Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06992791 · ClinicalTrials.gov registry record · NA

Labor Education to Reduce Postpartum Traumatic Stress

A NA study, sponsored by University of California, San Diego.

Active
Registry status
NA
Development phase
400
Enrollment target

NCT06992791: Active NA study, sponsored by University of California, San Diego.

NCT06992791 is a NA study that is active but no longer recruiting, run by University of California, San Diego. The registered enrollment target is 400 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06992791, a NA study, is active but no longer recruiting, sponsored by University of California, San Diego.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
400 participants
Enrollment target

Study Summary

The goal of this randomized controlled trial is determine if education on common events in labor in nulliparous women can reduce the postpartum traumatic symptoms. The main question it aims to answer are: * Does prenatal education on labor events reduce post-traumatic symptoms, as measured by thePost Traumatic Stress Disorder Cecklist for Diagnostic and Statistical Manual for Mental Health Disorders (PCL-5) at 6 weeks postpartum? * Does prenatal education on labor affect labor outcomes? Participants will be given surveys: * At enrollment on mental health and previous traumatic experiences * After education on expectations on childbirth * After delivery on experience of childbirth * At 6 weeks and 6 months postpartum on traumatic symptoms and mental health outcomes. They will also have the option to participate in collection of discarded cerebrospinal fluid, blood and serum and physiologic sensitivity testing.

Primary Outcome

Validated measurement for PTSD, scores 0-80 with higher being more symptomatic

Interventions

  • BEHAVIORAL Prenatal Education on Childbirth

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2025-10-14
Est. Completion 2027-06-30
Phase NA
University of California, San Diego

775 total trials

What the registry record for NCT06992791 still lists

NCT06992791 is an interventional study that assigns participants to a tested intervention. The registered 400 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 (72% lower).

The record links to 0 conditions, and to 1 intervention - of which Prenatal Education on Childbirth is the first listed.

NCT06992791 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06992791 about?

NCT06992791 is a clinical study titled "Labor Education to Reduce Postpartum Traumatic Stress". The goal of this randomized controlled trial is determine if education on common events in labor in nulliparous women can reduce the postpartum traumatic symptoms. The main question it aims to answer are: * Does prenatal education on labor events reduce post-traumatic symptoms, as measured by thePo...

What is the current status of trial NCT06992791?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 400 participants. The study started on 2025-10-14. Estimated completion is 2027-06-30.

What interventions are being tested in trial NCT06992791?

The interventions under investigation include: Prenatal Education on Childbirth (BEHAVIORAL).

Who is sponsoring clinical trial NCT06992791?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06992791's enrollment target sits among peer trials

400 246th of 2000 higher than 1,734 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01665326 · 400 participants

    Determination of CRIM Status and Longitudinal Follow-up of Individuals With Pompe Disease

  • NCT02108054 · 400 participants · NA

    Behavioral and Functional Task Development, Implementation, and Testing

  • NCT02216500 · 400 participants · NA

    Ketogenic Therapy Effects on Electrical and Metabolic Abnormalities in Epilepsy

  • NCT02250352 · 400 participants

    Core Biopsies for Establishing a Breast Tumor Tissue Repository

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06992791, the US trial registry maintained by the National Library of Medicine. NCT06992791 (mid enrollment · none site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.