Initial Development and Dissemination of OC-Go
OC-GoPhaseI
Facilitating Fidelity and Dissemination of Evidence Based Treatment for Childhood OCD Via an Interactive Crowd-sourced Patient-provider Tool
1 other identifier
observational
8
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started May 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 19, 2017
CompletedFirst Posted
Study publicly available on registry
April 24, 2017
CompletedStudy Start
First participant enrolled
May 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2018
CompletedNovember 18, 2020
November 1, 2020
12 months
April 19, 2017
November 16, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
System Usability Scale (SUS)
10-item self-report measure assessing the usability of the OC-Go application
6 weeks
Usability Evaluation for e-Learning Applications (UELA),
54-item self-report measure assessing the usability of the OC-Go application
6 weeks
Study Arms (1)
OC-Go
Approximately 10-20 9-17 year-olds receiving exposure based cognitive behavior therapy for OCD through the UCLA Division of Child and Adolescent Psychiatry OCD treatment programs
Interventions
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
Eligibility 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
You may qualify if:
- Children receiving exposure based CBT through the UCLA Child OCD, Anxiety and Tic Disorders Clinic or Pediatric OCD Intensive Outpatient Program and their parents
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of California, Los Angeleslead
- Virtually Better, Inc.collaborator
Study Sites (1)
Univ. of California / Los Angeles / Semel Inst.
Los Angeles, California, 90024-1759, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
John Piacentini, Ph.D.
University of California, Los Angeles
- PRINCIPAL INVESTIGATOR
Peter Tuerk, Ph.D.
Virtually Better, Inc.
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Psychiatry and Biobehavioral Sciences
Study Record Dates
First Submitted
April 19, 2017
First Posted
April 24, 2017
Study Start
May 1, 2017
Primary Completion
April 30, 2018
Study Completion
April 30, 2018
Last Updated
November 18, 2020
Record last verified: 2020-11
Data Sharing
- IPD Sharing
- Will not share