- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00051233
Treatment of Schizophrenia Through Internet-Based Psychoeducation
Schizophrenia Patient and Family Continuity of Care
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study will provide a comprehensive psychoeducational program which includes education, social support, information, coping strategies, and guidance from mental health, social services, and medical professionals. This study will work to reduce relapse, facilitate patient rehabilitation, decrease family distress, and improve family well being.
Patients and their families participate in an in-person Psychoeducational Survival Skills Workshop that is designed to provide patients and their families with basic information about schizophrenia and its treatment. After the workshop, participants are provided with 6 Web-based modules that are designed to increase mental health and schizophrenia knowledge. Patient relapse, family distress, family knowledge of schizophrenia, and data on user's acceptance and utilization are measured to determine the intervention's effectiveness.
Study Type
Enrollment
Phase
- Phase 2
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15261
- University of Pittsburgh Western Psychiatric Institute and Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria
- DSM-IV diagnosis of schizophrenia or schizoaffective disorder
- At least 4 hours/week in-person contact with a family member
- Primary caregiver with a telephone
- Patient and primary caregiver speak and read English
Exclusion Criteria:
- Enrolled in another clinical trial
- Evidence of organic brain syndrome
- Current alcohol or substance abuse that could explain the presenting index psychotic episode
- DSM-IV diagnosis of psychoactive substance dependency
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Armando J Rotondi, University of Pittsburgh
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01MH063484 (U.S. NIH Grant/Contract)
- DSIR SE-DR
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.