Organized Self-Management Support Services for Chronic Depression (Stride)

This study is enrolling participants by invitation only.

Sponsor:

Collaborator:

Swedish Medical Center

Information provided by:

Group Health Cooperative

ClinicalTrials.gov Identifier:

NCT01139060

First received: June 4, 2010

Last updated: June 7, 2010

Last verified: June 2010

History of Changes

Tracking Information
First Received Date ^ICMJE	June 4, 2010
Last Updated Date	June 7, 2010
Start Date ^ICMJE	August 2009
Primary Completion Date	Not Provided
Current Primary Outcome Measures ^ICMJE (submitted: June 7, 2010)	Evaluate the program's effectiveness
Original Primary Outcome Measures ^ICMJE	Same as current
Change History	Complete list of historical versions of study NCT01139060 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE (submitted: June 7, 2010)	Examination of moderators of treatment response An estimate of the program's costs and effect on the costs of treatment for depression
Original Secondary Outcome Measures ^ICMJE	Same as current
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Organized Self-Management Support Services for Chronic Depression
Official Title ^ICMJE	Organized Self-Management Support Services for Chronic Depression
Brief Summary	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	Not Provided
Study Type ^ICMJE	Interventional
Study Phase	Not Provided
Study Design ^ICMJE	Not Provided
Condition ^ICMJE	Depression
Intervention ^ICMJE	Behavioral: organized care program for chronic or recurrent depression
Study Arm (s)	Experimental: Intervention Group Intervention: Behavioral: organized care program for chronic or recurrent depression No Intervention: Usual Care
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Enrolling by invitation
Enrollment ^ICMJE	Not Provided
Completion Date	Not Provided
Primary Completion Date	Not Provided
Eligibility Criteria ^ICMJE	Inclusion Criteria: all patients will meet criteria for recurrent major depression or dysthymia Exclusion Criteria: bipolar disorder or psychotic disorder
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	Not Provided
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	United States

Administrative Information
NCT Number ^ICMJE	NCT01139060
Other Study ID Numbers ^ICMJE	5R01MH082995
Has Data Monitoring Committee	Yes
Responsible Party	Evette Ludman, PhD, Research Associate, Group Health Research Institute
Study Sponsor ^ICMJE	Group Health Cooperative
Collaborators ^ICMJE	Swedish Medical Center
Investigators ^ICMJE	Not Provided
Information Provided By	Group Health Cooperative
Verification Date	June 2010
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top