Depression Management Project (DMP)
Primary Purpose
Major Depression, Depression
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-help cognitive-behavioral online course
Sponsored by
About this trial
This is an interventional treatment trial for Major Depression focused on measuring Cognitive Behavioral Therapy, Mood Management, Self-help, Internet
Eligibility Criteria
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
Sites / Locations
- University of California, San Francisco
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Self-help course
Arm Description
Outcomes
Primary Outcome Measures
Quick Inventory of Depressive Symptoms - Self-report
Secondary Outcome Measures
Full Information
NCT ID
NCT01150604
First Posted
June 23, 2010
Last Updated
November 13, 2018
Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH), Robert Wood Johnson Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01150604
Brief Title
Depression Management Project
Acronym
DMP
Official Title
Depression Management Project (DMP)
Study Type
Interventional
2. Study Status
Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH), Robert Wood Johnson Foundation
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression, Depression
Keywords
Cognitive Behavioral Therapy, Mood Management, Self-help, Internet
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
547 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Self-help course
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Self-help cognitive-behavioral online course
Intervention Description
A self-help online course based on cognitive behavioral therapy for major depression.
Primary Outcome Measure Information:
Title
Quick Inventory of Depressive Symptoms - Self-report
Time Frame
Baseline, 1, 2, and 5 months post consent
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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.
Exclusion Criteria:
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yan Leykin, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Depression Management Project
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