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Using Virtual Reality (VR) Technology in Gynecological and Obstetrics Procedures

NCT05941390 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2023-08-03

No results posted yet for this study

Summary

A randomized control trial will be conducted in Assuta Ashdod hospital, in the department of obstetrics and gynecology. Pregnant and non pregnant women, undergoing one of the procedures (external cephalic version,amniocentesis or hysteroscopy), will be approached. All willing patients meeting the criteria will sign an informed consent form will.

After signing informed consent patients will be randomly allocated into three groups:1) control (no use of VR). 2) use of VR googles without positive psychology. 3) use of VR googles with positive psychology.

Before and after the procedure each group will answer pain and anxiety questionnaires. In addition, following, following each procedure, salivary cortisol levels will be measured.

Conditions

Interventions

DEVICE

VR without positive psychology

Using VR goggles showing relaxing short videos without sound

DEVICE

VR with positive psychology

Using VR goggles showing relaxing short videos with positive psychological messages

Sponsors & Collaborators

  • Assuta Ashdod Hospital

    lead OTHER

Principal Investigators

  • Noa glick fishman, MD · Assuta Ashdod

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-01
Primary Completion
2024-09-01
Completion
2024-09-01

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05941390 on ClinicalTrials.gov