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Completed

NCT Number: NCT00904891

Testing the Effectiveness of Adolescent Depression Prevention Programs (The OregonBlues Study)

This study will test the effectiveness of two programs for preventing depression in adolescents.

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Key information

Age range

13 year–19 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Oregon Research Institute

Eugene, Oregon, 97403, United States

About this study

Major depression is one of the most common psychiatric disorders experienced by adolescents. Even adolescents with depressive symptoms below the level of diagnosis are at increased risk of a range of future problems, such as psychiatric disorders, impaired social functioning, and substance abuse.

Depression prevention therapies have had mixed results. Those that are implemented universally have shown little efficacy, although those that specifically target adolescents at risk of depression have shown greater efficacy. A large scale effectiveness trial-one that applies treatments outside of a lab in "real world" settings-of a targeted depression prevention therapy has not been conducted. This study will test the effectiveness of two therapies for preventing depression in adolescents. The first is a brief, group cognitive-behavioral depression prevention program, and the second is bibliotherapy, which involves giving participants a self-help book for depression. Bibliotherapy has shown efficacy in previous research but has not been examined in an effectiveness trial.

Participation in this study will last 24 months. Participants will be randomly assigned to one of three conditions: a six-session, cognitive-behavioral depression prevention group; a bibliotherapy group; and an assessment only group. Participants in the cognitive-behavioral group will meet with a study therapist and other group members to learn strategies for preventing depression. Participants in the bibliotherapy group will be given a self-help book titled "Feeling Good" with information on preventing depression. Participants in the assessment only group will receive a pamphlet on depression symptoms and treatment. All participants will complete assessments at baseline; after the cognitive-behavioral group has been completed; and at 6-, 12-, 18-, and 24-month follow-ups. These assessments will include an interview about depression symptoms and a survey about thoughts, feelings, actions, depression, and substance abuse.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • High school student
  • Subthreshold depressive symptoms

Exclusion criteria

  • Meets criteria for major depression or dysthymia

Treatment and study plan

Cognitive-behavioral group

Behavioral

Six sessions of cognitive-behavioral depression prevention group intervention

Cognitive-behavioral bibliotherapy

Behavioral

Cognitive-behavioral bibliotherapy, delivered from the book "Feeling Good"

Primary outcomes

  1. Depressive symptoms obtained from Kiddie-Schedule for Affective Disorders and Schizophrenia (K-SADS)

    Time frame: Measured at baseline; post-treatment; and after 6, 12, 18, and 24 months

Secondary outcomes

  1. Score on Beck Depression Inventory (BDI)

    Time frame: Measured at baseline; post-treatment; and after 6, 12, 18, and 24 months

Sponsors and collaborators

Lead sponsor

Oregon Research Institute

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Effectiveness Trial of an Adolescent Depression Prevention Program

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
May 20, 2009
Registry last updated
Mar 12, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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