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Primary Care Based Depression Prevention for Adolescents/Young Adults/Young Adults and Young Adults - Article


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Wellness Screening: Young Adults

 




Clinical Trial: Primary Care Based Depression Prevention for Adolescents/Young Adults/Young Adults and Young Adults

This study is not yet open for patient recruitment.
Verified by University of Chicago September 2005

Sponsors and Collaborators: University of Chicago
NARSAD - National Alliance for Research on Schizopherenia and Depression
Information provided by: University of Chicago
ClinicalTrials.gov Identifier: NCT00145912

Purpose

The purpose of this research is to evaluate the feasibility of an interview between an adolescent / young adult and a PCP (Primary Care Physician).
Condition
Depression

MedlinePlus related topics:  Depression

Study Type: Observational
Study Design: Psychosocial, Longitudinal, Case Control, Prospective Study

Further Study Details: 

Expected Total Enrollment:  60

Study start: September 2005;  Expected completion: December 2007
Last follow-up: September 2005;  Data entry closure: December 2007

A web-based depression prevention program will evaluate the interview. Depression is a condition where people feel sad, tired, have changes in sleep, and lose interest in fun things for more than two weeks. This program teaches adolescents/young adults new skills. They learn new skills by talking with their doctor and doing a workbook at an Internet site. Counselors have used some of these lessons to successfully treat, and in some cases, prevent depression. We do not know if these lessons given in a primary care doctor’s office or over the Internet will prevent depression. We will have to do further studies to determine this. If subjects are clinically depressed right now, they cannot be a part of this study.

Eligibility

Ages Eligible for Study:  15 Years   -   21 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • (1) age 15-21 years and (2) two risk factors for developing depression in the next two years: Center for Epidemiologic Studies-Depression (CES-D) score > 12 and either a family history or past personal history of depression. Exclusion criteria include meeting criteria or undergoing active treatment for M. depression, or having suicidal ideation

Exclusion Criteria:

  • (1) undergoing active treatment for M. depression, or having suicidal ideation

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00145912

Benjamin W. Van Voorhees, MD      773-702-1323    bvanvoor@medicines.bsd.uchicago.edu

Illinois
      The University of Chicago, Chicago,  Illinois,  60637,  United States
Benjamin W. Van Voorhees, MD  773-702-3835    bvanvoor@medicine.bsd.uchicago.edu 
Benjamin W. Van Voorhees, MD,  Principal Investigator

Study chairs or principal investigators

Benjamin W Van Voorhees, MD,  Principal Investigator,  The University of Chicago, 5841 South Maryland Ave., MC 2007 Chicago, IL 60637   

More Information

Study ID Numbers:  C.A.T.C.H.-I.T. - 13240B; 13240B
Last Updated:  September 2, 2005
Record first received:  September 1, 2005
ClinicalTrials.gov Identifier:  NCT00145912
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-06

Resources



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Page Updated: February 22, 2005
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