Virtual Reality During Conization of Cervix Uterus Under Local Anesthesia
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- STATUS
- Recruiting
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- End date
- Mar 13, 2024
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- participants needed
- 100
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- sponsor
- Tel-Aviv Sourasky Medical Center
Summary
To evaluate the effectiveness of virtual reality glasses as a distraction technique in the management of acute pain and anxiety during conization of cervix uterus under local anesthesia
Description
A prospective, open-label, randomized control trial in a tertiary university affiliated medical center between March 2021 to March 2023. Overall, 100 women referred for conization of cervix due to cervical dysplasia will be randomly allocated to undergo conization either with the use of virtual reality glasses (study group) or with standard treatment (control group). The primary outcome measures will include self-reported pain, anxiety scores, and vital signs as an indirect measurement of pain and anxiety, including pulse rate (PR) and respiratory rate (RR). Pain and anxiety outcomes will be measured as numeric rating scores.
Details
| Condition | Dysplasia, Cervix |
|---|---|
| Treatment | SootheVR: AppliedVR, Los Angeles, California a head-mounted display |
| Clinical Study Identifier | NCT04742543 |
| Sponsor | Tel-Aviv Sourasky Medical Center |
| Last Modified on | 13 June 2022 |
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