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Recruiting NCT04278690

NCT04278690 Supporting Safe Use of Medications by Parents After Infant Discharge From the Neonatal Intensive Care Unit

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Clinical Trial Summary
NCT ID NCT04278690
Status Recruiting
Phase
Sponsor NYU Langone Health
Condition Medication Administered in Error
Study Type INTERVENTIONAL
Enrollment 425 participants
Start Date 2021-03-10
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
HELPixHELPix+Tech

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 425 participants in total. It began in 2021-03-10 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a randomized controlled study of parents of children to be discharged from the neonatal intensive care unit at Bellevue and Elmhurst hospitals. A total of 425 subjects will be recruited across two sites over preparatory phases and two primary study phases.

Eligibility Criteria

Inclusion Criteria: 1. English or Spanish-speaking 2. 18 years of age and older 3. Child discharged home with a Rx for \>1 daily liquid medication (other than multivitamin) 4. Primary person who will administers child's medications. 5. Willingness and ability to participate Exclusion Criteria: 1. Does not have a working phone number 2. Does not have access to internet (via computer/smartphone) 3. Does not have a mobile phone that receives texts. 4. Not able to return to the hospital for their child's follow-up visit 5. Visual acuity worse than 20/50 according to the Rosenbaum Pocket Screener 6. Uncorrectable hearing impairment

Contact & Investigator

Central Contact

Hsiang Shonna Yin

✉ hsiang.yin@nyulangone.org

📞 646-501-4284

Principal Investigator

Hsiang Sharon Yin

PRINCIPAL INVESTIGATOR

NYU Langone

Frequently Asked Questions

Who can join the NCT04278690 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Medication Administered in Error. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04278690 currently recruiting?

Yes, NCT04278690 is actively recruiting participants. Contact the research team at hsiang.yin@nyulangone.org for enrollment information.

Where is the NCT04278690 trial being conducted?

This trial is being conducted at New York, United States.

Who is sponsoring the NCT04278690 clinical trial?

NCT04278690 is sponsored by NYU Langone Health. The principal investigator is Hsiang Sharon Yin at NYU Langone. The trial plans to enroll 425 participants.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology