Virtual Reality in Elective Caesarean Births Study (VREC)

Recruiting N/A Interventional Study
Anxiety Pregnancy Pain
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
40 (estimated)
Sponsor
Royal United Hospitals Bath NHS Foundation Trust · Other
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About This Trial
This study will establish the safety of a known intervention in a novel setting. It will assess how maternal anxiety during the peri-operative period of an elective cesarean section (eCS) is affected by the introduction of a virtual reality (VR) tool. A cesarean section is the most common operation performed in the world. Indeed, locally, we perform approximately 450 eCS annually, equating to 10% …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Have had the decision for elective LSCS by 38 weeks gestation. * Has never had an emergency or elective section previously * Have a procedure planned and performed as a category 4 LSCS (an elective LSCS booked at a time that suits both the woman and obstetric team) * Have use …
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