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Recruiting NCT04373629

NCT04373629 Perceptual Abnormalities and Their Malleability in BDD

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Clinical Trial Summary
NCT ID NCT04373629
Status Recruiting
Phase
Sponsor Centre for Addiction and Mental Health
Condition Body Dysmorphic Disorder
Study Type INTERVENTIONAL
Enrollment 146 participants
Start Date 2020-12-01
Primary Completion 2025-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 40 Years
Study Type INTERVENTIONAL
Interventions
attentional modulationperceptual modulationnaturalistic viewing

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 146 participants in total. It began in 2020-12-01 with a primary completion date of 2025-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

A core symptom of body dysmorphic disorder (BDD) is perceptual distortions for appearance, which contributes to poor insight and delusionality, limits engagement in treatment, and puts individuals at risk for relapse. Results from this study will provide a comprehensive mechanistic model of brain, behavioral, and emotional contributors to abnormal perceptual processing, as well as how malleable it is with visual modulation techniques. This will lay the groundwork for next-step translational perceptual retraining approaches.

Eligibility Criteria

Inclusion Criteria: Body dysmorphic disorder: Inclusion: * males or females * ages 18-40 * meet Diagnostic and Statistical Manual-5 (DSM-5) criteria for Body Dysmorphic Disorder * have a Body Dysmorphic Disorder version of the Yale-Brown Obsessive-Compulsive Disorder Scale (BDD-YBOCS) score of ≥20 * primary appearance concerns of the face or head area * medication naïve or medication free for at least 8 weeks prior to enrollment Inclusion Criteria: Subclinical body dysmorphic disorder: Inclusion: * males or females * ages 18-40 * have a score on the Dysmorphic Concern Questionnaire of ≥8 \[1 standard deviation (STD) above population norms\] - primary appearance concerns of the face or head area * medication naïve or medication free for at least 8 weeks prior to enrollment Inclusion Criteria: Healthy controls: Inclusion * Healthy males and females from any racial or ethnic background - ages 18-40 * have a score on the Dysmorphic Concern Questionnaire of \<8 Exclusion Criteria: Body dysmorphic disorder: Exclusion * concurrent major Axis I disorders including substance use disorders, aside from anxiety disorders or depressive disorders, as these comorbidities are very common and the sample would otherwise be non-representative; however BDD must be the primary diagnosis. * lifetime: bipolar disorder or psychotic disorder. * psychotropic medications, aside from a short half-life sedative/hypnotic for insomnia, or a short half-life benzodiazepine as needed for anxiety but not exceeding a frequency of 3 doses in one week and not to be taken on the days of the training or MRI scan * current cognitive-behavioral therapy Exclusion: Subclinical body dysmorphic disorder: Exclusion * meet full DSM-5 criteria for Body Dysmorphic Disorder * current Axis I disorders including substance use disorders * lifetime: bipolar disorder or psychotic disorder * psychotropic medications, aside from a short half-life sedative/hypnotic for insomnia, or a short half-life benzodiazepine as needed for anxiety but not exceeding a frequency of 3 doses in one week and not to be taken on the days of the training or MRI scan * current cognitive-behavioral therapy Exclusion Criteria: Healthy Controls: Exclusion * Any current Axis I disorder * lifetime: bipolar disorder or psychotic disorder * Psychiatric medication Exclusion Criteria: All participants: Exclusion * Neurological disorder * Pregnancy * Current major medical disorders that may affect cerebral metabolism such as diabetes or thyroid disorders - Current risk of suicide with a plan and intent * Ferromagnetic metal implantations or devices (electronic implants or devices, infusion pumps, aneurysm clips, metal fragments or foreign bodies, metal prostheses, joints, rods or plates) * Visual acuity worse than 20/35 for each eye as determined by Snellen close vision acuity chart (vision will be tested with corrective lenses if participant uses them).

Contact & Investigator

Central Contact

Research Analyst

✉ bdd.research@camh.ca

📞 (416) 535-8501

Principal Investigator

Jamie D Feusner, M.D.

PRINCIPAL INVESTIGATOR

Centre for Addiction and Mental Health

Frequently Asked Questions

Who can join the NCT04373629 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 40 Years, studying Body Dysmorphic Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04373629 currently recruiting?

Yes, NCT04373629 is actively recruiting participants. Contact the research team at bdd.research@camh.ca for enrollment information.

Where is the NCT04373629 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT04373629 clinical trial?

NCT04373629 is sponsored by Centre for Addiction and Mental Health. The principal investigator is Jamie D Feusner, M.D. at Centre for Addiction and Mental Health. The trial plans to enroll 146 participants.

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