Viewing Study NCT00145951



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00145951
Status: TERMINATED
Last Update Posted: 2014-03-28
First Post: 2005-09-01

Brief Title: Reducing the Risk of Developing Major Depression in AdolescentsYoung Adults With Minor DepressionDepression Symptoms
Sponsor: University of Chicago
Organization: University of Chicago

Study Overview

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
Status: TERMINATED
Status Verified Date: 2014-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Lost funding
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this research study is to assess the feasibility of a combined primary careweb-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
Detailed Description: 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 careWeb-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 careWeb-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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None