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Use Of Virtual Reality To Reduce Anxiety And Pain During Repair Of Perineal Laceration And Episiotomy

Z

Ziv Hospital

Status

Enrolling

Conditions

Perineum; Injury
Episiotomy Wound
Anxiety

Treatments

Device: Virtual Reality for Anxiety Reduction

Study type

Interventional

Funder types

Other

Identifiers

NCT04693013
0103-20-ZIV

Details and patient eligibility

About

Virtual Reality will be used to decrease anxiety and pain during suturing of episiotomy and perineal lacerations

Full description

Perineal lacerations and episiotomies are common after vaginal birth. Surgical repair of these conditions can cause discomfort and anxiety for the post-partum woman.

The purpose of this research is to determine if the use of virtual reality (VR) during repair of a perineal laceration or episiotomy can decrease the anxiety level of the woman. Other parameters that will be measured will be vital signs, time of procedure, and pain level.

84 eligible healthy women after spontaneous or instrumental vaginal birth will be enrolled. Allocation will be randomized by previous sealed envelopes. 42 in the VR group and 42 in the control group. The 42 women in the VR group will have the device placed band in use before the onset of the procedure. Anxiety level will be measured post-procedure by (STAI) State Inventory Anxiety Trait. Pain will be measure by VAS.

Assuming a significant anxiety level of 60% in women undergoing repair of a perineal laceration of episiotomy, in order to demonstrate a reduction to 30% in women using VR with a power of 80% and alpha of 0.05, 42 women will be needed in each group.

Enrollment

84 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Post-partum vaginal delivery, spontaneous or instrumental
  • Episiotomy or 1st or 2nd degree perineal tear
  • informed consent

Exclusion criteria

  • Cesarean delivery
  • 3rd or 4th degree perineal tear
  • no informed consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

84 participants in 2 patient groups

Interventional
Experimental group
Description:
use of virtual reality (VR)
Treatment:
Device: Virtual Reality for Anxiety Reduction
Control
No Intervention group
Description:
no use of VR

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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