Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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.

More Quality of Life (QOL) trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment380 (estimated)
SponsorUniversity Hospital Hradec Kralove
Academic / other
Locations1 site (Hradec Králové)
StatusRecruiting
StartedJuly 1, 2025
Main results expectedNovember 2026
Study endsJanuary 2027
Registry record updatedOctober 8, 2026
Trial IDNCT07865065 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.