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Evaluating the Preferences and Tradeoffs of AI-based Electronic Consultations for Older Adults in Primary Care

8. september 2026 opdateret af: Gary Weissman, University of Pennsylvania

Evaluating the Safety and Appropriateness of AI-based E-Consults for Older Adults in Primary Care

Electronic consultations, or e-consults, let a primary care doctor request medical advice from a specialist without requiring the patient to attend a separate visit. Artificial intelligence (AI) systems may be able to provide this type of advice, potentially making e-consults faster and less costly. However, whether AI-based e-consults are acceptable may depend on how patients and clinicians weigh factors such as who provides the advice, how quickly it is received, its cost, and its quality.

The purpose of this study is to examine how older adult patients and primary care clinicians weigh these factors when comparing e-consults produced by a human specialist with those produced by an AI system. In the study, participants will complete a one-time survey in which they compare sets of two hypothetical e-consults. Each e-consult will include a different combination of features, such as whether the advice comes from a human or AI, the expected wait time, the cost, and the quality of the advice. This study will estimate how much patients and clinicians value each feature in an e-consult. The findings will inform the potential future AI e-consults, so they better reflect patient and clinician preferences.

Studieoversigt

Status

Rekruttering

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

220

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

PATIENTS:

Inclusion Criteria:

  • Adult, 65 years of age or older
  • Had at least two office visits at Penn Medicine in the past 12 months
  • Has an upcoming appointment in a Penn Medicine primary care setting, including family medicine, internal medicine, and geriatric medicine

Exclusion Criteria:

  • Documented Alzheimer's, dementia, or related condition

CLINICIANS:

Inclusion Criteria:

  • Adult, 18 years of age or older
  • Works at Penn Medicine as one of the following: physician, nurse practitioner, or physician's assistant
  • Works in a primary care Penn Medicine setting including: family medicine, internal medicine, geriatrics medicine

Exclusion Criteria:

  • Actively in medical school, internship, or residency

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Electronic Consultation Systems
Participants will review 2 different e-consult systems, which will differ in terms of quality, cost, wait time, and source of the e-consult. Participants will then indicate a preference for 1 e-consult system in each set.
Participants will review these e-consults systems via a one-time survey lasting about 15 minutes.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Preferences and Tradeoffs of Attributes of Electronic Consults
Tidsramme: From enrollment to the end of the survey, approximately 15 minutes
Participants will review 12 sets comparing 2 hypothetical e-consults. Each e-consult is defined by five attributes: the source (i.e., AI vs. human), wait time, cost, and quality of the e-consult, as well as, whether follow-up questions can be asked. For each set, the outcome is the participant's selection of one e-consult over the other. We will analyze the results of the discrete choice experiment using mixed-effects logistic regression adjusted for each attribute value with crossed random effects (intercepts) for participant and task.
From enrollment to the end of the survey, approximately 15 minutes

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Health Numeracy Measured by the Short Numeracy Understanding in Medicine Instrument
Tidsramme: From enrollment to the end of the survey, approximately 15 minutes
Health numeracy will be measured using the 8-item Short Numeracy Understanding in Medicine instrument (S-NUMi). Each correct response contributes one point to the total score. Total scores range from 0 to 8, with higher scores indicating greater health numeracy.
From enrollment to the end of the survey, approximately 15 minutes

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

3. september 2026

Primær færdiggørelse (Anslået)

1. december 2026

Studieafslutning (Anslået)

1. december 2026

Datoer for studieregistrering

Først indsendt

9. august 2026

Først indsendt, der opfyldte QC-kriterier

9. august 2026

Først opslået (Faktiske)

14. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. september 2026

Sidst verificeret

1. august 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 26-5862

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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