Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05224414

Interpretation Bias as a Mechanism of Treatment Response in OCD

Led by Mclean Hospital · Updated on 2025-05-08

106

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will conduct a randomized controlled trial of Cognitive Bias Modification for Interpretation (CBM-I) as an augmentation to treatment as usual for obsessive compulsive disorder (OCD). CBM-I is a digital intervention designed to directly manipulate interpretation bias through repeated practice on a training task, thereby inducing cognitive changes in a relatively automatic or implicit manner. Specifically, this study will examine the feasibility, acceptability, and clinical outcomes associated with CBM-I. Adults with obsessive compulsive disorder (OCD) will be recruited from a treatment program for this disorder and participants will be randomly assigned to either receive: 1) up to 12 sessions of CBM-I, or or up to 12 sessions of psychoeducation as a control condition.

CONDITIONS

Official Title

Interpretation Bias as a Mechanism of Treatment Response in OCD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (over 18 years old) who are patients at the OCD Institute
  • Able to complete a computer task lasting 20 minutes
  • Consent to participate in the main OCD Institute study protocol
  • Primary diagnosis of OCD confirmed by clinical diagnosis and a Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score above 16
  • Score above 131 on the Obsessive Beliefs Questionnaire-44 at admission
Not Eligible

You will not qualify if you...

  • Currently experiencing acute symptoms of psychosis
  • Diagnosis of a psychotic disorder

AI-Screening

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Trial Site Locations

Total: 1 location

1

McLean Hospital

Belmont, Massachusetts, United States, 02478

Actively Recruiting

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Research Team

M

Martha Falkenstein, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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