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Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement

NCT07303062 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-12-24

No results posted yet for this study

Summary

The purpose of this research study is to learn if a parenting program called Adolescent Mental Health Parenting Program for Child Adult Relationship Enhancement (AMP-CARE) can help parents have more confidence in parenting their teen and improve their knowledge about normal teen development and teen mental health. The main questions it aims to answer are:

* Does the AMP-CARE parenting program improve confidence in teen parenting and positive parenting?
* Does the AMP-CARE parenting program improve parent knowledge about mental health?

Researchers will compare participants who complete the parenting program to those who do not.

Participants will:

* Complete 2 surveys, one at the start of the study and one 6 -12 weeks later
* Half of the participants will be randomly picked to attend the 6 virtual AMP-CARE sessions right away.
* The other half will have the opportunity to attend AMP-CARE after they complete the second survey.

Conditions

  • Adolescent Behavior

Interventions

BEHAVIORAL

Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE)

The goals of AMP-CARE are to teach parents how to form a positive relationship with their teen and to teach about typical adolescent development and mental health. Each AMP-CARE session will be led by 1 or 2 trainers. About 4 to 13 parents will attend each virtual session lasting approximately 1.5 hours. Sessions will be weekly for 6 weeks. Participants are encouraged to practice the skills learned at AMP-CARE between the sessions.

Sponsors & Collaborators

  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Samantha Schilling, MD MSHP · University of North Carolina, Chapel Hill

  • Yasamin Sanii, MD · University of North Carolina, Chapel Hill

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-01
Primary Completion
2027-03-01
Completion
2027-03-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07303062 on ClinicalTrials.gov