Obsessive-Compulsive Disorder (OCD) Clinical Trial
Official title:
Cognitive-Behavioral Therapy and Glutamate in Cingulate Gyrus in OCD
Verified date | March 2020 |
Source | University of California, Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Even with the best available treatments for obsessive-compulsive disorder (OCD), most patients only partially recover and many patients do not respond at all. Such incomplete and inadequate response contributes to greater public health costs in terms of morbidity and patient care expenses. This study aims for a better understanding of abnormal brain chemistry in OCD and how it is affected by cognitive-behavioral therapy (CBT) in order to develop novel therapies and improve the success of existing therapies. The main hypothesis is that CBT will change levels of the excitatory neurotransmitter glutamate in OCD patients in a region of the brain involved in OCD known as the cingulate cortex.
Status | Completed |
Enrollment | 75 |
Est. completion date | June 2015 |
Est. primary completion date | June 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - meets DSM-IV-TR diagnostic criteria for OCD as primary (most severe) diagnosis based on Anxiety Disorders Interview Schedule (ADIS) Clinical Severity Rating - reported DSM-IV-TR-threshold OCD symptom onset age 18 or later - Yale-Brown Obsessive-Compulsive total score greater than or equal to 16 - fluent English speaker - signed informed consent Exclusion Criteria: - IQ of less than 80 on the Wechsler Abbreviated Scales of Intelligence - lifetime DSM-IV diagnosis of pervasive developmental disorder, mania, psychosis, conduct disorder, or substance dependence assessed through ADIS - current DSM-IV diagnosis of major depressive disorder if ADIS CSR rating is 4 or higher (severe) or attention-deficit hyperactivity disorder - primary compulsive hoarding - any changes (dose or agent) in psychotropic medication for OCD or other psychiatric condition within 12 weeks prior to enrollment - severe illness that requires immediate inpatient psychiatric intervention - any serious psychiatric, psychosocial, or neurological condition requiring immediate treatment other than that provided in the current study - any body metal (other than dental fillings), positive pregnancy test, or other MR scan contraindications - prior trial of CBT for OCD, regardless of outcome - medical conditions that affect cerebral metabolism (e.g., thyroid disorders or diabetes) |
Country | Name | City | State |
---|---|---|---|
United States | UCLA Obsessive-Compulsive Disorder Intensive Treatment Program | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Los Angeles | National Institute of Mental Health (NIMH) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | MRSI glutamate | Regional concentration of glutamate in brain, as measured by magnetic resonance spectroscopic imaging (MRSI) | 4 weeks | |
Secondary | Y-BOCS | Severity of core obsessive-compulsive clinical symptoms as measured with the Yale-Brown Obsessive-Compulsive Scale score | 4 weeks |
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