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Clinical Trials/NCT01885923
NCT01885923
Unknown
Not Applicable

Prospective, Randomized, Open, Controlled Study With Information and Telecommunication Technology-aided Relapse Prevention Program in Schizophrenia.

Prague Psychiatric Center1 site in 1 country150 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Relapse Schizophrenia
Sponsor
Prague Psychiatric Center
Enrollment
150
Locations
1
Primary Endpoint
Primary Objective: The hospitalization-free survival rate at 18 months in active group compared to the control group.
Last Updated
12 years ago

Overview

Brief Summary

THE AIM OF THE PROJECT The main aim lies in the prevention of frequent relapses typical for schizophrenia and schizoaffective disorder by means of simple, highly cost-effective information technology-aided approach RESEARCH HYPOTHESIS A the end of 18 months study duration, patients in the active group enrolled in ITAREPS will demonstrate statistically significantly reduced risk of hospitalization, decreased number of hospitalization days and reduced direct inpatient costs in comparison to control group not using the program.

Detailed Description

The ITAREPS 2.0 program employs telecommunication and information technologies in order to detect fluctuations in longitudinal mental health status of patient with schizophrenia and thus signalize the very early stages of prodromes preceding relapse. This approach opens an avenue towards early pharmacological intervention. Subjects (150 patients with diagnosis of schizophrenia and schizoaffective disorder and their family members) will be randomized at a 1:1 ratio into the active or control group. Participants from the active group will be completing two separate versions of the 10-item Early Warning Signs Questionnaire (EWSQ) upon a weekly SMS request generated automatically by the system during 18 months study duration. In this group, automatically generated e-mail alert message feedback to the investigator will be activated in case of prodrome detection, prompting investigator to antipsychotic dose increase by 20%. The control (treatment-as-usual) group will not use ITAREPS system.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
December 2015
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Filip Spaniel, M.D., Ph.D

MD

Prague Psychiatric Center

Eligibility Criteria

Inclusion Criteria

  • For entry into the study, the following criteria MUST be met:
  • Men and women, ages 18 to 60 years, inclusive.
  • A diagnosis of schizophrenia or schizoaffective disorder according to ICD-10 classification.
  • Having at least TWO psychiatric hospitalization for psychosis before the study enrollment.
  • Severity (CGI-S) ≤ 3 at study Visit
  • All patients must be on stable doses of antipsychotic medication during the study entry.

Exclusion Criteria

  • Organic mental disorder,
  • mental disorder due to psychoactive substance use or mental retardation.
  • Participation in another relapse prevention program.
  • Hayward compliance rating scale score \< 2 at Visit 1.

Outcomes

Primary Outcomes

Primary Objective: The hospitalization-free survival rate at 18 months in active group compared to the control group.

Time Frame: 18 months

Secondary Outcomes

  • Number of psychiatric hospitalization days(18months)
  • Direct impatient costs(18months)
  • Direct cost of outpatient antipsychotic medication(18months)
  • Cumulative exposition to antipsychotic medication in both active ITAREPS and control groups(18months)

Study Sites (1)

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