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NCT00448331 Clinical Trial

Facilitated Referral for Children Screening Positive for Mental Illness

Mental Disorders Clinical Trial

— MI  

Official title:
Facilitated Referral for Children Screening Positive for Mental Illness in the Pediatric Emergency Department and Readiness to Seek Care

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00448331
Other study ID # 02-9-27
Secondary ID MH063916-03
Status Completed
Phase Phase 0
First received March 14, 2007
Last updated October 31, 2007
Start date June 2004
Est. completion date August 2007

Study information
Verified date October 2007
Source Children's Hospital Medical Center, Cincinnati
Contact n/a
Is FDA regulated No
Health authority United States: National Institutes of Health (NIH)
Study type Observational

Clinical Trial Summary

The purpose of this study is to find out how prevalent unidentified Mental Health issues are in the pediatric population that visits the Emergency Department in an urban city.

Description:

The purpose of this research study is to find out how many children in the Emergency Room have emotional issues and how many of them go unnoticed. In particular the study looks at how well a questionnaire for children and teenagers, the DISC Predictive Scales, Version IV (DPS-IV) works and what is the best way to ask the questions. In addition, for children aged 9-17 this study will look at families' readiness to seek care when a problem is indicated.

Recruitment information / eligibility
Status Completed
Enrollment 551
Est. completion date August 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 6 Years to 18 Years
Eligibility Inclusion Criteria:

- Child Must be With Biological Mother

- Child Presenting to Emergency Department with an Urgent But Stable condition

- Child must be between the ages of 6 years and 18 years

- Child must have no prior history of Behavioral Health concerns or diagnoses

Exclusion Criteria:

- Child has prior Behavioral Health history, diagnosis, or concerns

- Child not between ages of 6 years and 18 years of ages

- Child presenting without Biological Mother present

- Child acuity level outside of Urgent But Stable for presenting complaints

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Cincinnati Children's Hospital Medical Center Emergency Department Cincinnati Ohio

Sponsors (2)
Lead Sponsor Collaborator
Children's Hospital Medical Center, Cincinnati National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

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