Obsessive Compulsive Disorder Clinical Trial
Official title:
fMRI Studies in Pathological Gambling and Obsessive-Compulsive Disorder
This study will explore the brain processes associated with inhibition and reward processing in pathological gamblers and people with obsessive compulsive disorder compared to healthy controls.
Status | Terminated |
Enrollment | 57 |
Est. completion date | December 2010 |
Est. primary completion date | December 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria: - Male or female adults diagnosed with pathological gambling or obsessive compulsive disorder aged 18-55. - Subject has signed an informed consent form - Must provide contact information - Must be in generally good health - Must be willing and able to read written instructions and complete scales - Must be English speaking - In the opinion of the investigator, the subject is capable of complying with all study procedures Pathological Gamblers only: - Current diagnosis of pathological gambling, supported by DSM-IV SCI-PG - Must score = 5 on SOGS - Must score = 2 on item number 1 on the G-SAS - Subjects must have a severity score of = 4 (moderately ill) on the Clinical Global Impressions Scale - Severity (CGI-S) - Must score = 10 on questions 1-5 on PG-Y-BOCS - Must score = 15 on YMRS - Must have gambled once within past 2 weeks of Screening Visit. Exclusion Criteria: - Subjects with a primary diagnosis of schizophrenia, personality disorder, or other psychotic disorders - Subjects with a primary diagnosis of an Axis I disorder that may require intervention - Must not score >24 on the Montgomery-Asberg Depression Rating Scale (MADRS) (pathological gamblers only) - Subjects who live in a restrictive environment - Subjects with a current DSM-IV diagnosis of substance dependence or abuse, excluding nicotine - Subjects reporting a history of drug and/or alcohol dependence or abuse; subjects who report occasional drug use in the past will be discussed by a panel (consisting of Dr. Gilbert, Dr. Fan and Dr. Bartz), and will be considered for participation on a case by case basis - Subjects who have used psychotropic medications in the past week to six weeks (depending on the medication) - Subject has a positive drug urine screen - Female subjects who are pregnant - Subjects who report a history of severe liver, heart, or kidney disease because these conditions are associated with neurological sequella - Employees of the investigator or study center or their families - Finally, subjects who do not satisfy the following criteria will be excluded because they will be unable to undergo the MRI procedure. Specifically, subjects will be excluded who have: 1. a pacemaker 2. any implanted metallic chips in their head 3. ever worked around a metal lathe or had a shrapnel (war or gun shot) wound/injury 4. an implanted neuro-stimulatory or infusion/insulin pump 5. any devices placed in their blood vessels 6. any metal in/on their body 7. kidney disease 8. sickle-cell or hemolytic anemia 9. claustrophobia 10. any metallic tattoos 11. any body piercing that cannot be removed 12. dental braces 13. any permanent make-up 14. any cardiac stints |
Observational Model: Case Control, Time Perspective: Cross-Sectional
Country | Name | City | State |
---|---|---|---|
United States | Mount Sinai School of Medicine | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Icahn School of Medicine at Mount Sinai | Abbott |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | fMRI - go-nogo task | a measure of behavioral response inhibition | at baseline | No |
Primary | fMRI - monetary incentive delay (MID) task | a measure of neural response to anticipating and receiving monetary rewards | at baseline | No |
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