Depression Management Project
DMP
1 other identifier
interventional
547
1 country
1
Brief Summary
The purpose of this study is to determine whether an eight-lesson self-help intervention delivered online will result in a reduction of depressive symptoms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2010
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2010
CompletedFirst Submitted
Initial submission to the registry
June 23, 2010
CompletedFirst Posted
Study publicly available on registry
June 25, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedNovember 15, 2018
November 1, 2018
3 years
June 23, 2010
November 13, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Quick Inventory of Depressive Symptoms - Self-report
Baseline, 1, 2, and 5 months post consent
Study Arms (1)
Self-help course
EXPERIMENTALInterventions
A self-help online course based on cognitive behavioral therapy for major depression.
Eligibility Criteria
You may qualify if:
- Participants will be 18 years of age or older,
- Participants will have regular (\>1 time/week) access to internet and email, with a valid email address,
- Participants will be fluent or almost fluent in English, and
- Participants will be looking for information to help themselves, rather than another person.
- Only those invited to participate will be eligible.
You may not qualify if:
- Participants under 18 years of age,
- Participants will with sporadic (\< 1 time/week) access to internet and email,
- Participants who fail to provide an email address,
- Participants with English difficulties,
- Participants looking for information to help someone else, and
- Participants not invited will be ineligible.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of California, San Franciscolead
- National Institute of Mental Health (NIMH)collaborator
- Robert Wood Johnson Foundationcollaborator
Study Sites (1)
University of California, San Francisco
San Francisco, California, 94143, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yan Leykin, PhD
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 23, 2010
First Posted
June 25, 2010
Study Start
June 1, 2010
Primary Completion
June 1, 2013
Study Completion
June 1, 2013
Last Updated
November 15, 2018
Record last verified: 2018-11