Cognitive Behavioral Therapy Delivered Over the Internet for Women With Postpartum Depression
NCT ID: NCT00942721
Last Updated: 2013-11-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
53 participants
INTERVENTIONAL
2009-10-31
2013-04-30
Brief Summary
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Detailed Description
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Participation in this study will last 3 months. All participants will be offered a Web-based version of CBT for PPD. The CBT program will include guided behavioral strategies for dealing with depression, online videos of women who have used these strategies, Web forums in which participants can ask questions of peers and experts, and periodic phone coaching. The program will last 6 weeks. All participants will complete assessments at baseline, post-treatment, and 3-month follow-up. Safety monitoring questionnaires will also be completed at Weeks 2 and 4 of treatment. Assessments will include clinical interviews and questionnaires related to the following: health; depression; demographics; maternal skills, stress, and self-efficacy; Internet use, experience, and self-efficacy; behavioral self-efficacy; and program acceptability.
Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Web-based CBT for PPD
Participants will receive Web-based CBT for PPD.
Web-based CBT for PPD
A cognitive behavioral intervention that will provide participants with the following: online interactive tools to clarify their attitudes and reasons for wanting to change, information about some of the symptoms and mechanisms associated with feeling depressed during the postpartum period, and guidance on using behavioral and cognitive strategies proven to help reduce depressive symptoms
Interventions
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Web-based CBT for PPD
A cognitive behavioral intervention that will provide participants with the following: online interactive tools to clarify their attitudes and reasons for wanting to change, information about some of the symptoms and mechanisms associated with feeling depressed during the postpartum period, and guidance on using behavioral and cognitive strategies proven to help reduce depressive symptoms
Eligibility Criteria
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Inclusion Criteria
* Home access to the Internet
* Use of personal e-mail
* Score from 12 to 20, inclusive, on the Edinburgh Postnatal Depression Scale
* Diagnosed as having postpartum depression
Exclusion Criteria
* Currently receiving treatment for depressive symptoms, including antidepressant medication or psychotherapy
* Currently has suicidal intentionality, lethality, access to means, and history of suicide attempts
18 Years
FEMALE
No
Sponsors
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National Institute of Mental Health (NIMH)
NIH
Oregon Research Institute
OTHER
Responsible Party
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Principal Investigators
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Brian G. Danaher, PhD
Role: PRINCIPAL_INVESTIGATOR
Oregon Research Institute
Jeannette Milgrom, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Melbourne
Scott Stuart, MD
Role: PRINCIPAL_INVESTIGATOR
University of Iowa
Locations
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University of Iowa
Iowa City, Iowa, United States
Oregon Research Institute
Eugene, Oregon, United States
University of Melbourne
Heidelberg Heights, Victoria, Australia
Countries
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References
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Danaher BG, Milgrom J, Seeley JR, Stuart S, Schembri C, Tyler MS, Ericksen J, Lester W, Gemmill AW, Lewinsohn P. Web-Based Intervention for Postpartum Depression: Formative Research and Design of the MomMoodBooster Program. JMIR Res Protoc. 2012 Nov 22;1(2):e18. doi: 10.2196/resprot.2329.
Danaher BG, Milgrom J, Seeley JR, Stuart S, Schembri C, Tyler MS, Ericksen J, Lester W, Gemmill AW, Kosty DB, Lewinsohn P. MomMoodBooster web-based intervention for postpartum depression: feasibility trial results. J Med Internet Res. 2013 Nov 4;15(11):e242. doi: 10.2196/jmir.2876.
Other Identifiers
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