ArticleJournal of medical Internet research2026
Accountable Action End Points for Evaluating Artificial Intelligence in Digital Public Health.
Article in Journal of medical Internet research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Unlabelled: AI is increasingly embedded in digital public health systems, but model performance, system deployment, message delivery, alert volume, and user engagement do not establish whether an AI-supported workflow has changed public health practice. This viewpoint proposes a public health action end point-a prespecified, auditable, AI output-specific, actor-bound, time-bound, denominator-based way to specify and measure an existing proximal process or implementation end point. It begins with a defined AI output and records the corresponding action opportunity, accountable actor, action status, and evidence concerning the AI's role in the action. A complete specification includes rules for repeated outputs, completed action, justified nonaction, missed action, unresolved cases, denominator loss, and paired safety, workload, privacy, equity, and model drift monitoring. A public health action end point is not a new causal outcome, reporting guideline, or validated surrogate for a population health benefit. An observed action rate alone does not establish that AI initiated or caused the action; causal claims require a documented attribution strategy and an appropriate comparator or causal design. The framework applies to research and production deployments but complements rather than replaces ethics review, trial registration, and jurisdiction-specific regulatory and governance obligations. It is intended to help authors, implementers, reviewers, and editors align claims with what an evaluation has actually measured.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.