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Organized Self-Management Support Services for Chronic Depression

NCT ID: NCT01139060

Last Updated: 2017-10-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

302 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-08-31

Brief Summary

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The purpose is to test the effectiveness of an organized care program for chronic or recurrent depression. Using a two-arm design, the investigators will randomly assign 300 participants with chronic or recurrent depression to one of two conditions: continued usual care (UC); or an 18-month organized treatment program focused on outreach and engagement, including a weekly group self-management training program, monthly visits with a psychotherapist (in-person or by telephone), and optional one-on-one visits with a peer support specialist. All intervention components are intended as adjuncts to any existing depression treatment (usually antidepressant medication) provided by participants' regular providers.

Detailed Description

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Conditions

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Depression

Keywords

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chronic or recurrent depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Intervention Group

18-month organized treatment program focused on outreach and engagement for chronic or recurrent depression

Group Type EXPERIMENTAL

organized care program for chronic or recurrent depression

Intervention Type BEHAVIORAL

Usual Care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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organized care program for chronic or recurrent depression

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* all patients will meet criteria for recurrent major depression or dysthymia

Exclusion Criteria

* bipolar disorder or psychotic disorder
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Swedish Medical Center

OTHER

Sponsor Role collaborator

Kaiser Permanente

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Evette Ludman, PhD

Role: PRINCIPAL_INVESTIGATOR

Group Health Research Institute

Locations

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Group Health Research Insitute

Seattle, Washington, United States

Site Status

Swedish Cherry Hill Clinic

Seattle, Washington, United States

Site Status

Countries

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United States

References

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Jones SMW, Ludman EJ. Factor Structure and Sensitivity to Change of the Recovery Assessment Scale. J Behav Health Serv Res. 2018 Oct;45(4):690-699. doi: 10.1007/s11414-017-9563-x.

Reference Type DERIVED
PMID: 28726086 (View on PubMed)

Ludman EJ, Simon GE, Grothaus LC, Richards JE, Whiteside U, Stewart C. Organized Self-Management Support Services for Chronic Depressive Symptoms: A Randomized Controlled Trial. Psychiatr Serv. 2016 Jan;67(1):29-36. doi: 10.1176/appi.ps.201400295. Epub 2015 Aug 17.

Reference Type DERIVED
PMID: 26278222 (View on PubMed)

Other Identifiers

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5R01MH082995

Identifier Type: NIH

Identifier Source: org_study_id

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