Online Intervention to Prevent Perinatal Depression and Promote Breastfeeding

Completed · Not applicable

Conditions studied: Depression, Breastfeeding

In brief

"SunnysidePlus" will functionally integrate a web based intervention targeting skills to promote and support breastfeeding, manage mood,and prevent depression. Sunnyside Plus will build upon the previously tested "Sunnyside" intervention which targeted skills to manage mood through an interactive website with didactic material and tools. Women in weeks 20-28 of their pregnancy will be randomized to receive either Sunnyside Plus or Sunnyside. The Sunnyside intervention will consist of 6 weeks of online lessons during pregnancy and booster sessions at 2 weeks, 4 weeks, and 6 weeks postpartum. Sunnyside Plus will include additional education and support to improve breastfeeding outcomes. Breastfeeding education and skills will be provided during the 6 weeks of online lessons during pregnancy. Breastfeeding support will continue through 6 weeks postpartum. This postpartum support will involve weekly online lessons, text support, and video support calls with a Lactation Educator provided on an as-needed basis. SunnysidePlus has the potential to provide a novel paradigm for improving breastfeeding outcomes and preventing depression; one that is accessible, highly scalable and cost-effective.

Key facts

Study ID

NCT04128202

Run by

University of Illinois at Chicago

People needed

22

Starts

2020-06-15

Expected to finish

2021-07-15

Last updated by the study team

2021-07-26

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female
• Black or African American
• 18 years and older
• Pregnant and between 20 and 28 weeks gestation
• Intend to breastfeed their child
• Have a score of 5-14 on the Patient Health Questionnaire-8 (PHQ-8)
• Have access to a broadband internet connection
• Are able to read and speak English

You may not qualify if…

• Are pregnant with multiples
• Have visual, hearing, voice, or motor impairment that would prevent completion of study procedures
• Diagnosed with a major depressive episode, psychotic disorder, bipolar disorder, dissociative disorder, substance use disorder or other diagnosis for which participation in this trial is either inappropriate or dangerous based on self-report
• Are currently receiving treatment (medication or psychotherapy),have an intention to resume antidepressant medication after delivery (i.e., women who discontinued their medication during pregnancy).

Where it is running

• University of Illinois at Chicago — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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