Psychosocial Therapy and Risperidone Treatment in Work Performance in Recent-Onset Schizophrenia
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Purpose
This study will determine the effectiveness of various combinations of psychosocial therapy and risperidone treatment in improving work or school performance in people with first-episode schizophrenia.
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia |
Behavioral: Cognitive remediation Behavioral: Health behavior training Drug: Risperidone, administered orally Drug: Risperidone, administered via injection Behavioral: Individual Placement and Support |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Developmental Processes in Schizophrenic Disorders: Cognitive Remediation, Medication Adherence, and Work Outcome in Recent-Onset Schizophrenia |
- Cognitive performance on test battery (Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) battery plus additional measures) [ Time Frame: Measured at Months 6 and 12 ] [ Designated as safety issue: No ]
- Work or school functioning (Global Functioning Scale: Role) [ Time Frame: Measured every 3 months for 1 year ] [ Designated as safety issue: No ]
- Maintenance of work/school attendance (SAS) [ Time Frame: Measured every 3 months for 1 year ] [ Designated as safety issue: No ]
- Quality of work or school functioning, as assessed by the Work Behavior Inventory (WBI) [ Time Frame: Measured every 2 months for 1 year ] [ Designated as safety issue: No ]
- Medication adherence [ Time Frame: Measured every 2 weeks for 1 year ] [ Designated as safety issue: No ]
- Measured over 12 months: Exacerbation or relapse of psychotic symptoms, as assessed by the Brief Psychiatric Rating Scale (BPRS) [ Time Frame: Every 2 weeks ] [ Designated as safety issue: No ]
- Retention in treatment [ Time Frame: Every 3 months ] [ Designated as safety issue: No ]
- Awareness of illness, as assessed by the Scale to Assess Unawareness of Mental Disorder, Revised Version (SUMD-R) [ Time Frame: Every 6 months ] [ Designated as safety issue: No ]
- Increased motivation for work/school [ Time Frame: Every 6 months ] [ Designated as safety issue: No ]
- Improved coping strategies [ Time Frame: Every 6 months ] [ Designated as safety issue: No ]
| Enrollment: | 153 |
| Study Start Date: | March 2006 |
| Study Completion Date: | January 2013 |
| Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Participants will receive cognitive remediation training plus injectable, long-acting risperidone.
|
Behavioral: Cognitive remediation
Cognitive remediation training includes computerized cognitive training plus learning skills group.
Drug: Risperidone, administered via injection
Risperidone in injectable form every 2 weeks, starting with 25 mg and adjusted as needed
Other Name: Risperdal Consta
Behavioral: Individual Placement and Support
Supported education/employment
|
|
Active Comparator: 2
Participants will receive health behavior training plus injectable, long-acting risperidone.
|
Behavioral: Health behavior training
Health behavior training includes group skills training in nutrition, exercise, and relaxation.
Drug: Risperidone, administered via injection
Risperidone in injectable form every 2 weeks, starting with 25 mg and adjusted as needed
Other Name: Risperdal Consta
Behavioral: Individual Placement and Support
Supported education/employment
|
|
Experimental: 3
Participants will receive cognitive remediation training plus risperidone administered orally.
|
Behavioral: Cognitive remediation
Cognitive remediation training includes computerized cognitive training plus learning skills group.
Drug: Risperidone, administered orally
Oral risperidone at dosage judged optimal by treating psychiatrist
Other Name: Risperdal
Behavioral: Individual Placement and Support
Supported education/employment
|
|
Active Comparator: 4
Participants will receive health behavior training plus risperidone administered orally.
|
Behavioral: Health behavior training
Health behavior training includes group skills training in nutrition, exercise, and relaxation.
Drug: Risperidone, administered orally
Oral risperidone at dosage judged optimal by treating psychiatrist
Other Name: Risperdal
Behavioral: Individual Placement and Support
Supported education/employment
|
Detailed Description:
Schizophrenia is a chronic, severe, and disabling brain disorder. People with schizophrenia often experience hallucinations, delusions, thought disorders, and movement disorders. These symptoms make it difficult to maintain a job, participate in school, and keep up self-care. Proper treatment of first-episode schizophrenia may increase the chances of controlling disease progression on a long-term basis. Antipsychotic medications, such as risperidone, and psychosocial treatments, such as cognitive enhancement training and health behavior training, are common, effective treatments for schizophrenia. This study will determine the effectiveness of various combinations of psychosocial therapy and risperidone treatment in improving work or school performance in people with first-episode schizophrenia.
Participants in this open label study will be randomly assigned to receive one of the following four combinations of an antipsychotic medication and a psychosocial treatment: cognitive enhancement training plus oral risperidone; cognitive enhancement training plus long-acting injectable risperidone; health behavior training plus oral risperidone; or health behavior training plus long-acting injectable risperidone. Cognitive enhancement training will entail 2 hours per week of computer-assisted training targeted at improving attention, memory, and problem-solving skills. Additionally, participants will attend a weekly 1-hour group meeting to learn how to apply these skills to work and school situations. Health behavior training will involve 3 hours per week of relaxation training, nutrition education, and physical exercise to enhance wellness. Participants assigned to receive oral risperidone will receive their medication in pill form at the dosage determined to be optimal by the study psychiatrist. Participants assigned to receive injectable risperidone will be given one injection every 2 weeks. Dosages will start at 25 mg per injection and will be adjusted as needed.
Treatment will continue for 1 year following dosage stabilization, which typically occurs 2 to 3 months following study entry. For the first 6 months, participants assigned to receive health behavior training will attend study visits once a week and participants assigned to receive cognitive enhancement training will attend study visits twice a week. For the final 6 months, all participants will attend study visits twice weekly. At each visit, participants will receive their assigned psychosocial treatment; attend group therapy; meet with a case manager for counseling and assessment of symptoms, work functioning, and social functioning; and meet with a psychiatrist to monitor medication response. Additional cognitive and health behavior measures will be taken every 6 months to assess treatment effectiveness.
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Diagnosis of schizophrenia, schizoaffective disorder (depressed type), or schizophreniform disorder
- First major episode of psychotic symptoms occurred within 2 years prior to study entry
Exclusion Criteria:
- Neurological disorder or injury (e.g., encephalitis, epilepsy, traumatic brain injury)
- Mental retardation (e.g., premorbid IQ less than 70)
- Significant alcohol or substance use during last 6 months
- Unable to complete research measures in English
- Any condition that may make risperidone use medically inadvisable
Contacts and Locations| United States, California | |
| Semel Institute for Neuroscience and Human Behavior at UCLA | |
| Los Angeles, California, United States, 90095 | |
| Principal Investigator: | Keith H. Nuechterlein, PhD | University of California, Los Angeles, Department of Psychiatry and Biobehavioral Sciences |
More Information
No publications provided
| Responsible Party: | Keith Nuechterlein, Ph.D., Prinicipal Investigator, University of California, Los Angeles |
| ClinicalTrials.gov Identifier: | NCT00333177 History of Changes |
| Other Study ID Numbers: | R01 MH037705-06, R01MH037705, DAHBR AD-P |
| Study First Received: | June 1, 2006 |
| Last Updated: | March 27, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of California, Los Angeles:
|
Schizoaffective Disorder, Depressed Type Schizophreniform Disorder First-Episode Schizophrenia Supported Employment |
Cognitive Remediation Health Behavior Training Antipsychotic Medication |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders Risperidone Serotonin Antagonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions |
Physiological Effects of Drugs Antipsychotic Agents Tranquilizing Agents Central Nervous System Depressants Central Nervous System Agents Therapeutic Uses Psychotropic Drugs Dopamine Antagonists Dopamine Agents |
ClinicalTrials.gov processed this record on May 16, 2013