Responsive e-Health Intervention for Perinatal Depression in Healthcare Settings
Completed · Not applicable
Conditions studied: Perinatal Depression
In brief
Perinatal depression is experienced by at least 14-20% of pregnant and postpartum women, and is recognized as the most common complication of childbirth. In this project, the investigators plan to complete the process of making MomMoodBooster (MMB), a web-based cognitive-behavioral depression intervention, into a commercial ready product, MMB 2.0, that fits the workflow and staffing of healthcare organizations and is designed for both prenatal and postpartum women who are depressed. The investigators will also conduct a 2-arm randomized controlled trial to evaluate the efficacy of treatment as usual plus MMB 2.0 compared to treatment as usual in a large healthcare setting.
Key facts
- Study ID
- NCT03995316
- Run by
- Oregon Research Behavioral Intervention Strategies, Inc.
- People needed
- 191
- Starts
- 2018-08-24
- Expected to finish
- 2021-07-31
- Last updated by the study team
- 2023-10-12
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- pregnant or postpartum
- have elevated Edinburgh Postnatal Depression Scale (EPDS) of ≥ 12
- access to broadband internet and a computer at home (desktop, laptop, tablet) or a smartphone (iOS or Android)
- English language proficiency sufficient to enable completion of the informed consent and to engage in all study activities that are delivered in English
You may not qualify if…
- Women assessed with active suicidal ideation will be excluded and provided with immediate psychiatric care consistent with NorthShore's established safety protocol
Where it is running
- NorthShore University HealthSystem — Chicago, Illinois, United States
- Oregon Research Behavioral Intervention Strategies, Inc. — Springfield, Oregon, United States
Full record on ClinicalTrials.gov
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