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OpenTrials
Completed

NCT Number: NCT03126305

Initial Development and Dissemination of OC-Go

The clinical component of Phase I application development examines the clinical utility, feasibility, and functionality of the OC-Go application via an 8-month pilot trial consisting of 50 standard CBT sessions augmented with OC-Go in OCD-diagnosed children who are receiving treatment through the pediatric OCD treatment programs in the UCLA Division of Child and Adolescent Psychiatry

Completed

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Key information

Conditions

Obsessive-Compulsive Disorder Anxiety Disorders Mental Disorders

Age range

9 year–17 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Univ. of California / Los Angeles / Semel Inst.

Los Angeles, California, 90024-1759, United States

About this study

This project seeks to refine and assess OC-Go, a HIPAA-compliant web-based clinician portal and patient-side mobile application designed to increase patient adherence to evidence-based treatment (EBT) for Obsessive Compulsive Disorder (OCD), a common and impairing condition, and provider ability to effectively implement EBTs. OC-Go allows clinicians to create and push tailored assignments to patients on their mobile devices with an optimized user interface that includes patient accountability and support features. Accordingly, patients can be guided to do assignments by themselves between sessions with increased fidelity over the course of treatment. Once therapy assignments are created and shared to a crowd-sourced and curated public library, any clinician can assign any task to any patient for homework or in-session use with one touch. Use of OC-Go is expected to increase patient engagement, compliance, treatment efficiency, dissemination of EBTs, and therapist confidence and expertise.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children receiving exposure based CBT through the UCLA Child OCD, Anxiety and Tic Disorders Clinic or Pediatric OCD Intensive Outpatient Program and their parents

Exclusion criteria

  • None

Treatment and study plan

OC-Go

Other

OC-Go, a HIPAA-compliant web-based clinician portal and patient-side mobile application that allows clinicians to create and push tailored treatment assignments to patients on their mobile devices

Primary outcomes

  1. System Usability Scale (SUS)

    Time frame: 6 weeks

    10-item self-report measure assessing the usability of the OC-Go application

  2. Usability Evaluation for e-Learning Applications (UELA),

    Time frame: 6 weeks

    54-item self-report measure assessing the usability of the OC-Go application

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • Virtually Better, Inc.

Registry information

Official study title

Facilitating Fidelity and Dissemination of Evidence Based Treatment for Childhood OCD Via an Interactive Crowd-sourced Patient-provider Tool

Acronym: OC-GoPhaseI

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 24, 2017
Registry last updated
Nov 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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