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NOT YET RECRUITING
NCT07823062

Specialist Review of Harm Ratings for Clinical Responses Acronym: NOHARM

Sponsor: Stanford University

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine how closely potential-harm ratings assigned using the NOHARM rubric agree with independent ratings from specialty-matched physicians. The study uses reconstructed clinical consultation cases and previously generated responses written by artificial intelligence systems or physicians. The materials contain no patient identifiers or protected health information. Board-certified attending physicians from 10 medical specialties will review assigned case-response pairs through a secure website. For each response, they will indicate whether it contains an error, describe the error when applicable, and rate the greatest potential patient harm as none, mild, moderate, or severe. Reviewers will not be shown the response source, existing rubric rating, or other reviewers' ratings. Two specialists will initially review each response; a third may review it if the first two ratings differ. The study includes a development stage, possible rubric revision, and a separate validation stage.

Official title: Specialist Physician Validation of the NOHARM Harm-Rating Rubric for Clinical Responses

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

80

Start Date

2026-09-21

Completion Date

2026-10-30

Last Updated

2026-09-16

Healthy Volunteers

Yes