Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement
AMP-CARE
Evaluating the Impact of Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE)
1 other identifier
interventional
60
1 country
2
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 11, 2025
CompletedFirst Posted
Study publicly available on registry
December 24, 2025
CompletedStudy Start
First participant enrolled
March 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2027
December 24, 2025
December 1, 2025
1 year
December 11, 2025
December 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Parent Mental Health Literacy
Parent Mental Health Literacy was assessed with 23-item self-report measure, the Parental Child Mental Health Literacy Questionnaire. Using a 5-pt scale with endpoints of "0=strongly disagree" and "4=strongly agree," parents were asked to indicate their level of agreement with statements related to 5 constructs: mental health recognition, beliefs, knowledge, help-seeking confidence, and fear of stigma. Scores ranged from 0 to 4. Higher scores indicate greater literacy.
From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.
Secondary Outcomes (2)
Parent Self Efficacy
From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.
Promotive Parenting Practices
From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.
Study Arms (2)
AMP-CARE
EXPERIMENTALParents will attend the 6 virtual sessions with a group of about 5-10 parents and 2 facilitators. The AMP-CARE group sessions are held for about 90 minutes once per week. Sessions include didactics, role playing, vignettes, and weekly home practice to build positive parenting techniques.
Waitlist Control
NO INTERVENTIONParents in the control group will be offered the intervention after completing the second study questionnaire.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Parent or guardian of teen age 11-14 years
- Receiving primary care at selected study sites
- English speaking
You may not qualify if:
- Parents of children with severe mental illness (indicated by psychiatric hospitalization in the last 12 months or previous diagnosis of psychosis)
- Parents of children with severe developmental delay (indicated by prior diagnosis of severe neurodevelopmental impairment, global developmental delay, severe expressive language delay)
- Not available at time group is scheduled
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
UNC Pediatrics at Panther Creek
Cary, North Carolina, 27519, United States
UNC Children's Primary and Specialty Care at Carolina Pointe II
Chapel Hill, North Carolina, 27517, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Samantha Schilling, MD MSHP
University of North Carolina, Chapel Hill
- PRINCIPAL INVESTIGATOR
Yasamin Sanii, MD
University of North Carolina, Chapel Hill
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 11, 2025
First Posted
December 24, 2025
Study Start
March 1, 2026
Primary Completion (Estimated)
March 1, 2027
Study Completion (Estimated)
March 1, 2027
Last Updated
December 24, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share