Emergency Linkage to Outpatient Psychiatric Services

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00278811
Recruitment Status : Completed
First Posted : January 18, 2006
Last Update Posted : October 22, 2015
National Institute of Mental Health (NIMH)
Information provided by (Responsible Party):
Glenn Currier, University of Rochester

Brief Summary:
The purpose of this study is to compare two different kinds of follow-up care and their effects on psychiatric service use and psychological well-being. This randomized, controlled trial of subjects discharged from the psychiatric emergency services to outpatient care receive traditional hospital-based outpatient clinic referrals (treatment as usual) or appointments for community-based follow-up by a mobile crisis team.

Condition or disease Intervention/treatment Phase
Emergency Services, Psychiatric Procedure: mobile crisis team Phase 1

Detailed Description:
There are subgroups of patients who only seek care in emergency settings. An effective strategy to link that group to ambulatory care involves extending contact with psychiatric emergency services beyond the initial hospital-based visit. The "window of opportunity" to promote successful treatment linkage is brief. This is a study of a novel treatment format that seeks to expand the concept of the emergency contact, the study patients method of entering the mental health system of care, and by doing this, enhance retention in prescribed outpatient care. The effects of the intervention on patient symptoms and mental health service use will be examined.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 120 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: Emergency Linkage to Outpatient Psychiatric Services
Study Start Date : April 2003
Actual Primary Completion Date : March 2006
Actual Study Completion Date : March 2006

Primary Outcome Measures :
  1. Subjects randomized to the experimental treatment will demonstrate significantly increased rates of linkage to first outpatient contact as compared with subjects randomized to control treatment. [ Time Frame: 1 week ]

Secondary Outcome Measures :
  1. Subjects randomized to experimental treatment will demonstrate significantly reduced levels of psychiatric symptoms and significantly increased scores of overall functioning at 3 months after study enrollment, [ Time Frame: 3 months ]
  2. and will demonstrate significantly higher use of outpatient mental health clinical services, lower use of ED contacts, and lower use of inpatient mental health services versus the control group during the six months after study enrollment. [ Time Frame: 3 months ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • English and Spanish-speaking adult patients (18-and above) presenting to the psychiatric emergency service who rate a "1" or higher on the Spectrum of Suicidal Behavior of Pfeffer screening scale, and who have outpatient followup organized by Comprehensive Psychiatric Emergency Program staff through hospital outpatient psychiatric services are eligible for inclusion.

Exclusion Criteria:

  • Subjects less than 18 years old, those rated as not suicidal in the emergency department, subjects with mental retardation/developmental delay, and subjects who have community psychiatric treatment that they elect to continue in lieu of hospital outpatient psychiatric services referral are ineligible.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00278811

United States, New York
University of Rochester Medical Center
Rochester, New York, United States, 14642
Sponsors and Collaborators
University of Rochester
National Institute of Mental Health (NIMH)
Principal Investigator: Glenn W. Currier, M.D., M.P.H. University of Rochester

Responsible Party: Glenn Currier, Professor, University of Rochester Identifier: NCT00278811     History of Changes
Other Study ID Numbers: 09541
First Posted: January 18, 2006    Key Record Dates
Last Update Posted: October 22, 2015
Last Verified: October 2015

Keywords provided by Glenn Currier, University of Rochester:
Mental Health Services
Suicide ideation

Additional relevant MeSH terms:
Disease Attributes
Pathologic Processes