Actively Recruiting

Phase Not Applicable
Age: 5Years - 18Years
All Genders
ID06934525

Testing Delivery of Modalities in Community Health Settings: Developing Pathways to Health Equity

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

501

Participants Needed

1

Research Sites

25 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

Researchers are evaluating different ways to deliver Cognitive Behavioral Therapy (CBT) for children and adolescents aged 5 to 18 who have anxiety disorders or obsessive-compulsive disorder (OCD). The study aims to find out which method of delivering CBT—either in-person, via telehealth, or a flexible mix of both—best increases access to treatment and improves outcomes. This research is conducted by the Pediatric Anxiety Research Center at Brown University Health and involves collaboration with several community care sites in Rhode Island to reach diverse youth populations. Participants will receive weekly CBT sessions focused on exposure therapy, which helps them gradually face feared situations. Treatment teams include a licensed provider once a month and an exposure coach three times a month. Participants are randomly assigned to one of three delivery methods: attending sessions entirely in-person, fully through remote video calls, or a flexible approach that combines both. The treatment takes place in community settings such as offices, homes, or via a secure video platform. During the study, participants will complete various assessments before starting treatment, during treatment at weeks 8 and 16, at the end of treatment, and at follow-ups 3 and 6 months after treatment ends. These assessments measure anxiety severity, OCD symptoms, satisfaction with treatment, disability, and barriers to care, among others. Weekly monitoring of exposure activities and homework compliance is also part of the study. Participants will be compensated for completing research assessments, and the total study duration includes treatment and follow-up periods.

CONDITIONS

Brief 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...

  • Age 5 to 18 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 available to participate in treatment
Not Eligible

You will not qualify if you...

  • Primary or co-primary psychiatric disorder requiring other active current treatment
  • Acute suicidality
  • Currently receiving psychotherapy
  • Chronic medical illness preventing active participation
  • Unstable psychotropic medication treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for eligibility assessment

Treatment

Duration - 24 weeks

Participants receive team-delivered, exposure-based cognitive behavioral therapy with licensed and non-licensed providers.

1 visit per month with licensed provider and 3 visits per month with non-licensed provider

Follow-up

Duration - Up to 12 months post-treatment

Participants are monitored after treatment completion to assess outcomes and satisfaction over time.

Visits at 6 months and 12 months post-treatment

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

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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