Improving Neurodevelopmental ouTcomes After Prenatal Cannabinoid in uTero Exposure
Recruiting
N/A
Interventional Study
Developmental Delay
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- Up to 7 Days
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 20 (estimated)
- Sponsor
- IDeA States Pediatric Clinical Trials Network · Research network
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About This Trial
The INTACT trial is a multisite pilot feasibility study aimed at testing the effectiveness of the INTACT Intervention program in improving neurodevelopmental outcomes in infants prenatally exposed to cannabinoids. The trial will enroll 20 birthing parent/infant dyads across three sites and will evaluate feasibility endpoints rather than clinical outcomes. The study duration is 22 months, including…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Birthing Parent
* Age of majority, as defined by the state of residency
* Cannabinoid use during pregnancy confirmed with self-report
* Have the ability to speak, read, and understand English
* Birthing parent who delivered at one of the hospitals where study team members have …
Contacts