Depression Management Project

Depression Clinical Trial

— DMP  

Official title:

Depression Management Project (DMP)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01150604
• Other study ID #: T32MH019391
• Status: Completed
• Phase: N/A
• Start date: June 2010
• Est. completion date: June 2013

Study information

• Verified date: November 2018
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 547
• Est. completion date: June 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• Depressive Disorder, Major
• Major Depression

Intervention

Behavioral:
• Self-help cognitive-behavioral online course
A self-help online course based on cognitive behavioral therapy for major depression.

Locations

Country	Name	City	State
United States	University of California, San Francisco	San Francisco	California

Sponsors (3)

Lead Sponsor	Collaborator
University of California, San Francisco	National Institute of Mental Health (NIMH), Robert Wood Johnson Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quick Inventory of Depressive Symptoms - Self-report		Baseline, 1, 2, and 5 months post consent