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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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2 November 2015 |
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Main ID: |
NCT00278811 |
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Date of registration:
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16/01/2006 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Emergency Linkage to Outpatient Psychiatric Services
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Scientific title:
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Emergency Linkage to Outpatient Psychiatric Services |
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Date of first enrolment:
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April 2003 |
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Target sample size:
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120 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT00278811 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
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Phase:
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Phase 1
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Countries of recruitment
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United States
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Contacts
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Name:
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Glenn W. Currier, M.D., M.P.H. |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Rochester |
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Key inclusion & exclusion criteria
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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.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Emergency Services, Psychiatric
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Intervention(s)
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Procedure: mobile crisis team
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Primary Outcome(s)
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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]
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Secondary Outcome(s)
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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]
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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]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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