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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00018837
Other study ID # MHBS-010-98S
Secondary ID
Status Completed
Phase N/A
First received July 3, 2001
Last updated January 20, 2009
Start date April 1998
Est. completion date March 2001

Study information

Verified date December 2004
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The goal of this research program is to implement a series of psychoeducational training classes designed to teach individuals with schizophrenia the importance of medication treatment, how to identify and manage medication side effects, and how to make appointments and emergency plans. The skills taught to the research subjects will lead to demonstrable increases (compared to the control group) in adherence to both the prescribed medication regimen and scheduled outpatient appointments and thereby cause a decrease (again compared to the control group) in rehospitalization rates and bed-days during subsequent twelve months following the intervention. A secondary objective of this work is that if the CREP program is successful and/or illness education is effective, the data will be able to disseminated throughout the VISN 22 via the recently awarded Mental Illness Research Education and Clinical Center (MIRECC) program.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date March 2001
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. Age 18-65 years of age.

2. DSM IV diagnosis of schizophrenia or schizoaffective disorder.

3. Competent to give informed consent.

4. Previously participated in "Brief Hospitalization for Schizophrenia: Strategies to Improve Treatment Outcome" Principal Investigator. Donna Wirshing, M.D.

Exclusion Criteria:

1. Physical or cognitive impairment of such severity as to adversely affect the validity of clinical ratings or impair capacity to give informed consent.

2. History of substantial substance dependence 6 months prior to the study.

3. Patients at high risk of suicide or other directed violence.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment


Related Conditions & MeSH terms


Intervention

Behavioral:
Community Re-Entry Program: What is Schizophrenia


Locations

Country Name City State
United States VA Greater Los Angeles Healthcare System Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

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