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.
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 …
Contacts
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