Individually Targeted Neuromodulation for Contamination-based OCD

Description

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

Obsessive-Compulsive Disorder

Study Overview

Study Details

Study overview

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.

Individually Targeted Neuromodulation for Contamination-based Obsessive-compulsive Disorder

Individually Targeted Neuromodulation for Contamination-based OCD

Condition
Obsessive-Compulsive Disorder
Intervention / Treatment

-

Contacts and Locations

Belmont

McLean Hospital, Belmont, Massachusetts, United States, 02478

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. male or female age 18-55 years old
  • 2. DSM-5 diagnosis of OCD as primary presenting disorder
  • 3. CONTAM as the predominant symptom dimension (i.e., Dimension 4 (CONTAM symptoms) is the highest score on the Dimensional Yale-Brown Obsessive Compulsive Scale (D-YBOCS); participants with more than one Dimension as highest score will still be eligible as long as Dimension 4 is one of these)
  • 4. score of ≥ 8 on Dimension 4 of the D-YBOCS
  • 5. taking no psychiatric medications or on a stable dose of an SSRI, clomipramine, SNRI, or second generation antipsychotic for at least 4 weeks prior to enrollment. Use of PRN benzodiazepines will be permitted as long as the dose/usage has not changed significantly leading up to enrollment. No medication changes will be permitted during the study
  • 6. have not initiated a new course of exposure and response prevention (ERP) therapy within 4 weeks of enrollment (ongoing ERP will be permitted if initiated more than 8 weeks before enrollment).
  • 1. positive urine drug screen (other than prescribed benzodiazepines)
  • 2. use of psychiatric medications other than permitted above
  • 3. substance use disorder in the last 3 months (with the exception of nicotine)
  • 4. history of schizophrenia, bipolar disorder, autism, Tourette's syndrome (current and past history of depressive, anxiety, and eating disorders permitted as long as OCD is considered the primary disorder)
  • 5. active suicidal ideation over the week prior to screening (as indicated by answering yes to questions 1 or 2 on the C-SSRS)
  • 6. history of traumatic brain injury, seizure disorder, neurodegenerative disease, or other organic brain disease
  • 7. pregnancy or lactating
  • 8. contraindication to MRI scanning or TMS

Ages Eligible for Study

18 Years to 55 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mclean Hospital,

Brian P Brennan, MD, PRINCIPAL_INVESTIGATOR, Mclean Hospital

Study Record Dates

2024-06-30