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Sponsors and Collaborators: |
University of Chicago Centers for Disease Control and Prevention |
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Information provided by: | University of Chicago |
ClinicalTrials.gov Identifier: | NCT00152529 |
The purpose of this study is to adapt depression prevention interventions of proven benefit to the primary care setting in a manner that would be acceptable and potentially available to young adults in the community.
Condition | Intervention |
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Depression |
Behavioral: Screening (Behavior) |
Study Type: | Observational |
Study Design: | Screening, Longitudinal, Defined Population, Retrospective/Prospective Study |
Official Title: | “C.A.T.C.H.-I.T.” Competent Adulthood Transition With Cognitive, Humanistic and Interpersonal Teaching |
Estimated Enrollment: | 8 |
Study Start Date: | October 2003 |
Estimated Study Completion Date: | June 2004 |
Our study goal is to develop a prototype combination primary care-web based depression intervention for young adults ages 18-24years in urban community and university settings. The content development will include: (1) two brief (15 minutes) primary care counseling sessions, (2) one introductory web based module, (3) four web-based cognitive behavior teaching modules, (4) three web-based modules discussing relationship building skills (IPT), and (5) a final web module discussing self-recognition, evidence-based treatment, and stigma. Eight young adult volunteers will evaluate the program in three loops of evaluation and revision in a modified focus group approach. This protocol was approved by the Johns Hopkins Joint Committee on Clinical Investigations.
Primary Outcomes:
The primary outcome variables relate to the functionality and acceptability of the intervention. These variables include readability, ease of understanding, acceptability, and helpfulness of each component of the intervention, and a global rating of each
Secondary Outcomes:
Process measures (time on site, exercise completion), outcomes (mood and intermediate outcomes-social adjustment, dysfunctional thinking), and knowledge and opinions of current treatments for depression. These data will be helpful in planning for a future Focus groups of 5-10 individuals have been used successfully to provide initial product evaluations or to develop general themes in attitude research. Summary statistics will be collected.
Ages Eligible for Study: | 18 Years to 25 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
United States, Illinois | |
The University of Chicago | |
Chicago, Illinois, United States, 60637 |
Principal Investigator: | Benjamin W Van Voorhees, MD | The University of Chicago, 5841 South Maryland Ave., MC 2007 Chicago, IL 60637 |
Study ID Numbers: | 12591A, U48/CCU309674 - 12591A |
Study First Received: | September 7, 2005 |
Last Updated: | April 30, 2007 |
ClinicalTrials.gov Identifier: | NCT00152529 |
Health Authority: | United States: Institutional Review Board |
Depression, educational site for depression |
Depression Mental Disorders Mood Disorders Depressive Disorder Behavioral Symptoms |