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Measuring AI Reliance Among Intern Doctors in Palestine (AI-RP)

23. april 2026 opdateret af: Al-Quds University

AI Reliance in Diagnostic Radiology Among Intern Doctors in Palestine: A Triple-Arm, Triple-Blind, Parallel-Design Randomized Controlled Trial

This study aims to enroll intern doctors and have them sit one of three identical radiology exams. The only difference between them is an AI-assistant. The differences between these groups will be used to measure the extent of AI reliance among intern doctors in Palestine.

Studieoversigt

Detaljeret beskrivelse

This is a triple-arm trial investigating AI reliance in radiology among intern doctors in Palestine. The study will involve a radiology exam with three versions, a control, a sham AI (Correct answer) version, and a sham AI (incorrect answer) version. By comparing differences between the three groups, we aim to quantify AI reliance among this patient population.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

159

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

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

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Intern doctor in Palestine
  • Completion of at least 3 months from their 1 year internship
  • Confirmed prior training in radiologic interpretation

Exclusion Criteria:

  • Does not consent to the study
  • Completion of the internship
  • Non-completion of at least 3 months of their 1 year internship

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: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Control-No AI
Subjects in this arm will undergo the base exam, without an AI assistant, and without the knowledge that an AI assistant is used among other groups.
Eksperimentel: Experimental-Correct AI
Subjects in this arm will undergo the base exam, with an AI assistant, that provides the correct answer.
This is a suggested answer in the guise of an AI assistant. The prompt was written by the authors and not an actual AI chat model. The suggested answer is correct.
Sham-komparator: Sham Comparator-Incorrect AI
Subjects in this arm will undergo the base exam, with an AI assistant, that provides an incorrect answer.
This is a suggested answer in the guise of an AI assistant. The prompt was written by the authors and not an actual AI chat model. The suggested answer is incorrect.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
AI Reliance
Tidsramme: Periprocedural

The extent of dependance of subjects on AI. It will be estimated based on a difference in mean score between the groups. We will also assess this outcome by creating an (AI-concordance field: for the intervention groups it will be how many times the subjects answered identically to the AI prompt, while for the control group it will be 0).

AI reliance will be operationalized as:

AI Reliance = Mean score improvement in the correct-AI group vs control Mean score decrement in the incorrect-AI group vs control

We will compare the two different outcome measures to determine which better represents our outcome.

Periprocedural
Exam time
Tidsramme: Periprocedural
This will be defined as the length of time subjects spend completing the exam.
Periprocedural

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Correlation of baseline characteristics with AI reliance
Tidsramme: Baseline

We will measure specific variables and their correlation with increased AI reliance.

For this measure, we will depend on self-reported via a post-exam survey and include: gender, region, current clinical exposure, and current radiological exposure.

We will then demonstrate the % of patients with the aforementioned characteristics and the differences in AI reliance in those aspects.

Baseline
% of Subjects with a positive Perception of AI use in Radiology, and its correlation with AI reliance
Tidsramme: Baseline

We will measure AI perception in radiology among subjects and its effect on their AI reliance. This will be done via a scale described in the literature, and by assessment of the % of subjects who have a positive, or negative outlook or perception on AI use in radiology. We will further test the relationship between AI reliance and AI perception.

This will be done through the use of the scale described (Radiology Residents' Perceptions of Artificial Intelligence: Nationwide Cross-Sectional Survey Study) by Chen et al.

Baseline
% of radiology interest as a specialty and its correlation with AI reliance
Tidsramme: Baseline

We will measure radiology interest and its association with AI reliance.

For this measure, we will use a validated tool for the measurement of radiology interest, described in the following study: "Assessing diagnostic radiology knowledge among Syrian medical undergraduates"

We will then demonstrate the % of patients interested in specializing in radiology and the differences in AI reliance in those aspects.

Baseline

Samarbejdspartnere og efterforskere

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

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

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 (Anslået)

10. april 2026

Primær færdiggørelse (Anslået)

1. maj 2026

Studieafslutning (Anslået)

1. maj 2026

Datoer for studieregistrering

Først indsendt

1. april 2026

Først indsendt, der opfyldte QC-kriterier

23. april 2026

Først opslået (Faktiske)

30. april 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

30. april 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. april 2026

Sidst verificeret

1. marts 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 697/REC/2026

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

IPD-planbeskrivelse

As the data includes private information, particularly in the form of exam scores, we will opt out of sharing the study data.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

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 .

Kliniske forsøg med Praktik og ophold

Kliniske forsøg med AI prompt (Correct)

Abonner