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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00750412
Other study ID # CCHMC 2008-0987
Secondary ID
Status Completed
Phase N/A
First received September 9, 2008
Last updated October 17, 2011
Start date March 2009
Est. completion date June 2010

Study information

Verified date October 2011
Source Children's Hospital Medical Center, Cincinnati
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the TeenScreen intervention to usual care for adolescents who screen positive for mental health problems in a pediatric emergency department. It is anticipated that adolescents receiving the TeenScreen intervention will be more likely to attend a first session of outpatient mental health services within 60 days of the initial screening than those receiving the usual care.


Recruitment information / eligibility

Status Completed
Enrollment 112
Est. completion date June 2010
Est. primary completion date June 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 11 Years to 17 Years
Eligibility Inclusion Criteria:

- Patients between 11 and 17 years old

- Medically stable and presenting with a non-psychiatric complaint

- English speaking

- Parent/guardian present for consent

- Insurance coverage by Medicaid

- Hamilton County residents

- Not currently receiving mental health treatment

Exclusion Criteria:

- Less than 11 years or greater than 17 years old

- Parent/guardian not present at time of visit

- Medically unstable

- Non-English speaking

- Insurance other than Medicaid

- Presenting complaint is a mental health problem

- Currently receiving mental health treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
TeenScreen Program
Adolescents who are randomized into the TeenScreen program and their parent/guardian will receive post-screening information, a facilitated referral, and case management services from a research social worker.

Locations

Country Name City State
United States Cincinnati Children's Hospital Medical Center Division of Emergency Medicine Cincinnati Ohio

Sponsors (2)

Lead Sponsor Collaborator
Children's Hospital Medical Center, Cincinnati Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Verified mental health service use through clinical administrative data 60 days after the initial mental health screening No
Secondary Measurement of depressive symptoms and impairment of functioning utilizing the Center for Epidemiological Studies-Depressions Scale and Sheehan Disability Score 60 days after the initial mental health screening No
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