Trial · NCT07889063
Artificial Intelligence (AI)-Initiated Clinical Decision Support in Hospitalist Practice
NCT07889063, Not applicable, Not yet recruiting, Cedars-Sinai Medical Center
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Artificial Intelligence (AI)-Initiated Clinical Decision Support in Hospitalist Practice. Trials, record NCT07889063. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889063
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Artificial Intelligence (AI)-Initiated Clinical Decision Support in Hospitalist Practice
- NCT number
- NCT07889063
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 20 participants, estimated
- Lead sponsor
- Cedars-Sinai Medical Center
- Conditions
- Clinical Decision Support
- Interventions
- AI Clinical Decision Support: Automated EHR Data Retrieval, AI Clinical Decision Support: Admission H&P Note
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Successful AI Recommendation Delivery Rate | Within 24 hours of hospital admission | Proportion of randomized patient cases in which an AI-generated recommendation is successfully delivered to the attending hospitalist. |
| Primary | Physician Survey Completion Rate | Within 48 hours after AI recommendation delivery | Proportion of successfully delivered AI-generated recommendations for which the attending hospitalist completes the electronic physician survey. |
| Primary | Timely Physician Survey Completion Rate | Within 12 hours of AI recommendation delivery | Proportion of successfully delivered AI-generated recommendations for which the attending hospitalist completes the electronic physician research survey within 12 hours of recommendation delivery. |
| Primary | Recommendation Adoption Rate | Within 48 hours after AI recommendation delivery | Proportion of AI-generated recommendations that the attending hospitalist reports as implemented or planned for implementation. Responses will be recorded separately as implemented, planned but not yet implemented, or not adopted. |
| Secondary | Physician-Perceived Clinical Utility | Within 48 hours after AI recommendation delivery | Physician-perceived clinical utility of the AI-generated recommendation, assessed at the patient-case level using a single-item 0-10 numeric rating scale, with anchors at 0 ("Not at all useful"), 5 ("Moderately useful"), and 10 ("Extremely useful"). |
| Secondary | Interpretation of AI-Generated Recommendations | Within 48 hours after AI recommendation delivery | Physician interpretation of the AI-generated recommendation, assessed using six predefined response categories in the physician research survey. |
| Secondary | Physician-Reported Recommendation Adoption Status | Within 48 hours after AI recommendation delivery | Physician-reported adoption of the AI-generated recommendation, categorized as implemented, planned but not yet implemented, or not adopted. |
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/NCT07889063
GET https://conductscience.org/api/trials/v1/NCT07889063/registered