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

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Oregon Research Institute

Status and phase

Completed
Phase 3
Phase 2

Conditions

Depression

Treatments

Behavioral: Cognitive-behavioral bibliotherapy
Behavioral: Cognitive-behavioral group

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00904891
R01MH080853 (U.S. NIH Grant/Contract)
DSIR 84-CTP

Details and patient eligibility

About

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

Full description

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.

Enrollment

390 patients

Sex

All

Ages

13 to 19 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • High school student
  • Subthreshold depressive symptoms

Exclusion criteria

  • Meets criteria for major depression or dysthymia

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

390 participants in 3 patient groups

1
Experimental group
Description:
Participants will receive a cognitive-behavioral group intervention.
Treatment:
Behavioral: Cognitive-behavioral group
2
Active Comparator group
Description:
Participants will receive cognitive-behavioral bibliotherapy.
Treatment:
Behavioral: Cognitive-behavioral bibliotherapy
3
No Intervention group
Description:
Participants will only complete study assessments.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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