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Psychosocial Therapy and Risperidone Treatment in Work Performance in Recent-Onset Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Cognitive remediation training (CT)
Healthy behavior training (HBT)
Risperidone, administered orally (Oral Ris)
Risperidone, administered via injection (RLAI)
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Schizoaffective Disorder, Depressed Type, Schizophreniform Disorder, First-Episode Schizophrenia, Supported Employment, Cognitive Remediation, Health Behavior Training, Antipsychotic Medication

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

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 intelligence quotient (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

Sites / Locations

  • Semel Institute for Neuroscience and Human Behavior at UCLA

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Cog Remediation, risperidone injection

Healthy Behavior Training, risperidone injection

Cog Remediation, oral risperidone

Healthy Behavior Training, oral risperidone

Arm Description

Participants will receive cognitive remediation training plus risperidone, administered via injection.

Participants will receive health behavior training plus risperidone, administered via injection.

Participants will receive cognitive remediation training plus risperidone administered orally.

Participants will receive health behavior training plus risperidone administered orally.

Outcomes

Primary Outcome Measures

Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB)
Values presented here are the changes in MCCB Overall Composite T scores from baseline to 12 months, with higher values representing better outcome. Raw test scores are used to generate T-scores and then the seven MCCB domains are combined to generate an Overall Composite T score. MCCB Overall Composite T scores have a mean in the general population of 50 with a standard deviation of 10. Thus, a positive change of 5 T scores is an improvement of half a standard deviation.
Work/School Functioning (Global Functioning Scale: Role)
Change in role functioning from baseline to the 6 month point (rated on a scale from 1= Extreme Role Dysfunction to 10 = Superior Role Functioning) is presented here.
Average Medication Non-adherence
5-point scale (1 = best adherence, 5= nonadherent) based on pill counts, Medication Event Monitoring System (MEMS) cap readings, plasma assays, and psychiatrist judgements for oral risperidone and timing of injections for long-acting injectable risperidone. Averaged over medication study participation.
Work/School Functioning (Global Functioning Scale: Role)
Changes in role functioning from baseline to 12 months. Ratings on a 10-point scale with 10 being best.

Secondary Outcome Measures

Work Behavior Inventory (WBI) Quality of Work/School Performance
Change in rating on quality of work/school performance based on patient, employer, and/or teacher reports. The Quality of Work rating at baseline was subtracted from the same rating at 12 mos. Higher scores are better outcome.
Maintenance of Work/School Attendance
Modified Work Section of the Social Adjustment Scale (SAS) was used to calculate the total number of weeks in school or competitive work. Range of possible values is 0 to 52, with higher numbers being better outcome.
Exacerbation or Relapse of Psychotic Symptoms
Dichotomous measure: Presence of any of 3 psychotic relapse or exacerbation categories scored from the Brief Psychiatric Rating Scale (BPRS) occurring after randomization and until end of study participation (up to 12 months post baseline). BPRS was administered every two weeks throughout study participation.
Retention in Treatment
Days after randomization that a participant continued to receive at least the assigned CT or HBT psychosocial treatment. If a participant needed to end the assigned medication condition (RLAI vs. Oral Ris), they continued in the psychosocial treatment so this outcome focused on the days in the assigned psychosocial treatment. Possible range is 1 to 365, with higher being a better outcome.
Awareness of Illness, as Assessed by the Scale to Assess Unawareness of Mental Disorder, Revised Version (SUMD-R)
Rating scale based on clinician's interview of patient to determine level of lack of awareness of having a mental disorder. Range is from 1 (Aware) to 5 (Unaware), so lower scores indicate better outcome.
Change in Motivation for Work/School
The Work Motivation scale is a factor score from the Work Personality Profile. The Work Personality Profile is a set of ratings based on interviewing the participant. Scores at each occasion can range from 8 to 32, with higher indicating better motivation. Scores reported here are changes from baseline to 12 months, which could range from -24 to 24 with higher being better.
Change in Coping Strategies
Coping Response Inventory, which rates extent to which active coping strategies were used after a significant stressful life event. Range of possible scores is 1 to 4. Higher scores are better.

Full Information

First Posted
June 1, 2006
Last Updated
March 4, 2020
Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH), Janssen Scientific Affairs, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00333177
Brief Title
Psychosocial Therapy and Risperidone Treatment in Work Performance in Recent-Onset Schizophrenia
Official Title
Developmental Processes in Schizophrenic Disorders: Cognitive Remediation, Medication Adherence, and Work Outcome in Recent-Onset Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH), Janssen Scientific Affairs, LLC

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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 once 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizoaffective Disorder, Depressed Type, Schizophreniform Disorder, First-Episode Schizophrenia, Supported Employment, Cognitive Remediation, Health Behavior Training, Antipsychotic Medication

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cog Remediation, risperidone injection
Arm Type
Experimental
Arm Description
Participants will receive cognitive remediation training plus risperidone, administered via injection.
Arm Title
Healthy Behavior Training, risperidone injection
Arm Type
Active Comparator
Arm Description
Participants will receive health behavior training plus risperidone, administered via injection.
Arm Title
Cog Remediation, oral risperidone
Arm Type
Experimental
Arm Description
Participants will receive cognitive remediation training plus risperidone administered orally.
Arm Title
Healthy Behavior Training, oral risperidone
Arm Type
Active Comparator
Arm Description
Participants will receive health behavior training plus risperidone administered orally.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive remediation training (CT)
Intervention Description
Cognitive remediation training includes computerized cognitive training plus learning skills group.
Intervention Type
Behavioral
Intervention Name(s)
Healthy behavior training (HBT)
Intervention Description
Healthy behavior training includes group skills training in nutrition, exercise, and relaxation.
Intervention Type
Drug
Intervention Name(s)
Risperidone, administered orally (Oral Ris)
Other Intervention Name(s)
Risperdal
Intervention Description
Oral risperidone at dosage judged optimal by treating psychiatrist
Intervention Type
Drug
Intervention Name(s)
Risperidone, administered via injection (RLAI)
Other Intervention Name(s)
Risperdal Consta
Intervention Description
Risperidone in injectable form every 2 weeks, starting with 25 mg and adjusted as needed
Primary Outcome Measure Information:
Title
Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB)
Description
Values presented here are the changes in MCCB Overall Composite T scores from baseline to 12 months, with higher values representing better outcome. Raw test scores are used to generate T-scores and then the seven MCCB domains are combined to generate an Overall Composite T score. MCCB Overall Composite T scores have a mean in the general population of 50 with a standard deviation of 10. Thus, a positive change of 5 T scores is an improvement of half a standard deviation.
Time Frame
Measured at baseline and 12 months
Title
Work/School Functioning (Global Functioning Scale: Role)
Description
Change in role functioning from baseline to the 6 month point (rated on a scale from 1= Extreme Role Dysfunction to 10 = Superior Role Functioning) is presented here.
Time Frame
Baseline to 6 months
Title
Average Medication Non-adherence
Description
5-point scale (1 = best adherence, 5= nonadherent) based on pill counts, Medication Event Monitoring System (MEMS) cap readings, plasma assays, and psychiatrist judgements for oral risperidone and timing of injections for long-acting injectable risperidone. Averaged over medication study participation.
Time Frame
Averaged over study participation (up to 12 months)
Title
Work/School Functioning (Global Functioning Scale: Role)
Description
Changes in role functioning from baseline to 12 months. Ratings on a 10-point scale with 10 being best.
Time Frame
Baseline to 12 months
Secondary Outcome Measure Information:
Title
Work Behavior Inventory (WBI) Quality of Work/School Performance
Description
Change in rating on quality of work/school performance based on patient, employer, and/or teacher reports. The Quality of Work rating at baseline was subtracted from the same rating at 12 mos. Higher scores are better outcome.
Time Frame
Baseline to 1 year
Title
Maintenance of Work/School Attendance
Description
Modified Work Section of the Social Adjustment Scale (SAS) was used to calculate the total number of weeks in school or competitive work. Range of possible values is 0 to 52, with higher numbers being better outcome.
Time Frame
12 months
Title
Exacerbation or Relapse of Psychotic Symptoms
Description
Dichotomous measure: Presence of any of 3 psychotic relapse or exacerbation categories scored from the Brief Psychiatric Rating Scale (BPRS) occurring after randomization and until end of study participation (up to 12 months post baseline). BPRS was administered every two weeks throughout study participation.
Time Frame
Occurence after randomization and until end of study participation (up to 12 mos.)
Title
Retention in Treatment
Description
Days after randomization that a participant continued to receive at least the assigned CT or HBT psychosocial treatment. If a participant needed to end the assigned medication condition (RLAI vs. Oral Ris), they continued in the psychosocial treatment so this outcome focused on the days in the assigned psychosocial treatment. Possible range is 1 to 365, with higher being a better outcome.
Time Frame
12 months
Title
Awareness of Illness, as Assessed by the Scale to Assess Unawareness of Mental Disorder, Revised Version (SUMD-R)
Description
Rating scale based on clinician's interview of patient to determine level of lack of awareness of having a mental disorder. Range is from 1 (Aware) to 5 (Unaware), so lower scores indicate better outcome.
Time Frame
12 months after randomization
Title
Change in Motivation for Work/School
Description
The Work Motivation scale is a factor score from the Work Personality Profile. The Work Personality Profile is a set of ratings based on interviewing the participant. Scores at each occasion can range from 8 to 32, with higher indicating better motivation. Scores reported here are changes from baseline to 12 months, which could range from -24 to 24 with higher being better.
Time Frame
Baseline to 12 months
Title
Change in Coping Strategies
Description
Coping Response Inventory, which rates extent to which active coping strategies were used after a significant stressful life event. Range of possible scores is 1 to 4. Higher scores are better.
Time Frame
Baseline to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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 intelligence quotient (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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keith H. Nuechterlein, PhD
Organizational Affiliation
University of California, Los Angeles, Department of Psychiatry and Biobehavioral Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Semel Institute for Neuroscience and Human Behavior at UCLA
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32981534
Citation
Nuechterlein KH, Ventura J, Subotnik KL, Gretchen-Doorly D, Turner LR, Casaus LR, Luo J, Boucher ML, Hayata JN, Bell MD, Medalia A. A randomized controlled trial of cognitive remediation and long-acting injectable risperidone after a first episode of schizophrenia: improving cognition and work/school functioning. Psychol Med. 2022 Jun;52(8):1517-1526. doi: 10.1017/S0033291720003335. Epub 2020 Sep 28.
Results Reference
derived
PubMed Identifier
26107752
Citation
Subotnik KL, Casaus LR, Ventura J, Luo JS, Hellemann GS, Gretchen-Doorly D, Marder S, Nuechterlein KH. Long-Acting Injectable Risperidone for Relapse Prevention and Control of Breakthrough Symptoms After a Recent First Episode of Schizophrenia. A Randomized Clinical Trial. JAMA Psychiatry. 2015 Aug;72(8):822-9. doi: 10.1001/jamapsychiatry.2015.0270.
Results Reference
derived

Learn more about this trial

Psychosocial Therapy and Risperidone Treatment in Work Performance in Recent-Onset Schizophrenia

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