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CompletedNCT04701372Updated Jan 8, 2021

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

An observational study in Obsessive-Compulsive Disorder, sponsored by NOCD. Completed at 1 site in United States. Open to participants aged 10 Years and older. Per ClinicalTrials.gov, last updated 2021-01-08.

Sponsored by NOCD · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
2,069
Ages
10 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Obsessive-Compulsive Disorder

Keywords

  • exposure and response prevention
  • digital behavioral health
  • remote treatment
  • video therapy
03

In context

Compulsive Personality Disorder

367 studies on the registry are indexed under Compulsive Personality Disorder; 67 are open to participants now.

This study's enrollment of 2,069 is above the median of 102 across 41 observational studies indexed under Compulsive Personality Disorder.

Browse Compulsive Personality Disorder studies →

Lead sponsor

NOCD is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
10 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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.

Inclusion criteria

  • obsessive-compulsive disorder

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
2,069 participants (actual)
Patient registry
No

Groups and cohorts

  • Obsessive-Compulsive Disorder

    adults, adolescents, and children with obsessive-compulsive disorder

    Behavioral: Exposure and response prevention therapy

Interventions

  • BehavioralExposure and response prevention therapy

    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.

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What researchers measure

Primary outcomes

  1. Dimensional Obsessive-Compulsive Scale

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

    Time frame: change from pre-treatment to post-treatment (after 11 weeks)

Secondary outcomes

  1. Diagnostic Interview for Anxiety, Mood, and OCD and Related Neuropsychiatric Disorders (DIAMOND) OCD severity scale

    clinician-rated psychometric instrument to measure overall OCD symptom severity

    Time frame: pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

  2. Depression Anxiety and Stress Scale (DASS-21)

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

    Time frame: pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

  3. Quality of Life Enjoyment and Satisfaction Questionnaire -- Short Form (QLES-Q)

    self-rated psychometric instrument to measure quality of life

    Time frame: pre-treatment, after 4 weeks, and post-treatment (after 11 weeks)

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Study locations

1 site
  • Nocd, Llc
    Chicago, Illinois 60601, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04701372
Lead sponsor
NOCD
Responsible party
Sponsor
First posted
Jan 8, 2021
Start date
Jan 1, 2020
Primary completion
Nov 8, 2020
Completion
Nov 8, 2020
Last update
Jan 8, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

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