AI and home videos could spot cerebral palsy months earlier
NCT ID NCT04287166
First seen Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time
Summary
This study explores whether a new screening procedure can detect cerebral palsy (CP) earlier in high-risk infants using video recordings and artificial intelligence. Traditionally, CP is diagnosed between 12 and 24 months of age, but earlier detection could lead to better outcomes. Researchers will have parents and healthcare workers record infant movements on video, which will be analyzed remotely by experts and by machine learning models. The goal is to see if this remote approach is feasible and accurate enough to be used across a wide region.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this approach could enable earlier diagnosis and intervention for cerebral palsy, improving motor function and quality of life for affected children.
- What could go wrong
- This is a feasibility study with a small sample size, so results may not be generalizable. The AI and remote video methods may not match the accuracy of in-person expert assessments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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100 people
The number who actually took part.
- Started
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Aug 2020
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
High-risk infants referred to high-risk follow-up at discharge from one of the participating Neonatal Intensive Care Units, are candidates for enrollment. Following review of the inclusion and exclusion criteria, eligible subjects will be invited to participate. All subjects (parents) must give written informed consent prior to any study procedures being carried out.
- Ages
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0 to 2 months
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * hospitalized at a Neonatal Intensive Care Unit (NICU) within the Central Norway Regional Health Authority that is referred to follow-up in the Specialist Health Services containing a team of minimum a pediatrician and a physiotherapist. * at high-risk for adverse neurological outcomes as considered by the pediatrician on the basis of clinical judgement (example: serious asphyxia, prematurity, stroke, brain hemorrhage) Exclusion Criteria: * Peripheral neuromotor disease e.g. brachial plexus injury * iatrogenic restricted movements (e.g. cast for clubfoot)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of Pediatrics, Møre and Romsdal Hospital Trust
Ålesund, Norway
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Department of Pediatrics, Nord-Trøndelag Hospital Trust
Levanger, Norway
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Department of Pediatrics, St. Olav's Hospital Trust
Trondheim, Norway
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Other studies related to the condition(s) this trial covers.
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