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Clinical Trials/NCT05580081
NCT05580081
Completed
N/A

Optimizing CBT Implementation Among Community Providers Through Internet-based Consultation and Networking (i-CAN)

University of Alabama, Tuscaloosa1 site in 1 country100 target enrollmentApril 1, 2023
ConditionsAnxietyCBT

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anxiety
Sponsor
University of Alabama, Tuscaloosa
Enrollment
100
Locations
1
Primary Endpoint
Reasoned Action Questionnaire
Status
Completed
Last Updated
last year

Overview

Brief Summary

Although anxiety is one of the most common and debilitating mental health conditions affecting children and adolescents, the vast majority of sufferers do not receive effective treatment. Cognitive-behavioral therapy (CBT) is an evidence-based, frontline treatment for pediatric anxiety, yet many community-based practitioners do not implement CBT with high fidelity, which can detrimentally affect its clinical impact. The goal of this study is to develop and test an online platform to support community providers' effective use of CBT for pediatric anxiety.

Detailed Description

Stemming from implementation science and, specifically, the Theory of Planned Behavior, investigators are working alongside community stakeholders to develop a novel, online consultation platform. This platform, termed Internet-based Consultation or Networking (or i-CAN) will utilize a professional navigator (i.e., a provider with CBT expertise), online support and resources, and parallel peer consultation to create a user-friendly and supportive community for providers to get support as they implement CBT. Once finalized, the platform will be tested in the context of a preliminary randomized controlled trial (RCT) with approximately 100 mental healthcare providers who work with anxious children and adolescents. Providers who enroll will be randomly assigned to either the experimental condition (i-CAN) or the control condition (wait-list for i-CAN). The primary outcome of interest is change in intentions to use CBT.

Registry
clinicaltrials.gov
Start Date
April 1, 2023
End Date
February 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Alabama, Tuscaloosa
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • provide direct mental healthcare to anxious youth
  • practice in general community within state of Alabama
  • agree to try i-CAN

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Reasoned Action Questionnaire

Time Frame: 18 weeks

Questionnaire that assesses instrumental beliefs, perceived norms, and self-efficacy (all related to use of cognitive-behavioral therapy). On the Reasoned Action Questionnaire, higher scores indicate greater intention to use the therapeutic approach. Scores can range from 14 to 90.

Secondary Outcomes

  • Evidence-based practice attitude scale(18 weeks)

Study Sites (1)

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