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RecruitingNCT07303062AMP-CAREUpdated Sep 18, 2026

Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement

An interventional study of Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE) in Adolescent Behavior, sponsored by University of North Carolina, Chapel Hill. Recruiting at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by University of North Carolina, Chapel Hill · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

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.
Read the detailed description

In this randomized controlled trial, 60 parents of teens, ages 11-14 years, will be randomized to either AMP-CARE or wait-list control to achieve the following aims:

AIM 1. To measure the impact of AMP-CARE on parent mental health literacy as measured by the Parental Child Mental Health Literacy Questionnaire (PCMHLQ).

AIM 2: To measure the impact of AMP-CARE on parenting self-efficacy as measured by the Parenting Self Efficacy Scale.

AIM 3: To measure the impact of AMP-CARE on promotive parenting practices assessed by the Positive Parenting and Parental Involvement subscales of the Alabama Parenting Questionnaire.

02

Conditions studied

  • Adolescent Behavior

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Keywords

  • teen parenting program
  • teen mental health
  • mental health stigma
  • positive parenting
  • parenting self-efficacy
03

In context

Adolescent Behavior

305 studies on the registry are indexed under Adolescent Behavior; 47 are open to participants now.

This study's planned enrollment of 60 is below the median of 172 across 256 interventional studies indexed under Adolescent Behavior.

Browse Adolescent Behavior studies →

Lead sponsor

University of North Carolina, Chapel Hill is the lead sponsor of 1,372 studies on the registry; 133 are open to participants now.

Of its 161 completed or terminated interventional studies of FDA-regulated products, 139 (86%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Parent or guardian of teen age 11-14 years
  • Receiving primary care at selected study sites
  • English speaking

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    AMP-CARE

    Parents 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.

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

  • No intervention
    Waitlist Control

    Parents in the control group will be offered the intervention after completing the second study questionnaire.

Interventions

  • BehavioralAdolescent 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.

06

What researchers measure

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.

    Time frame: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.

Secondary outcomes

  1. Parent Self Efficacy

    Parenting self-efficacy was assessed with the 19-item self-report measure Parenting Self Efficacy Scale. Using a 5-point scale, parents indicated how frequently states related to their efficacy to develop positive teenager behavior, their efficacy to respond competently to negative teenager behavior, and their monitoring efficacy were true from "1=never" to 5 "always." Total scores ranged from 1 to 5 with higher scores indicating greater self-efficacy.

    Time frame: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.

  2. Promotive Parenting Practices

    Promotive parenting practices were assessed with 16 self-report items from two subscales of Alabama Parenting Questionnaire. The positive involvement subscale includes 10 items, with a range of possible scores from 10 to 50. The positive parenting subscale includes 6 items, with a range of possible scores from 6 to 30. Parents rate the frequency with which each parenting practice occurs in their home from "1=never" to "5=always." Higher scores indicate more positive parenting.

    Time frame: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.

07

Study locations

2 of 2 sites recruiting
  • UNC Pediatrics at Panther Creek
    Cary, North Carolina 27519, United States
    Recruiting
  • UNC Children's Primary and Specialty Care at Carolina Pointe II
    Chapel Hill, North Carolina 27517, United States
    Recruiting
    • Katherine Jordan, MD · Contactkatherine_jordan@med.unc.edu · (984) 974-6669
    • Yasamin Sanii, MD · Principal investigator
    • Samantha Schilling, MD, MSPH · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07303062
Responsible party
Sponsor
First posted
Dec 24, 2025
Start date
May 28, 2026
Primary completion
Mar 1, 2027 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
Sep 18, 2026

Study contacts

Samantha Schilling, MD MSHP
study director · University of North Carolina, Chapel Hill
Yasamin Sanii, MD
principal investigator · University of North Carolina, Chapel Hill

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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