Relation of Catechol-O-methyltransferase (COMT) Genotype and Response to Cognitive Remediation Schizophrenia
Recruitment status was Recruiting
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Purpose
This project will explore the relationship between catechol-O-methyltransferase (COMT) Val158/108Met genotype and response to a 12-week computerized neurocognitive rehabilitation (CRT) given to chronic schizophrenic patients.
| Condition | Intervention |
|---|---|
|
Chronic Schizophrenia |
Behavioral: Cognitive remediation therapy Genetic: COMT Genotyping |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Basic Science |
| Official Title: | COMT Genotype and Response to Cognitive Remediation in Schizophrenia |
- To evaluate the effect of the association of COMT Val108/158 Met genotype with the response to a computerized neurocognitive rehabilitation treatment in patients with chronic schizophrenia. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- To expand the response to a computerized neurocognitive rehabilitation treatment in patients with chronic schizophrenia to other haplotypes or identified genes. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- To assess the differences in demographic variables (e.g. ethnicity, intellectual functioning as measured by WRAT III Reading test, and age) with response to computerized neurocognitive rehabilitation treatment in patients with chronic schizophrenia. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- To assess the differences between antipsychotic treatment and response to computerized neurocognitive rehabilitation treatment in patients with chronic schizophrenia. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 142 |
| Study Start Date: | April 2007 |
| Estimated Primary Completion Date: | April 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| CRT Group |
Behavioral: Cognitive remediation therapy
36 sessions of Computerized Cognitive Skills Training, 3 per week for 12 weeks.
Other Name: educational and behavioral training techniques
Genetic: COMT Genotyping
One time saliva sample is taken to genotype catechol-O-methyltransferase Val158/108Met alleles.
Other Names:
|
Detailed Description:
Cognitive deficits play a crucial role in both the pathogenesis and prognosis of schizophrenia. The COMT gene is functionally expressed in neural systems considered important in a range of healthy brain functions and brain disorders, including schizophrenia. The COMT Met allele has been shown to be associated with a lower activity form of COMT, and with better performance on neurocognitive tests, while the COMT Val allele is associated with poorer executive cognition. This study will investigate the relationship of COMT polymorphism in patients with chronic schizophrenia with the response to CRT targeting visuospatial processing, attention, and cognitive flexibility using MATRICS Consensus Cognitive Battery (MCCB) developed by the NIH-MATRICS initiative.
Eligibility| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Participation in the active arm of the neurocognitive remediation program
- Age 18 - 55
- Inpatients
- DSM-IV diagnosis of schizophrenia (all subtypes) with illness duration >5 years
- Auditory and visual acuity adequate to complete cognitive tests
- Stable dose of oral atypical antipsychotic for at least 4 weeks
- Total PANSS score > 60
- RBANS total score ≤ 80
- MMSE score of greater than or equal to 24
- Good physical health determined by physical examination, laboratory tests
- Capacity and willingness to give written informed consent
Exclusion Criteria:
- Inability to read or speak English
- Documented disease of the central nervous system
- History of intellectual impairment pre-dating onset of symptoms of psychosis (e.g. mental retardation)
- Clinically significant or unstable cardiovascular, renal, hepatic, gastrointestinal, pulmonary or hematologic conditions
- HIV +
- Patients diagnosed with substance dependence
- Currently participating in another experimental study, except for the parent study.
Contacts and Locations| Contact: Saurabh Kaushik, M.D. | 646-672-6352 | maisskk@omh.state.ny.us |
| Contact: Sashank Kaushik, M.D. |
| United States, New York | |
| Manhattan Psychiatric Center | Recruiting |
| Wards Island, New York, United States, 10035 | |
| Contact: Anzalee Khan, PhD marcakk@omh.state.ny.us | |
| Contact: Sashank Kaushik, M.D. | |
| Principal Investigator: | Jean-Pierre Lindenmayer, M.D. | Manhattan Psychiatric Center |
| Study Chair: | Saurabh Kaushik, M.D. | Manhattan Psychiatric Center |
| Study Chair: | Herbert Lachman, M.D. | Albert Einstein College of Medicine of Yeshiva University |
| Study Chair: | Susan Mc Gurk, PhD | New Hampshire-Dartmouth Psychiatric Research Center |
| Study Chair: | Anzalee Khan, PhD | Manhattan Psychiatric Center |
More Information
Additional Information:
Publications:
| Responsible Party: | Jean Pierre Lindenmayer, MC, Manhattan Psychiatric Center |
| ClinicalTrials.gov Identifier: | NCT00664274 History of Changes |
| Other Study ID Numbers: | 061/C39-0, 1R03MH078098-01 |
| Study First Received: | January 10, 2008 |
| Last Updated: | June 13, 2011 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders |
ClinicalTrials.gov processed this record on May 19, 2013