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Sponsored by: |
University of Chicago |
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Information provided by: | University of Chicago |
ClinicalTrials.gov Identifier: | NCT00145951 |
The purpose of this research study is to assess the feasibility of a combined primary care/web-based depression prevention intervention. Primary care physicians (PCP) currently lack an alternative behaviorally-based approach to antidepressant medications for individuals with depression symptoms or minor depression, but who have not yet developed Major Depression.
The objective of this study is to compare the feasibility and efficacy of motivational interviewing (MI) versus brief advice in primary care to engage adolescents with a web-based depression prevention intervention.
Condition | Intervention |
---|---|
Depression |
Behavioral: motivational interviewing, brief advice in primary care |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Randomized Trial of a Motivational Interview Versus Brief Advice in Primary Care to Engage Mid-Late Adolescents With a Web-Based Depression Prevention Intervention |
Estimated Enrollment: | 125 |
Study Start Date: | May 2006 |
Estimated Study Completion Date: | September 2007 |
Groups/Cohorts | Assigned Interventions |
---|---|
1 | |
2 | |
3 |
Behavioral: motivational interviewing, brief advice in primary care
motivational interviewing, brief advice in primary care
|
There is no population-based approach to prevent the onset of major depression in adolescence. Adolescents with current sub-threshold depression symptoms (not meeting criteria for major depression, 5 < symptoms including depressed mood, irritability or loss of pleasure), a personal history of a depressive episode in the past or with a family history of depressive disorders are at increased risk. Because most adolescents have regular contact with primary care physicians, the primary care clinics could provide a setting to disseminate evidence-based preventive approaches. We have developed a combined primary care/Web-based preventive intervention to reduce the risk of developing depressive disorders in adolescents and young adults by adapting interventions of demonstrated benefit in study settings to a primary care/Web-based format in collaboration with leading investigators in the field. The goal of this research program is to evaluate the feasibility and possible efficacy of an alternative delivery mechanism for evidence-based behavioral approaches to depression treatment and prevention that have already demonstrated benefit with face-to-face delivery in study settings. Each component this intervention will need to be carefully evaluated for acceptability, safety, feasibility and efficacy. The focus of this study is the primary care component.
Ages Eligible for Study: | 14 Years to 75 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion criteria include:
Exclusion Criteria:
Contact: Benjamin Van Voorhees, MD | (773) 702-3835 | bvanvoor@medicine.bsd.uchicago.edu |
United States, Illinois | |
University of Chicago | Recruiting |
Chicago, Illinois, United States, 60637 | |
Contact: Benjamin Van Voorhees, MD 773-702-3835 bvanvoor@medicine.bsd.uchicago.edu | |
Principal Investigator: Benjamin Van Voorhees, MD |
Principal Investigator: | Benjamin Van Voorhees, MD | University of Chicago |
Responsible Party: | University of Chicago ( Dr. Benjamin VanVoorhees ) |
Study ID Numbers: | 13798A |
Study First Received: | September 1, 2005 |
Last Updated: | July 17, 2008 |
ClinicalTrials.gov Identifier: | NCT00145951 |
Health Authority: | United States: Institutional Review Board |
Depression Mental Disorders Mood Disorders |
Depressive Disorder, Major Depressive Disorder Behavioral Symptoms |