Depression Clinical Trial
Official title:
Using the Internet for English/Spanish Randomized Trials for Postpartum Depression
Verified date | April 2014 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The original trial will evaluate the effectiveness of a Web-based program in preventing postpartum depression. The site has been modified to provide materials from both conditions.
Status | Completed |
Enrollment | 1000 |
Est. completion date | June 2013 |
Est. primary completion date | June 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Pregnant - Fluent in English or Spanish |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | University of California, San Francisco | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | National Institute of Mental Health (NIMH) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Edinburgh Postnatal Depression Scale (EPDS) | Measured monthly for 6 months postpartum | Yes | |
Secondary | Center for Epidemiologic Studies-Depression (CES-D) Scale | Measured monthly for 6 months postpartum | Yes |
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