Online Collaborative Learning Intervention to Prevent Perinatal Depression
Completed · Not applicable
Conditions studied: Depression, Postpartum
In brief
The overarching aim of this project is to develop and pilot an innovative online intervention (Share) that integrates an Individual Internet Intervention (III) and an Internet Support Group (ISG) in preventing Postpartum Major Depression (PPMD). To establish that supportive accountability is a critical component of the intervention, Share will be compared to an III alone, and an ISG without the III components.
Key facts
- Study ID
- NCT02121015
- Run by
- University of Illinois at Chicago
- People needed
- 210
- Starts
- 2016-05-01
- Expected to finish
- 2017-11-01
- Last updated by the study team
- 2020-01-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women who are:
- 18 years and older
- Pregnant and between 20 and 28 weeks gestation and for whom there is an expectation of a full 40 week gestation at the birth of their child
- Have a Patient Health Questionnaire (PHQ-9) score score between 5-14
- Have access to a broadband internet connection
- Are able to read and speak English
You may not qualify if…
- Women who:
- Have visual, hearing, voice, or motor impairment that would prevent completion of study procedures
- Are diagnosed with a psychotic disorder, bipolar disorder, dissociative disorder, substance use disorder or other diagnosis using the Mini International Neuropsychiatric Interview (MINI) for which participation in this trial is either inappropriate or dangerous
- Are currently receiving treatment (medication or psychotherapy), or have an intention to resume antidepressant medication after delivery (i.e., women who discontinued their medication during pregnancy)
- Are suicidal (i.e., have ideation, plan, and intent)
Where it is running
- University of Illinois at Chicago — Chicago, Illinois, United States
- Northwestern University — Chicago, Illinois, United States
- University of Iowa — Iowa City, Iowa, United States
Full record on ClinicalTrials.gov
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