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Postnatal Debriefing After Adverse Obstetric Events

Study acronym: DBIRTH
StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Interventions: Structured Postnatal Debriefing (Behavioral) to Structured Postnatal Debriefing (Behavioral), Usual Care (Other)
    • Secondary endpoints: details revised at 1 of 4 entries
    • Study description expanded, about 41 words
    v3
  2. Minor Secondary endpoints: details revised at 3 of 4 entries
    • Study title shortened, about 4 words
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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Adverse or unexpected obstetric events can negatively affect women's psychological well-being and childbirth experience, increasing the risk of postpartum traumatic stress. However, structured postnatal debriefing is not routinely implemented in clinical practice, and evidence regarding its effectiveness remains limited. This study aims to evaluate the effect of a structured postnatal debriefing conducted within the first 24 hours after childbirth in women who have experienced an adverse or unexpected obstetric event. This quasi-experimental pretest-posttest study will include two consecutive groups: a control group receiving usual postpartum care during the pre-implementation phase and an intervention group receiving structured postnatal debriefing during the implementation phase. The primary outcome is childbirth-related trauma at 6 weeks postpartum. Secondary outcomes include birth satisfaction, early post-traumatic stress symptoms, satisfaction with information and emotional support received after childbirth, and clinical maternal and neonatal outcomes. This study will provide evidence on whether structured postnatal debriefing improves psychological outcomes and contributes to more patient-centered obstetric care.
Trial Details
NCT Number NCT07579273
Lead Sponsor Parc de Salut Mar
Conditions
(from sponsor)
Stress Disorders, Post-Traumatic, Psychological Trauma, Obstetric Labor Complications, Postpartum Period
Related terms Birth Injuries, Obstetric Labor Complications, Psychological Trauma, Stress Disorders, Post-Traumatic
Enrollment 142 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov