Actively Recruiting

Phase Not Applicable
Age: 5Years - 18Years
All Genders
NCT06934525

Implementing Team-Based Treatment for Pediatric Anxiety in Community Mental Health Settings

Led by Bradley Hospital · Updated on 2026-05-14

501

Participants Needed

1

Research Sites

195 weeks

Total Duration

On this page

Sponsors

B

Bradley Hospital

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to test how the delivery of Cognitive Behavioral Therapy (CBT) for pediatric anxiety and OCD via different methods might increase its availability and effectiveness. CBT involves teaching the patient skills to enable them to gradually come into contact with feared situations. This process of gradually approaching feared situations is called exposure. Although CBT with exposure has the best evidence for treating anxiety disorders, not all children have equal access or respond the same way to CBT. As part of this study, patients will receive weekly CBT treatment sessions involving a combination of weekly visits with an exposure coach and one visit a month with a licensed provider (e.g., psychologist, social worker). This treatment will be delivered using one of three methods: 1) in-person (face-to-face sessions, occurring in the office and the home/community), or 2) telehealth (entirely remote sessions via web-based video conference), or 3) flexible (individualized mix of in-person and/or telehealth sessions). Eligible participants will be randomly assigned to one of these three methods. Results of this study will help determine which treatment method works best for whom. Treatment as described above will occur as part of care at partnering community care sites in Rhode Island. Providers from the following partnering community care sites will make up patient treatment teams: Blackstone Valley Community Health Care, Family Services of Rhode Island, Gateway Healthcare, Newport Mental Health, and Thrive Behavioral Health. The research study is being conducted by the Pediatric Anxiety Research Center at Brown University Health. The research team will conduct the study assessments that patients will be asked to participate in as study participants. Patients will be asked to complete assessments prior to starting treatment, at two time points during treatment, at the end of treatment, and at two timepoints 3 and 6 months following the end of treatment. Participants will be compensated for their time completing research assessments.

CONDITIONS

Official Title

Implementing Team-Based Treatment for Pediatric Anxiety in Community Mental Health Settings

Who Can Participate

Age: 5Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 5 to 18 years inclusive
  • Primary or co-primary DSM-V diagnosis of anxiety or OCD
  • Symptoms present for at least 3 months
  • Requires outpatient care
  • Has a stable parent or guardian who can participate in treatment
Not Eligible

You will not qualify if you...

  • Has another primary psychiatric disorder needing new active treatment
  • Experiencing acute suicidality
  • Currently receiving psychotherapy
  • Has a chronic medical illness preventing active treatment participation
  • Taking psychotropic medication that is not stable

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

Bradley Hospital

East Providence, Rhode Island, United States, 02915

Actively Recruiting

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Research Team

J

Jennifer Freeman, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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