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Effect of Virtual Reality on Preoperative Anxiety

M

Mersin University

Status

Completed

Conditions

Preoperative Anxiety

Treatments

Other: VR application group

Study type

Interventional

Funder types

Other

Identifiers

NCT04547322
Gulay Ugras

Details and patient eligibility

About

The aim of this study was to determine the effect of virtual reality (VR) on the preoperative anxietyof patients undergoing colorectal surgery.

Full description

The sample of this study consisted of 86 patients in experimental and control groups. The experimental group received VR application in the preoperative period for 10 minutes. Anxiety level was assessed with the Anxiety Specific to Surgery Questionnaire (ASSQ) and measured with physiological responses of anxiety such as systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate (HR), respiratory rate (RR) and peripheral oxygen saturation (SpO2) before and after VR application.

Enrollment

86 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:The study included

  • conscious,
  • orientated and cooperated patients who could speak and understand Turkish,
  • who had no psychiatric diseases,
  • who were 18 years old and older,
  • who were scheduled for elective colorectal surgery for the first time,
  • who did not take any sedative drugs before surgery, and
  • who gave written and oral permission to participate in the study

Exclusion Criteria:n The study excluded

  • had language problems,
  • underwent emergency surgery,
  • were over 65 years of age and
  • refused to participate in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

86 participants in 2 patient groups

VR application group
Experimental group
Description:
The experimental group received VR application in the preoperative period for 10 minutes.
Treatment:
Other: VR application group
Control group
No Intervention group
Description:
The control group received the routine procedure in the unit clinic where the study was conducted. The routine procedure of the unit includes patients are taken to the operating room on a stretcher and wait on the stretcher in the surgery waiting room until the operation room is prepared.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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