Improving postpartum quality of life with enhanced perineal care training for first-time mothers after term vaginal birth
Official title: Effect of Structured Perineal Care Training on Postpartum Quality of Life and Sonographic Maternal Injury Detection
Run by University Hospital Hradec Kralove · NCT07865065 · Data updated 2026-11-12
This intervention study tests whether structured obstetric training for perineal protection, episiotomy technique, and early detection and repair of obstetric anal sphincter injuries can improve early postpartum quality of life for first-time mothers after a term vaginal birth.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 380 (estimated) |
| Sponsor | University Hospital Hradec Kralove Academic / other |
| Locations | 1 site (Hradec Králové) |
| Status | Recruiting |
| Started | July 1, 2025 |
| Main results expected | November 2026 |
| Study ends | January 2027 |
| Registry record updated | October 8, 2026 |
| Trial ID | NCT07865065 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Primiparous women delivering vaginally at term (≥ 36 weeks) who are 18 years or older, with singleton pregnancies and no prior anorectal disease or incontinence.
✕Probably not a fit
Women with prior obstetric history, multiparity, preexisting anorectal conditions, or non-vaginal deliveries may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective before-and-after study enrolls primiparous women who have a term vaginal delivery to see if a structured obstetric training program reduces postpartum pelvic floor trauma and improves quality of life. The program includes perineal protection, better episiotomy technique, systematic OASI detection, and hands-on repair. Primary outcomes focus on postpartum anal incontinence and stress urinary incontinence; secondary outcomes include ultrasound markers of pelvic floor integrity. The study uses a baseline cohort and compares outcomes after implementing the training. Participants are adults 18 or older with singleton pregnancies and no prior anorectal disease.
Why it matters
Potential benefit: If successful, the training could reduce postpartum pelvic floor injuries and improve continence and quality of life after delivery.
How similar studies have gone: Previous similar training approaches in obstetrics have shown potential benefits in reducing perineal trauma, but evidence remains limited and context-specific.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years * Provision of written informed consent * Primiparity * Singleton pregnancy * Gestational age ≥ 36 + 0 weeks at the time of delivery * Vaginal delivery, including spontaneous, forceps-assisted, or vacuum-assisted births * No history of anorectal disease and no prior anal or rectal surgery Exclusion Criteria: * Multiparity * Premature delivery * Twin pregnancy * Any preexisting anorectal disease * Preexisting urinary and/or anal incontinence before pregnancy
Where it's running
-
University Hospital Hradec Kralove
Hradec Králové, Czechia Recruiting
Study contacts
- Study coordinator: Dominik Habes, MD
- Email: dominik.habes@seznam.cz
- Phone: +420732545650
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.