Clinical Outcomes From NOCD Treatment of Obsessive-Compulsive Disorder Using Exposure and Response Prevention
Clinical Outcomes From NOCD Digital Behavioral Health Treatment of Obsessive-Compulsive Disorder Using Exposure and Response Prevention
1 other identifier
observational
2,069
1 country
1
Brief Summary
This is a naturalistic, observational study of individuals with obsessive-compulsive disorder who were treated with exposure and response prevention via video teletherapy, augmented with between-session support with text messaging and an online community forum.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2020
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
Study Start
First participant enrolled
January 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 8, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
November 8, 2020
CompletedFirst Submitted
Initial submission to the registry
January 2, 2021
CompletedFirst Posted
Study publicly available on registry
January 8, 2021
CompletedJanuary 8, 2021
January 1, 2021
10 months
January 2, 2021
January 7, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Dimensional Obsessive-Compulsive Scale
self-rated psychometric instrument to measure symptom severity of multiple OCD subtypes
change from pre-treatment to post-treatment (after 11 weeks)
Secondary Outcomes (3)
Diagnostic Interview for Anxiety, Mood, and OCD and Related Neuropsychiatric Disorders (DIAMOND) OCD severity scale
pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)
Depression Anxiety and Stress Scale (DASS-21)
pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)
Quality of Life Enjoyment and Satisfaction Questionnaire -- Short Form (QLES-Q)
pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)
Study Arms (1)
Obsessive-Compulsive Disorder
adults, adolescents, and children with obsessive-compulsive disorder
Interventions
Exposures and response prevention therapy (a type of cognitive-behavioral therapy for obsessive-compulsive disorder), delivered in real-time by licensed therapists remotely via video. The treatment was augmented by between-session text messaging and online community support.
Eligibility Criteria
This is a naturalistic sample of children, adolescents, and adults with obsessive-compulsive disorder (OCD) who sought treatment for OCD from NOCD, LLC, a digital behavioral health company.
You may qualify if:
- obsessive-compulsive disorder
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- NOCDlead
Study Sites (1)
Nocd, Llc
Chicago, Illinois, 60601, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 2, 2021
First Posted
January 8, 2021
Study Start
January 1, 2020
Primary Completion
November 8, 2020
Study Completion
November 8, 2020
Last Updated
January 8, 2021
Record last verified: 2021-01