Visual Biofeedback Through Transperineal Ultrasound During the Expulsive Phase of Labour to Improve Maternal Childbirth Satisfaction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorUniversitaire Ziekenhuizen KU Leuven

About this trial

Childbirth is generally regarded as a positive life-changing experience. Up to 44% of women may however experience this as a traumatic event, with 3% suffering from post-traumatic stress disorder after childbirth. The aetiology of a traumatic childbirth experience is a complex interplay between pre-birth, intra-partum and postnatal factors. Feelings of loss of control, lack of interaction with the obstetric caregiver and lack of emotional or practical support during labour are important contributing factors. This trial aims to investigate the effect of providing Visual Biofeedback (VB) through Trans-Perineal Ultrasound (TPU) during the active 2nd stage of labour on maternal childbirth satisfaction. The hypothesis is that the intervention will improve patient-caregiver communication and enhance parturient women's sense of control and empowerment, ultimately improving the birth experience.

Eligibility criteria

Qualifiers

Voluntary written informed consent of the participant.

Term (37-42w) singleton gestations.

Vaginally nulliparous (no previous vaginal birth > 20 weeks of gestation).

Fetus in cephalic presentation, without any major congenital or chromosomal anomalies.

Disqualifiers

Significant psychiatric comorbidity (psychiatric follow-up during pregnancy, or active (psycho-pharmacological) treatment).

History of severe PFDs/surgery (or any other condition affecting pelvic floor function/anatomy, besides pregnancy and delivery).

Significant neurological disease e.g., spinal injury, multiple sclerosis, diabetic neuropathy, etc.

Significant connective tissue disorders (e.g., Ehlers-Danlos syndrome).

Trial design

Treatments tested in this trial

  • visual biofeedback through trans-perineal ultrasound

Treatment groups

488 Participants
are divided into 2 treatment groups