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NCT05399784 · ClinicalTrials.gov registry record · NA
Postpartum Visit Timing and the Effect on Visit Attendance
A NA study of Postpartum Depression and Breastfeeding, sponsored by Women and Infants Hospital of Rhode Island.
- Completed
- Registry status
- NA
- Development phase
- 162
- Enrollment target
- 1
- Study location
NCT05399784 is a NA study of Postpartum Depression and Breastfeeding that has completed, run by Women and Infants Hospital of Rhode Island. The registered enrollment target is 162 participants, below the 530-participant average among 38 other Postpartum Depression trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05399784, a NA study of Postpartum Depression and Breastfeeding, has completed, sponsored by Women and Infants Hospital of Rhode Island.
- COMPLETED
- Registry status
- NA
- Development phase
- 162 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this study is to assess if the addition of an early postpartum visit improves attendance at postpartum visits. We seek to evaluate if an additional early postpartum visit improves patient education, satisfaction, or trust in the clinicians during the postpartum period; all of which may ultimately facilitate improved outcomes. Additionally, we seek to explore patient preferences for postpartum care delivery.
Conditions Studied
Interventions
- BEHAVIORAL Early postpartum visit
- BEHAVIORAL Standard postpartum visit
Study Locations (1)
Rhode Island
- Women & Infants Hospital - Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 162 participants |
| Start Date | 2021-02-01 |
| Est. Completion | 2023-06-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05399784
The ClinicalTrials.gov registry entry for NCT05399784 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 162 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 530-participant average among 38 other Postpartum Depression trials with a reported enrollment target (69% lower). The listed sponsor is Women and Infants Hospital of Rhode Island, which has 65 total studies on file at ClinicalTrials.gov.
The record links to 6 conditions, with Postpartum Depression appearing as the primary indexed condition, and to 2 interventions - of which Early postpartum visit is the first listed.
NCT05399784 reports 1 study location spanning 1 distinct geographic area - top geographies include Rhode Island.
Frequently Asked Questions
What is clinical trial NCT05399784 about?
NCT05399784 is a clinical study titled "Postpartum Visit Timing and the Effect on Visit Attendance". The objective of this study is to assess if the addition of an early postpartum visit improves attendance at postpartum visits. We seek to evaluate if an additional early postpartum visit improves patient education, satisfaction, or trust in the clinicians during the postpartum period; all of which ...
What is the current status of trial NCT05399784?
This trial is currently completed. It is a NA study. The enrollment target is 162 participants. The study started on 2021-02-01. Estimated completion is 2023-06-01.
What conditions does trial NCT05399784 study?
This clinical trial studies the following conditions: Postpartum Depression, Breastfeeding, Postpartum Weight Retention, Trust, Satisfaction, Patient.
What interventions are being tested in trial NCT05399784?
The interventions under investigation include: Early postpartum visit (BEHAVIORAL), Standard postpartum visit (BEHAVIORAL).
Who is sponsoring clinical trial NCT05399784?
This trial is sponsored by Women and Infants Hospital of Rhode Island, which has 65 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05399784 being conducted?
This trial has 1 study location across Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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