Actively Recruiting
Improving Mood for Adolescents Through Teaming With End-Users in Routine Care (The iMATTER Project)
Led by Children's Hospital of Philadelphia · Updated on 2025-06-15
45
Participants Needed
1
Research Sites
62 weeks
Total Duration
On this page
Sponsors
C
Children's Hospital of Philadelphia
Lead Sponsor
T
The Klingenstein Third Generation Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
This pilot randomized controlled trial will examine the feasibility, acceptability and preliminary efficacy of an adolescent depression prevention program, Brief Interpersonal Psychotherapy-Adolescent Skills Training (B-IPT-AST), in primary care.
CONDITIONS
Official Title
Improving Mood for Adolescents Through Teaming With End-Users in Routine Care (The iMATTER Project)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents aged 13 to 17 years
- English-speaking adolescents
- Legal guardian permission (informed consent) and child assent/consent
- Score of 5-10 on the Patient Health Questionnaire 9-Item: Modified for Teens (PHQ-9-M) during primary care well-visit
- Access to a phone, computer, or electronic device for study activities
- Legal guardian of an eligible adolescent aged 13 to 17 years
- Legal guardian consents to participate
- Legal guardian is English-speaking
- Legal guardian has access to phone, computer, or tablet for remote evaluations
You will not qualify if you...
- Suicidal thoughts or behaviors reported on PHQ-9-M at well-visit or baseline (including serious thoughts about ending life or prior suicide attempts)
- Major medical illness, significant behavioral problems, or intellectual/developmental disabilities interfering with study procedures
- Cases where medical record, screening, or family interactions indicate group program is inappropriate
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States, 19146
Actively Recruiting
Research Team
M
Molly F Davis, PhD
CONTACT
J
Jami F. Young, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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