Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT05048251

Individually Targeted Neuromodulation for Contamination-based OCD

Led by Mclean Hospital · Updated on 2024-03-15

50

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

Sponsors

M

Mclean Hospital

Lead Sponsor

M

Massachusetts General Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Patients with obsessive-compulsive disorder (OCD) experience a wide array of different types of obsessions and compulsions. However, current treatments for OCD employ a "one size fits all" approach and are used for all patients regardless of symptom type. In this project, the investigators propose to investigate whether a novel method of transcranial magnetic stimulation specifically reduces contamination/washing symptoms - one of the most common types of OCD.

CONDITIONS

Official Title

Individually Targeted Neuromodulation for Contamination-based OCD

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female aged 18 to 55 years
  • Diagnosis of OCD as the primary disorder according to DSM-5
  • Contamination/washing is the predominant symptom dimension on the Dimensional Yale-Brown Obsessive Compulsive Scale (D-YBOCS)
  • Score of 8 or higher on the contamination dimension of the D-YBOCS
  • Not taking psychiatric medications or on a stable dose of SSRI, clomipramine, SNRI, or second generation antipsychotic for at least 4 weeks before enrollment
  • Use of PRN benzodiazepines allowed if dose and usage have been stable before enrollment
  • No medication changes allowed during the study
  • No new exposure and response prevention (ERP) therapy started within 4 weeks before enrollment
  • Ongoing ERP therapy allowed if started more than 8 weeks before enrollment
Not Eligible

You will not qualify if you...

  • Positive urine drug screen except for prescribed benzodiazepines
  • Use of psychiatric medications other than those permitted in the inclusion criteria
  • Substance use disorder within the last 3 months, except nicotine
  • History of schizophrenia, bipolar disorder, autism, or Tourette's syndrome
  • Active suicidal thoughts in the week before screening
  • History of traumatic brain injury, seizure disorder, neurodegenerative disease, or other organic brain disease
  • Pregnancy or currently breastfeeding
  • Contraindications for MRI scanning or transcranial magnetic stimulation (TMS)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

R

Rosalind Sokoll

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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