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Clinical Trials/NCT00145054
NCT00145054
Completed
Phase 2

Randomized, Controlled Pilot Study of a Self-Help Depression Skills Program for College-Aged Youth

Kaiser Permanente1 site in 1 country150 target enrollmentSeptember 5, 2005
ConditionsDepression

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Depression
Sponsor
Kaiser Permanente
Enrollment
150
Locations
1
Primary Endpoint
self-reported depression on the CES-D
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

We propose to conduct a pilot trial of an Internet-only depression skills training program for adolescents and young adults. The intervention, MoodHelper.org already exists and has been tested in two pilots. In this third pilot, we plan to use an enriched minority sampling frame to mail 3,000 to 6,000 invitational brochures to KPNW members aged 14 to 24, with a enrollment target of 150. Interested members will go to the study Internet site, and if they choose to participate, complete the online consent and assessment battery (used in the previous pilots). Participants will be randomly assigned by the site's software to one of two conditions: (1) the "Intervention" condition, with complete access to the SADhelper.org web site or (2) the "Usual Care" condition, with access to all Internet sites and KPNW health care, but with no access to the therapeutic portion of the SADhelper site. All participants (those with and without access to the research intervention) will be reminded by e-mail and, if necessary, by telephone to return to the web site and complete follow-up questionnaires four, eight, sixteen, and thirty-two weeks after enrolling in the study.

Detailed Description

We propose to conduct a pilot trial of an Internet-only depression skills training program for adolescents and young adults. The intervention, MoodHelper.org already exists and has been tested in two pilots. In this third pilot, we plan to use an enriched minority sampling frame to mail 3,000 to 6,000 invitational brochures to KPNW members aged 14 to 24, with a enrollment target of 150. Interested members will go to the study Internet site, and if they choose to participate, complete the online consent and assessment battery (used in the previous pilots). Participants will be randomly assigned by the site's software to one of two conditions: (1) the "Intervention" condition, with complete access to the SADhelper.org web site or (2) the "Usual Care" condition, with access to all Internet sites and KPNW health care, but with no access to the therapeutic portion of the SADhelper site. All participants (those with and without access to the research intervention) will be reminded by e-mail and, if necessary, by telephone to return to the web site and complete follow-up questionnaires four, eight, sixteen, and thirty-two weeks after enrolling in the study.

Registry
clinicaltrials.gov
Start Date
September 5, 2005
End Date
TBD
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • current clinical diagnosis of depression Internet access

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

self-reported depression on the CES-D

Secondary Outcomes

  • health care utilization

Study Sites (1)

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