Pilot Study of CBT With tDCS for Adults Being Treated for Obsessive Compulsive Disorder

Rogers Behavioral Health

Status: Withdrawn

Conditions: Obsessive-Compulsive Disorder

Treatments: Device: Sham transcranial direct current stimulation; Device: transcranial direct current stimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT05964998

22-ROGE-103

Details and patient eligibility

About

This pilot study aims to compare the effect of transcranial direct current stimulation (tDCS) versus sham stimulation, delivered immediately prior to cognitive-behavioral therapy (CBT) for obsessive-compulsive disorder (OCD), on patient-reported outcomes. The investigator hypothesize that patients who receive active stimulation will experience greater improvement in OCD symptoms than those who receive sham stimulation.

Sex: All

Ages: 18 to 55 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Primary diagnosis of Obsessive-Compulsive Disorder (OCD)
• Resident of state of Wisconsin
• Enrolled in OCD Intensive Outpatient Program (IOP) at Rogers Behavioral Health in Oconomowoc, WI
• Ability to communicate effectively using written and spoken English

Exclusion criteria

• Metal in the body of any kind (e.g., braces, pacemakers, metal plates or screws, intracranial electrodes, implanted devices/defibrillators, prostheses)
• Currently taking medication that reduces seizure threshold (e.g., clomipramine)
• Cranial pathologies (e.g., holes, plates)
• History of seizure or black-out concussion
• Pregnancy
• Previous treatment at Rogers Behavioral Health

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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0 participants in 2 patient groups

Active stimulation

Experimental group

Treatment:

Device: transcranial direct current stimulation

Sham stimulation

Sham Comparator group

Treatment:

Device: Sham transcranial direct current stimulation