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Clinical Trials/NCT02364544
NCT02364544
Completed
Not Applicable

The Improving Care and Reducing Cost (ICRC) Program

Northwell Health8 sites in 1 country461 target enrollmentApril 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
Northwell Health
Enrollment
461
Locations
8
Primary Endpoint
Total Number of Hospitalization and Emergency Room Visits
Status
Completed
Last Updated
9 years ago

Overview

Brief 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.

Detailed Description

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. The specific treatments we propose to use are evidence based, but their dissemination has been limited because of lack of trained personnel and cost. The model we propose, the Health Technology Program (HTP), will address these problems through use of the web and mobile phone based training and interventions. The components of the HTP program that are being tested in the pilot program include: 1) evidence-based pharmacological treatment facilitated by a web-based prescriber decision support system-Prescriber Decision Assistant (PDA) 2) brief, in-person, relapse prevention counseling with supplemental web-based learning modules, 3) a daily support website that offers web- and phone-based resources to support persons with schizophrenia and their family members or others. The resources include a patient and family Psycho-Education Treatment program, which includes electronic peer groups facilitated by mental health professionals, providing medication reminders via web and phone, and conducting monitoring of early warning signs of relapse via web and phone 4) an interactive smart phone text-messaging application to support medication adherence, facilitate coping with symptoms and improve daily functioning in individuals with schizophrenia 5) a web-based, self-administered cognitive-behavioral therapy (CBT) program for the management of hallucinations. All patients will be provided with pharmacological treatment (PDA), brief in-person relapse prevention counseling, and an Android mobile phone. The other program components will be provided to patients using a shared decision-making approach to assess need and preference.

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
June 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John Kane

Senior Vice President, Behavioral Health Services

Northwell Health

Eligibility Criteria

Inclusion Criteria

  • • Age 18 to 60, (patients age 51-60 require review from the coordinating site)
  • Clinical diagnosis of:
  • schizophrenia
  • schizoaffective disorder
  • psychosis NOS
  • Has had two or more inpatient hospitalizations for treatment of a psychotic disorder
  • Currently in the hospital or up to 30 days of inpatient hospitalization for a psychotic disorder
  • o If patients are sent to a partial, or day hospital following an inpatient hospitalization, the 30 day window begins at the time of discharge from the day or partial hospital
  • Any ethnicity
  • Ability to participate in research assessments in English

Exclusion Criteria

  • • Individuals who cannot understand what research participation entails, or correctly answer the questions about research participation that are part of the Study Information Review and provide fully informed consent will be excluded
  • More than 30 days since discharge from a psychiatric hospitalization
  • Any other serious medical condition that in the opinion of the investigator would seriously impair functioning making the patient unsuitable for the trial
  • Patients who would likely find it burdensome and/or have difficulty sustaining the use of a laptop computer and /or smart phone due to issues of security, consistent connectivity or other factors.

Outcomes

Primary Outcomes

Total Number of Hospitalization and Emergency Room Visits

Time Frame: Baseline, Month 1, Month2, Month 3, Month4, Month 5, and Month 6

Captures the number of hospital and ER visits each month

Secondary Outcomes

  • Service Utilization Resource Form(Baseline, month 3, month 6)
  • Change from Baseline Heinrich's Quality of Life Scale(Baseline and month 6)

Study Sites (8)

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