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NCT07071025 · ClinicalTrials.gov registry record · NA
Preventing Perinatal Anxiety: Testing an Internet-delivered Intervention
A NA study, sponsored by West Virginia University.
- Not yet
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT07071025: Clinical Trial NA study, sponsored by West Virginia University.
NCT07071025 is a NA study that has not yet begun recruiting, run by West Virginia University. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07071025, a NA study, has not yet begun recruiting, sponsored by West Virginia University.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
Postpartum anxiety disorders are the most prevalent postpartum psychiatric conditions. The purpose of this study is to evaluate the Internet-delivered postpartum anxiety and obsessive-compulsive disorder (OCD) prevention program, called "Preventing Postpartum Onset Distress", or P-POD. The overarching goal of this study is to conduct a randomized control trial of P-POD, an online program designed to reduce and prevent perinatal anxiety in at-risk women in West Virginia. Investigators will test the effects of P-POD compared to an anxiety education control intervention on risk factors for perinatal anxiety and assess mothers' anxiety symptoms, relationships with their partners, and relationships with their infants at 8-weeks postpartum. Eligible women and their partners will be consented at the start of the second trimester of pregnancy. Couples will be randomized into either the P-POD (active) or ANX-ED (control) intervention. Couples will then begin to work through the ten intervention modules: seven modules for women, at a recommended rate of one per week, and three modules for partners, at a recommended rate of no more than one per week. Women will complete brief weekly phone "coaching calls" to encourage module completion, ensure understanding of material, and answer any content-related or technical questions. Ten weeks after the pre-intervention assessment, women will complete the post-intervention assessment (same measures as pre-assessment).
Primary Outcome
Change in STAI-Trait score. This is a 20-item self-report used to assess dispositional levels of anxiety. It is widely used, sensitive to treatment, has strong psychometric properties, and includes items that would be relevant to pregnant women. The STAI-Trait Total Score will be used before and after P-POD to assess change in prenatal trait anxiety. The STAI-Trait total score ranges from 20 to 80. Higher numbers represent more anxiety (worse outcome).
Interventions
- BEHAVIORAL Preventing Postpartum Onset Distress (P-POD)
- BEHAVIORAL Anxiety Education (ANX-ED)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-08 |
| Est. Completion | 2027-12 |
| Phase | NA |
What is known before NCT07071025 opens enrollment
NCT07071025 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (93% lower).
The record links to 0 conditions, and to 2 interventions - of which Preventing Postpartum Onset Distress (P-POD) is the first listed.
NCT07071025 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07071025 about?
NCT07071025 is a clinical study titled "Preventing Perinatal Anxiety: Testing an Internet-delivered Intervention". Postpartum anxiety disorders are the most prevalent postpartum psychiatric conditions. The purpose of this study is to evaluate the Internet-delivered postpartum anxiety and obsessive-compulsive disorder (OCD) prevention program, called "Preventing Postpartum Onset Distress", or P-POD. The overarchi...
What is the current status of trial NCT07071025?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-08. Estimated completion is 2027-12.
What interventions are being tested in trial NCT07071025?
The interventions under investigation include: Preventing Postpartum Onset Distress (P-POD) (BEHAVIORAL), Anxiety Education (ANX-ED) (BEHAVIORAL).
Who is sponsoring clinical trial NCT07071025?
This trial is sponsored by West Virginia University, which has 122 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07071025's enrollment target sits among peer trials
100 840th of 2000 higher than 1,081 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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