Viewing Study NCT07402668


Ignite Creation Date: 2026-03-26 @ 3:15 PM
Ignite Modification Date: 2026-03-31 @ 12:25 AM
Study NCT ID: NCT07402668
Status: RECRUITING
Last Update Posted: 2026-02-17
First Post: 2026-01-27
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Does AI Make Clinicians More Appropriately Confident? A Randomized Study in Preterm Birth Prediction
Sponsor: Rigshospitalet, Denmark
Organization:

Study Overview

Official Title: Does AI Make Clinicians More Appropriately Confident? A Randomized Study in Preterm Birth Prediction
Status: RECRUITING
Status Verified Date: 2026-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this randomized questionnaire-based study is to evaluate how different presentations of artificial intelligence (AI) decision support influence clinical judgment among medical doctors working in obstetrics and gynecology when assessing the risk of spontaneous preterm birth using clinical case vignettes with cervical ultrasound images. The study specifically compares two AI presentation formats: a binary classification (preterm vs term birth) and an individualized risk estimate of preterm birth.

The main questions it aims to answer are:

* Which AI presentation format leads to better alignment between clinicians' confidence and decision accuracy (diagnostic calibration)?
* Do different AI presentation formats lead to helpful or harmful changes in clinical decisions?

Participants will complete an online questionnaire in which they review clinical cases, make diagnostic and management decisions, rate their diagnostic confidence before and after seeing the AI output, and report their trust in the AI.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: