FideAI

FID-083 · Open question

Healthcare Evidence, Escalation, and Human Control

When should a healthcare-adjacent AI system surface uncertainty, seek qualified review, or stop an action, and can the receiving human meaningfully retain control?

Why the question remains open

A technically correct response can still omit context or fail to reach the right person. Trustworthy assistance requires evidence fidelity and workable escalation, including whether a human can understand and correct the system's contribution.

Working hypothesis

A proposition to test, not a finding.

Evidence-linked uncertainty and role-specific handoffs will improve detection and correction of consequential errors over generic disclaimers. Excessive escalation may instead cause overload and missed signals.

Proposed method

How the question could be tested

  • 01Co-design synthetic care-navigation and clinical-evidence-summary scenarios with qualified clinicians and care practitioners; define intended use and excluded uses.
  • 02Compare generic warnings, structured uncertainty, and evidence-linked handoffs under missing context, conflicting sources, and time pressure.
  • 03Measure source fidelity, recognition of out-of-scope cases, escalation appropriateness, receiving-reviewer comprehension, correction rates, and workload.

Needed controls

What must constrain the study

  • 01Begin with simulation only: no real patient records, diagnosis, treatment, or live care decisions. Any later human study requires appropriate ethics review and consent.
  • 02Use independent clinical adjudication and report disagreement. Separate technical accuracy, workflow usability, and patient outcomes.
  • 03Disclose assumptions about who can decide, what risks warrant escalation, and whose perspective informs the task set.

Relationship to existing work

Complements FID-010 and FID-018 while retaining their faith and pastoral contexts. Uses the general evidence and authority questions in FID-078.

Expected outputs

Artifacts the work should produce

  • 01A reviewed simulation protocol and safe exemplar cases.
  • 02An evidence and handoff assessment framework with explicit clinical limits.

Open questions

Uncertainties the protocol must resolve

  • 01When does escalation preserve control rather than shift an unmanageable burden?
  • 02Which populations and care settings are not represented by initial scenarios?

Open question

Open work

Primary need: clinical review, care workflow expertise, human factors, evaluation design

  • Clinicians, care practitioners, and patient advocates to shape requirements.
  • Human-factors and evaluation researchers to test receiving-human control.