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Recruiting NCT06197997

NCT06197997 Resilient, Engaged, and Connected Study

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Clinical Trial Summary
NCT ID NCT06197997
Status Recruiting
Phase
Sponsor Johns Hopkins University
Condition Parenting
Study Type INTERVENTIONAL
Enrollment 840 participants
Start Date 2024-09-01
Primary Completion 2028-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Chicago Parent Program (CPP)

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 840 participants in total. It began in 2024-09-01 with a primary completion date of 2028-06-30.

⚠ 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

Purpose of this study is to test the effectiveness and implementation of an evidence-based parenting intervention for improving parenting and school outcomes in a sample of 4-5-year-old children enrolled in public prekindergarten (PreK) programs in Maryland.

Eligibility Criteria

Inclusion Criteria: Public school or Community School in Baltimore City, Cecil County, or Harford County serving at least 40% of students meeting eligibility for low-income or located in a community designated as high need by the Maryland State Department of Education based on a score of 0.6 on the Center for Disease Control Social Vulnerability Index: * has at least 1 full-day public PreK classroom with 20+ students; * school has not offered CPP in the prior 3 years; * principal consents to being randomized and participate for 2 years; * principal consents to study team recruiting parents, teachers, and staff to participate in the study. PreK Parents: * Parent (biological, step, adoptive, foster), grandparent, or legal guardian of 4-5 year old student enrolled in participating PreK program; * 18+ yrs; * speaks English or Spanish; * consents to allowing access child's school identification. Teachers: * PreK or K teacher in classroom of student of participating parent; * consents to completing study surveys. CPP Group Leaders: * completes CPP group leader training * agrees to lead CPP groups * speaks English or Spanish * at least a High School diploma/General Equivalency Diploma (GED) * consents to completing surveys and submitting audio recorded CPP sessions for fidelity assessment School-based personnel inclusion criteria: * Principal, teacher, or other school-based staff involved in CPP implementation * consents to interview on perspectives about CPP in the school Exclusion Criteria: * Principal cannot commit staff to offering CPP groups * school previously offered CPP in prior 3 years * school located in a geographic area with less than 80% connectivity * PreK Parents previously participated in CPP * Teachers: teacher also a participating parent or CPP group leader * School-based personnel: Principal, teacher, or other school-based staff is a study parent

Contact & Investigator

Central Contact

Deborah Gross, DNSc

✉ debgross@jhu.edu

📞 410-614-5311

Principal Investigator

Deborah Gross, DNSc

PRINCIPAL INVESTIGATOR

JHU School Of Nursing

Frequently Asked Questions

Who can join the NCT06197997 clinical trial?

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

Is NCT06197997 currently recruiting?

Yes, NCT06197997 is actively recruiting participants. Contact the research team at debgross@jhu.edu for enrollment information.

Where is the NCT06197997 trial being conducted?

This trial is being conducted at Baltimore, United States, Baltimore, United States.

Who is sponsoring the NCT06197997 clinical trial?

NCT06197997 is sponsored by Johns Hopkins University. The principal investigator is Deborah Gross, DNSc at JHU School Of Nursing. The trial plans to enroll 840 participants.

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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