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Treatment of Post-partum Depression Using an Behavioral Intervention Called ROSE (Reach Out, Stay Strong, Essentials for Mothers of Newborns) Delivered Using an Electronic App

Recruiting
18 years of age
Female
Phase N/A

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Overview

A randomized trial of pregnant people at risk for postpartum depression comparing the InBloom app (n = 76) to ROSE (n = 76; weekly scheduled group), and two control groups. We will assess Depression at baseline and 1, 2 and 3 months, ROI at 3 months, Satisfaction at 1 and 3 months and Perceived Access at 1 and 3 months. Subject participation will last up to 8 months (minimum 17 weeks pregnant through 3 months postpartum).

Eligibility

Inclusion Criteria:

  • 17-32 weeks pregnant
  • enrolled for prenatal care in one of the five identified practices
  • English speaking
  • able to use an app (audio/visual/dexterity)
  • have one or more of the following PPD risk factors: Medicaid eligible; anxiety (GAD-7 > 10) during pregnancy; mild to moderate depressive symptoms (PHQ-9 = 10-19); self-reported history of depression treatment; gestational diabetes; and/or young age (18-21 years).

Exclusion Criteria:

  • patients with acute mental health needs
  • cannot communicate in English
  • demonstrate significant cognitive impairment
  • are planning to place the child for adoption
  • PHQ-9 depression score > 19
  • younger than age 18

Study details

Post-partum Depression

NCT05518162

University of Rochester

25 January 2024

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