Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Pilot Study of a Remote ADHD Monitoring Program

RAMP is a pilot study examining the use of an Attention-Deficit/Hyperactivity Disorder (ADHD) Monitoring Program during the early stages of treating ADHD in children living in rural settings. This trial will enroll 36 caregiver/infant dyads across 2 sites and will evaluate feasibility endpoints rather than clinical outcomes. Enrolled participants will be randomized 1:1 to the intervention group (RAMP reports) or control group (digital education handouts). The study duration is 10 months, including start-up, enrollment and intervention, and data analysis and manuscript submission.

Participants needed: 36
Trial details
Age: 5-11Biological sex: AllType: InterventionalSponsor: IDeA States Pediatric Clinical Trials NetworkUpdated: Apr 28, 2026Locations: 2
Eligibility criteria

be under the care of a participating provider [+13]

has serious mental health comorbidities (Children with depression, anxiety, oppo... [+3]

Status: Recruiting

Talk With Me Baby to Enhance the Early Home Language Environment

The goal of this clinical trial is to learn if the Talk With Me Baby (TWMB) program improves the home-language environment for at-risk families with children ages two to six months when primary care providers deliver the program during well-child checkups. The main question it aims to answer is: Will the TWMB program increase the time a caregiver talks to their infant? Participants will: 1. Come to at least four well-child checkups 2. Receive the TWMB program from the provider during the checkups 3. Record their conversations with their infant before they receive the program and after they receive the program four times.

Participants needed: 66
Trial details
Age: 0-9Biological sex: AllType: InterventionalSponsor: IDeA States Pediatric Clinical Trials NetworkUpdated: Aug 29, 2025Locations: 2
Eligibility criteria

A caregiver who will receive TWMB during routine WCC visits for their child at p... [+8]

Status: Recruiting

Improving Neurodevelopmental ouTcomes After Prenatal Cannabinoid in uTero Exposure

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 study start-up, enrollment and intervention, and data analysis and manuscript preparation.

Participants needed: 20
Trial details
Age: Up to 7Biological sex: AllType: InterventionalSponsor: IDeA States Pediatric Clinical Trials NetworkUpdated: Jun 24, 2025Locations: 3
Eligibility criteria

Age of majority, as defined by the state of residency [+9]

Other illicit drug use, excluding cannabinoids, during pregnancy (such as heroin... [+5]