Clinical Decision Support All trials of AI Clinical Decision Support: Automated EHR Data Retrieval All trials of AI Clinical Decision Support: Admission H&P Note
This study will evaluate the feasibility of using artificial intelligence (AI)-generated clinical decision support during routine inpatient hospital medicine care. Participating hospitalist physicians may receive AI-generated recommendations for eligible hospitalized patients under their care. Eligible patient cases will be randomly assigned to one of three AI prompting strategies that differ in the clinical information provided to the AI system. After reviewing each recommendation, participating physicians will complete a brief survey assessing the clinical usefulness of the recommendation, how they interpreted it, and whether it was or will be incorporated into patient management.
The study will assess whether AI-generated recommendations can be successfully generated and delivered during routine clinical care and whether physicians complete the study surveys and adopt the recommendations. It will also provide preliminary information about physicians' perceptions of AI-generated recommendations across the three prompting strategies. The findings will be used to inform the design of a future larger randomized trial of AI-initiated clinical decision support.
This is a three-arm randomized feasibility trial evaluating AI-initiated clinical decision support in routine inpatient hospital medicine practice. Eligible patient cases cared for by participating hospitalist physicians will be randomized to one of three AI prompting strategies: automated electronic health record (EHR) data retrieval, automated EHR data retrieval with explicit inclusion of the admission history and physical (H\&P) note, or the admission H\&P note alone. OpenEvidence will generate a clinical decision support recommendation for each randomized case.
The recommendation will be delivered to the attending hospitalist, who will then complete a brief electronic survey assessing the clinical utility and interpretation of the recommendation and whether it was implemented or planned for implementation. The study will assess the feasibility of generating and delivering AI-initiated recommendations during routine clinical care, physician survey completion, timely survey completion, and recommendation adoption. Findings from this feasibility trial will inform the design of a future larger randomized trial.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Arm D: Automated Electronic Health Record Data Retrieval Only | Experimental | Other: AI Clinical Decision Support: Automated EHR Data Retrieval | Arm D (Data Retrieval Only): Eligible patient cases assigned to this arm will have the OpenEvidence recommendation generated using automated electronic health record (EHR) data retrieval without explicit inclusion of the admission history and physical (H\&P) note. |
| Arm DH: Automated EHR Data Retrieval + Admission H&P Note | Experimental | Other: AI Clinical Decision Support: Automated EHR Data Retrieval; Other: AI Clinical Decision Support: Admission H&P Note | Arm DH (Data Retrieval + History and Physical): Eligible patient cases assigned to this arm will have the OpenEvidence recommendation generated using automated EHR data retrieval with explicit inclusion of the admission H\&P note. |
| Arm H: Admission H&P Note Only | Experimental | Other: AI Clinical Decision Support: Admission H&P Note | Arm H (History and Physical Only): Eligible patient cases assigned to this arm will have the OpenEvidence recommendation generated using the admission H\&P note only, without automated EHR data retrieval. |
Sex: All, ages: 18 Years to any, accepts healthy volunteers
Inclusion Criteria: * Age 18 years or older. * Attending physician providing inpatient hospital medicine care at a participating Cedars-Sinai Health System site. * Expected to provide clinical care during the study period. * Willing and able to provide informed consent. Exclusion Criteria: * Declines to provide or withdraws informed consent. * Not actively providing attending-level inpatient care on a participating hospitalist service during the study period. * Unable to complete study procedures.
| Facility | City | Country | Status |
|---|---|---|---|
| Cedars-Sinai Medical Center | Los Angeles, California | United States | |
| Huntington Hospital | Pasadena, California | United States |