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Clinical Outcomes From NOCD Treatment of Obsessive-Compulsive Disorder Using Exposure and Response Prevention

Completed
Conditions
Obsessive-Compulsive Disorder
Interventions
Behavioral: Exposure and response prevention therapy
Registration Number
NCT04701372
Lead Sponsor
NOCD
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
2069
Inclusion Criteria
  • obsessive-compulsive disorder
Exclusion Criteria
  • none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Obsessive-Compulsive DisorderExposure and response prevention therapyadults, adolescents, and children with obsessive-compulsive disorder
Primary Outcome Measures
NameTimeMethod
Dimensional Obsessive-Compulsive Scalechange from pre-treatment to post-treatment (after 11 weeks)

self-rated psychometric instrument to measure symptom severity of multiple OCD subtypes

Secondary Outcome Measures
NameTimeMethod
Diagnostic Interview for Anxiety, Mood, and OCD and Related Neuropsychiatric Disorders (DIAMOND) OCD severity scalepre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

clinician-rated psychometric instrument to measure overall OCD symptom severity

Depression Anxiety and Stress Scale (DASS-21)pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

self-rated psychometric instrument to measure depression, anxiety, and stress

Quality of Life Enjoyment and Satisfaction Questionnaire -- Short Form (QLES-Q)pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

self-rated psychometric instrument to measure quality of life

Trial Locations

Locations (1)

Nocd, Llc

🇺🇸

Chicago, Illinois, United States

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