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The Effect of Virtual Reality on Women Undergoing Endometrial Biopsy

O

Ondokuz Mayıs University

Status

Enrolling

Conditions

Endometrial Biopsy

Treatments

Other: Virtual Reality Group

Study type

Interventional

Funder types

Other

Identifiers

NCT06961097
2025/7/4

Details and patient eligibility

About

The aim was to determine the effect of nature sounds and images that will be shown to women who underwent endometrial biopsy by using virtual reality glasses on pain and anxiety.

Hypotheses H0: Virtual reality glasses have no effect on women's pain and anxiety during endometrial biopsy.

H1: Virtual reality glasses have an effect on women's pain and anxiety during endometrial biopsy.

The study will be carried out in two different groups. The practice will start with meeting the women who apply to the Radiology clinic for an endometrial biopsy. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Virtual Reality Group In addition to the routine procedure, virtual reality glasses will be applied to the women in the virtual reality group of the research. Virtual reality glasses is a device that works on compatible smart mobile phones. After being taken to the gynecological table for the HSG procedure, the women included in the experimental group will be made to watch a video lasting an average of 15 minutes with virtual reality glasses until the procedure is completed. While watching the video, the relaxing nature sounds music of the video will be played in the practice room with a bluetooth speaker.

Control Group Patients in the control group of the study will not be subjected to any treatment other than the routine procedure.

Enrollment

64 estimated patients

Sex

Female

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • *Being over 18 years old

    • Speaking and understanding Turkish
    • Being willing to participate in the research

Exclusion criteria

  • Not volunteering to participate in research * Not speaking or understanding Turkish

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

Virtual Reality Group
Experimental group
Description:
In addition to the routine procedure, virtual reality glasses will be applied to the women in the virtual reality group of the research. After being taken to the gynecological table for the endometraial biopsy procedure, the women included in the experimental group will be made to watch a video lasting an average of 15 minutes with virtual reality glasses until the procedure is completed. While watching the video, the relaxing nature sound music of the video will be played.
Treatment:
Other: Virtual Reality Group
control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Sümeyye BAL, Ph.D

Data sourced from clinicaltrials.gov

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