Improving Care and Reducing Cost Study
NCT02364544 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 461
Last updated 2017-03-23
Summary
The goal of the Improving Care and Reducing Cost (ICRC) Program, is to improve disease management and the overall process of care in treating the chronic illness schizophrenia in order to reduce ER visits and hospital days while providing better care, better health and increased patient satisfaction. This will be done by fostering innovation in the use of technology and by training and deploying a new cadre of personnel in the behavioral health field: Mental Health/Health Technology (MH/HT) Case Managers.
Conditions
- Schizophrenia
- Schizoaffective Disorder
- Psychosis NOS
Interventions
- BEHAVIORAL
-
Relapse Prevention Plan
brief, in-person, relapse prevention counseling with supplemental web-based learning modules,
- BEHAVIORAL
-
Daily Support Website
web-based program for patients and families that provides psychoeducation about schizophrenia and its treatments to improve knowledge, increase problem-solving skills and offer social support through the use of web-based therapist facilitated sessions
- BEHAVIORAL
-
Computer CBT for voices and paranoia
A ten-session CBT programs, one to address voices and the other for paranoia. The web-based programs incorporate the essential elements of CBT for psychosis such as normalizing behavior and offering behavioral coping strategies
- BEHAVIORAL
-
FOCUS
an interactive smart phone text-messaging application to support medication adherence, facilitate coping with symptoms and improve daily functioning in individuals with schizophrenia
- OTHER
-
Prescriber Decision Assistant
is a web-based prescriber decision support system that includes a brief patient-completed assessment describing symptoms and adverse events which prompts the prescriber to conduct a detailed clinical assessment. Embedded in the program are decision supports for medication choices based on best evidence-based practices regarding symptoms, side effects, information from laboratory tests and history of prior treatment response
Sponsors & Collaborators
-
University of Pittsburgh
collaborator OTHER -
Boston University
collaborator OTHER -
Dartmouth-Hitchcock Medical Center
collaborator OTHER -
Northwell Health
lead OTHER
Principal Investigators
-
John Kane · Northwell Health
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-04-30
- Primary Completion
- 2015-06-30
- Completion
- 2015-06-30
Countries
- United States
Study Locations
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