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NCT03563339 · ClinicalTrials.gov registry record · NA
Internet-delivered Postpartum Anxiety Prevention
A NA study, sponsored by West Virginia University.
- Completed
- Registry status
- NA
- Development phase
- 19
- Enrollment target
NCT03563339 is a NA study that has completed, run by West Virginia University. The registered enrollment target is 19 participants.
The verdict
NCT03563339, a NA study, has completed, sponsored by West Virginia University.
- COMPLETED
- Registry status
- NA
- Development phase
- 19 participants
- Enrollment target
Study Summary
Postpartum anxiety disorders are the most prevalent postpartum psychiatric conditions. Up to 16% of mothers experience postpartum anxiety or related disorders, such as OCD. With respect to the investigator's own community, this means that up to 3,313 women in West Virginia may struggle with postpartum anxiety or OCD. Left untreated, perinatal anxiety and OCD are associated with numerous adverse outcomes, such as maternal depression, preterm birth, impaired fetal development, low birthweight, difficulty breastfeeding, anxiety in children, and interference with parent-infant bonding. Critically, anxiety is a risk factor for cardiovascular disease and substance use disorders, both significant West Virginia health disparities. Thus, there is a critical need to develop effective and scalable prevention programs to address postpartum anxiety and OCD. The purpose of this proposed community-engaged study is to develop and test the feasibility, usability, and acceptability of an Internet-delivered postpartum anxiety and OCD prevention program, called "Preventing Postpartum Onset Distress", or P-POD.
Interventions
- BEHAVIORAL P-POD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2020-04-08 |
| Est. Completion | 2021-12-13 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03563339
The ClinicalTrials.gov registry entry for NCT03563339 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 19 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is West Virginia University, which has 122 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which P-POD is the first listed.
NCT03563339 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03563339 about?
NCT03563339 is a clinical study titled "Internet-delivered Postpartum Anxiety Prevention". Postpartum anxiety disorders are the most prevalent postpartum psychiatric conditions. Up to 16% of mothers experience postpartum anxiety or related disorders, such as OCD. With respect to the investigator's own community, this means that up to 3,313 women in West Virginia may struggle with postpart...
What is the current status of trial NCT03563339?
This trial is currently completed. It is a NA study. The enrollment target is 19 participants. The study started on 2020-04-08. Estimated completion is 2021-12-13.
What interventions are being tested in trial NCT03563339?
The interventions under investigation include: P-POD (BEHAVIORAL).
Who is sponsoring clinical trial NCT03563339?
This trial is sponsored by West Virginia University, which has 122 total clinical trials registered on ClinicalTrials.gov.
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