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Brief Hospitalization for Schizophrenia: Strategies to Improve Treatment Outcome

This study has been completed.
Information provided by:
VA Office of Research and Development Identifier:
First received: July 3, 2001
Last updated: January 20, 2009
Last verified: December 2004
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.

Condition Intervention
Schizophrenic Disorder
Behavioral: Community Re-Entry Program: What is Schizophrenia

Study Type: Interventional
Study Design: Intervention Model: Parallel Assignment
Official Title: Brief Hospitalization for Schizophrenia: Strategies to Improve Treatment Outcome

Resource links provided by NLM:

Further study details as provided by VA Office of Research and Development:

Study Start Date: April 1998
Estimated Study Completion Date: March 2001

Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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.
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Please refer to this study by its identifier: NCT00018837

United States, California
VA Greater Los Angeles Healthcare System
Los Angeles, California, United States, 90073
Sponsors and Collaborators
VA Office of Research and Development
  More Information Identifier: NCT00018837     History of Changes
Other Study ID Numbers: MHBS-010-98S
Study First Received: July 3, 2001
Last Updated: January 20, 2009

Additional relevant MeSH terms:
Schizophrenia Spectrum and Other Psychotic Disorders
Mental Disorders processed this record on May 22, 2017