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NCT05518162 · ClinicalTrials.gov registry record · NA
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
A NA study, sponsored by University of Rochester.
- Completed
- Registry status
- NA
- Development phase
- 152
- Enrollment target
NCT05518162: Completed NA study, sponsored by University of Rochester.
NCT05518162 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 152 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05518162, a NA study, has completed, sponsored by University of Rochester.
- COMPLETED
- Registry status
- NA
- Development phase
- 152 participants
- Enrollment target
Study Summary
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).
Primary Outcome
The MINI is a binary assessment of the diagnosis of postpartum depression. It yields a yes, no answer.
Interventions
- BEHAVIORAL ROSE
- DEVICE InBloom
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 152 participants |
| Start Date | 2023-07-17 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
What the finished NCT05518162 record still lists
NCT05518162 is an interventional study that assigns participants to a tested intervention. The registered 152 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).
The record links to 0 conditions, and to 2 interventions - of which ROSE is the first listed.
NCT05518162 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05518162 about?
NCT05518162 is a clinical study titled "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". 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 Acce...
What is the current status of trial NCT05518162?
This trial is currently completed. It is a NA study. The enrollment target is 152 participants. The study started on 2023-07-17. Estimated completion is 2025-12-31.
What interventions are being tested in trial NCT05518162?
The interventions under investigation include: ROSE (BEHAVIORAL), InBloom (DEVICE).
Who is sponsoring clinical trial NCT05518162?
This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05518162's enrollment target sits among peer trials
152 658th of 2000 higher than 1,340 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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