Clinical trial Recruiting at 1 site Interventional

AI feedback on fetal weight estimates across clinician experience levels

Official title: Evaluating the Sensitivity to Change of AI-Feedback in Ultrasound Biometry: A Stratified Randomized Controlled Trial Across the Expertise Gradient

Run by Copenhagen Academy for Medical Education and Simulation · NCT07476638 · Data updated 2026-11-12

A real-time AI help is tested to see if it makes fetal weight estimates from ultrasound more accurate, especially for novices and intermediates, compared with doing it manually.

More Fetal Weight trials

Quick facts

Study typeInterventional
SexAll
Enrollment75 (estimated)
SponsorCopenhagen Academy for Medical Education and Simulation
Academic / other
Locations3 sites (Hillerød, Capital Region and 2 other locations)
StatusRecruiting
StartedMarch 1, 2026
Main results expectedMarch 1, 2027
Study endsMarch 1, 2027
Registry record updatedAugust 6, 2026
Trial IDNCT07476638 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthcare professionals and students in obstetrics, including medical students, residents, and senior consultants, who can communicate in Danish or English.

Probably not a fit

Participants with barriers to AI use or non-communicable limitations may not experience improved accuracy.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized trial assigns 75 participants across three expertise levels (novice, intermediate, expert) to AI-assisted or manual ultrasound biometry. The primary outcome is the accuracy of estimated fetal weight (MAPE) compared to birthweight. Secondary outcomes include procedure time, image quality, error from baseline scans, and cognitive workload measured by NASA-TLX. The study probes the Expertise Reversal Effect to see if AI benefits diminish with higher user experience. Real-time AI provides automated plane validation and calipers to the ultrasound workflow.

Why it matters

Potential benefit: If successful, AI feedback could improve fetal weight estimation accuracy and efficiency, potentially guiding better clinical decisions.

How similar studies have gone: Prior work suggests AI-assisted imaging can improve measurements, but the reversal of benefit by experience level is a novel aspect in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Clinical Target Population: Healthcare professionals and students, including but not limited to:

* Medical students (doing their masters.
* Resident physicians and Senior Consultants in Obstetrics and Gynecology.

Exclusion:

\- If the participants do not understand and speak either Danish or English

Pregnant women:

Inclusion Criteria:

* Pre pregnancy BMI \< 40
* Singelton pregnancy
* GA ≥ 37+0 at time of induction
* Intact membranes (to ensure consistent amniotic fluid index)

Exclusion Criteria:

* Major fetal anatomical anomaly
* Anhydramnios (DVP \< 2 cm)
* CPR ratio \< 2.5th percentile

Where it's running

  • Rigshospitalet
    Copenhagen, København Ø, Denmark
    Recruiting
  • Nordsjællands Hospital
    Hillerød, Capital Region, Denmark
    Not yet recruiting
  • Rigshospitalet
    Copenhagen, København Ø, Denmark
    Enrolling by invitation

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • AI ultrasound tool to estimate fetal weight before delivery

    A AI-enabled ultrasound test is being tried in 1,000 pregnant people to see how accurately it can predict fetal weight compared with standard specialist measurements.

    Recruiting at 2 sites University of North Carolina, Chapel Hill · New Orleans, Louisiana and 5 other locations · NCT07661433

  • Ultrasound try to predict macrosomia at term

    This study tests how well ultrasound weight estimates predict a baby’s birth weight in pregnancies with suspected macrosomia.

    Recruiting Centre Hospitalier Henri Duffaut - Avignon · Avignon · NCT07433751

  • Heart risk check for young women 3–6 years after pregnancy with or without placental complications.

    This project will test an app-based algorithm to see if it can identify cardiovascular risk in women 3–6 years after giving birth, including those who had preeclampsia or low-birth-weight infants.

    Recruiting Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · Barcelona · NCT07356817

  • Comparing ultrasound and MRI for estimating fetal weight in large babies

    This study is testing whether ultrasound or MRI is better at estimating the weight of large babies before birth for pregnant women who might have macrosomia.

    Recruiting Western Galilee Hospital-Nahariya · Nahariya · NCT06898892

  • Fetal Heart Function in Growth-Restricted Pregnancies

    This study tests whether fetal echocardiography using a modified Tei index (Mod-MPI) can reveal early heart changes in pregnancies affected by fetal growth restriction (IUGR).

    Recruiting Assiut University · Asyut · NCT07760194

  • Combined first-trimester screening for pregnancy complications

    This project tests a standardized first-trimester screening to see if it can identify pregnant women at 11–13 weeks who are at higher risk for preeclampsia, fetal growth restriction, chromosomal problems, and other serious complications.

    Recruiting at 3 sites Institute of Health Information and Statistics of the Czech Republic · Most, Czechia and 2 other locations · NCT07015203

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.