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Recovery Guide Intervention for Recurrent Psychiatric Hospitalization
This study is currently recruiting participants.
Verified by Yale University, March 2009
First Received: November 15, 2006   Last Updated: March 2, 2009   History of Changes
Sponsors and Collaborators: Yale University
Connecticut State, Department of Mental Health and Addiction Services
Eli Lilly and Company
Information provided by: Yale University
ClinicalTrials.gov Identifier: NCT00400166
  Purpose

The purpose of this study is to determine whether Recovery Guide support services are effective in promoting recovery and social integration among psychiatrically disabled individuals who experience high rates of inpatient hospitalizations.


Condition Intervention
Schizophrenia
Schizoaffective Disorder
Bipolar Disorder
Psychotic Depression
Behavioral: Recovery Mentor

MedlinePlus related topics: Bipolar Disorder Depression Psychotic Disorders Schizophrenia
U.S. FDA Resources
Study Type: Interventional
Study Design: Supportive Care, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study
Official Title: Recovery Guide Intervention for Recurrent Psychiatric Hospitalization

Further study details as provided by Yale University:

Primary Outcome Measures:
  • Number of hospitalizations [ Time Frame: 3 and 9 months ] [ Designated as safety issue: No ]
  • Number of treatment contacts [ Time Frame: 3 and 9 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Sense of community [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]
  • Motivation for change [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]
  • Social functioning [ Time Frame: Baseline, 3 abd 9 months ] [ Designated as safety issue: No ]
  • Hope [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]
  • Self-determination [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]
  • Functional status [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]
  • Treatment relationship [ Time Frame: Baseline, 3 and 9 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 120
Study Start Date: December 2006
Estimated Study Completion Date: April 2009
Estimated Primary Completion Date: April 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Recovery Mentor
Behavioral: Recovery Mentor
Provided Recovery Mentor services
0: No Intervention
No Recovery Mentor, services as usual

Detailed Description:

The paradigm shift in mental health treatment from a deficit-and institution- based framework to a recovery and community integration frame necessitates new models of "case management" practices. The Recovery Guide model is just such a model. Beyond theoretical frameworks, the effectiveness of Recovery Guides has not been well studied. It is the intent of this study to conduct a randomized trial examining the effects of Recovery Guides on community tenure and integration. Furthermore, it is the intent of this study to to establish fidelity criteria.

Comparison(s): Recovery Guide services in addition to treatment as usual, compared to treatment as usual.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 18 years of age or older
  • Currently admitted in the Yale-New Haven Psychiatric Hospital (YNHPH)
  • A history of two or more prior admissions within the past 18 months
  • Proficient in the use of the English language
  • A DSM-IV diagnosis of Schizophrenia, Schizoaffective Disorder, Psychotic Disorder NOS, or Major Depressive Disorder with Psychotic Features

Exclusion Criteria:

  • Inability to give signed, written consent
  • Primary DSM-IV diagnosis of substance abuse/dependence
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00400166

Contacts
Contact: Dave Sells, PhD 203-764-8691 david.sells@yale.edu
Contact: Larry Davidson, PhD 203-764-7583 larry.davidson@yale.edu

Locations
United States, Connecticut
Yale-New Haven Psychiatric Hospital Recruiting
New Haven, Connecticut, United States, 06519
Principal Investigator: William H Sledge, MD            
Sponsors and Collaborators
Yale University
Connecticut State, Department of Mental Health and Addiction Services
Eli Lilly and Company
Investigators
Principal Investigator: William H Sledge, MD Yale University
  More Information

Additional Information:
No publications provided

Responsible Party: Yale University School of Medicine ( William H. Sledge, M.D.; Director, Yale Psychiatric Hospital; Chair, Yale Department of Psychiatry; George D & Esther S Gross Professor of Psychiatry )
Study ID Numbers: 0607001641
Study First Received: November 15, 2006
Last Updated: March 2, 2009
ClinicalTrials.gov Identifier: NCT00400166     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Yale University:
Peer support
Psychiatric disability
Mutual support
Psychiatric Rehabilitation

Study placed in the following topic categories:
Schizophrenia
Affective Disorders, Psychotic
Depression
Mental Disorders
Bipolar Disorder
Mood Disorders
Psychotic Disorders
Depressive Disorder, Major
Depressive Disorder
Schizophrenia and Disorders with Psychotic Features
Recurrence
Behavioral Symptoms

Additional relevant MeSH terms:
Depression
Disease
Bipolar Disorder
Depressive Disorder, Major
Depressive Disorder
Behavioral Symptoms
Schizophrenia
Affective Disorders, Psychotic
Pathologic Processes
Mental Disorders
Mood Disorders
Psychotic Disorders
Schizophrenia and Disorders with Psychotic Features

ClinicalTrials.gov processed this record on May 06, 2009