← Eichor
Study identifier: NCT06521918 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Combined Artificial Intelligence and Mobile Application for Remote Infant Motor Screening: Development and Validation

Condition: Motor Disorders  ·  Sponsor: National Taiwan University Hospital

PhaseN/A
Planned participants242
Who can joinAll sexes, 2 Months to 18 Months
Healthy volunteersYes

About this study

The purpose of this study is therefore five-fold: (1) designation of an APP "Baby Go" version 3.0 to include the assessment, follow-up, and education functions for parental use at home, (2) development and validation of the AI algorithm for infant motor assessment based on home videos obtained from term and preterm infants, (3) comparison of parental perception and report with AI-driven assessment results, (4) examination of the predictive validity of the AI algorithm for infant motor assessment on subsequent outcome, and (5) investigation of the usability of the APP "Baby Go" version 3.0 in parents and clinicians.

This description comes directly from the study's public registry record.

Talk to the study team

Suh-Fang Jeng, Professor  ·  886-2-33668132  ·  jeng@ntu.edu.tw

Always discuss trial participation with your own doctor first.

Locations (1)

National Taiwan UniversityTaipei, Taiwan, 100, TaiwanRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06521918