Virtual Reality in Obstetric Patients
Completed · Not applicable
Conditions studied: Obstetric Pain, Pain
In brief
The purpose of this study is to determine if non-invasive distracting devices (Virtual Reality headset) are more effective than the standard of care (i.e., no technology based distraction) for preventing anxiety and pain scores in women who are undergoing child laboring procedures. The anticipated primary outcome will be a reduction of pregnant females overall anxiety and pain scores before and after such procedure(s), including but not limited to epidural/combined spinal epidural (CSE), IV placement and/or labor.
Key facts
- Study ID
- NCT03495531
- Run by
- Stanford University
- People needed
- 60
- Starts
- 2018-07-03
- Expected to finish
- 2021-03-11
- Last updated by the study team
- 2021-09-27
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Age 18 and over
- Able to consent
- Obstetric patients who had either have a history of, planning to have, or currently having an child laboring related procedures such as IV placement, epidural/CSE placement and/or labor.
You may not qualify if…
- Inclusion Criteria:
- Age 18 and over
- Able to consent
- Obstetric patients who had either have a history of, planning to have, or currently having an child laboring related procedures such as IV placement, epidural/CSE placement and/or labor.
Where it is running
- LPCH/SHC — Stanford, California, United States
Full record on ClinicalTrials.gov
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