Actively Recruiting

Phase Not Applicable
Age: 6Years - 17Years
All Genders
Healthy Volunteers
NCT06104904

Managing Anxiety in Pediatric Primary Care (MAPP)

Led by UConn Health · Updated on 2024-12-09

60

Participants Needed

1

Research Sites

114 weeks

Total Duration

On this page

Sponsors

U

UConn Health

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to conduct a randomized controlled trial to enhance the capacity of pediatric primary care providers to assist their patients who struggle with anxiety. The study aims to refine and assess the feasibility of the Anxiety Action Plan (AxAP), a brief intervention to reduce pediatric anxiety, delivered by primary care providers (PCPs) in community pediatric primary care clinics. The goal of the AxAP is to enhance the capacity of PCPs to identify and intervene with anxious youth, which will enhance access to care in general and especially in locations with few mental health specialists. PCPs participating in this study will attend a training, administer the intervention to enrolled youth assigned to the MAPP condition, participate in coaching sessions, and fill out study questionnaires. Families participating in this study will complete evaluations with the study team, receive the intervention from their PCP (if assigned to the MAPP condition), and fill out study questionnaires. Researchers will compare the MAPP intervention to Enhanced Usual Care (EUC; consisting of videos, handouts, and other resources for anxiety reduction) to see the differences, if any, in child outcomes.

CONDITIONS

Official Title

Managing Anxiety in Pediatric Primary Care (MAPP)

Who Can Participate

Age: 6Years - 17Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth aged 6 to 17 years
  • Elevated anxiety symptoms with a Screen for Child Anxiety Rated Disorders score between 20 and 55 (parent or child report)
  • Primary care providers must have a PA, RN, NP, APRN, or MD degree
  • Primary care providers must work at least part time in a primary care setting
Not Eligible

You will not qualify if you...

  • Youth with medical or psychiatric conditions that contraindicate participation, including suicidality
  • Youth currently receiving psychosocial mental health treatment for anxiety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UConn Health

West Hartford, Connecticut, United States, 06119

Actively Recruiting

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Research Team

G

Golda S Ginsburg, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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