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Effect of Virtual Reality Glasses Application on Surgical Fear and Anxiety

U

Uskudar University

Status

Not yet enrolling

Conditions

Fear
Surgery
Virtual Reality
Anxiety State

Treatments

Other: classical training
Other: virtual reality glasses application

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Purpose and Type of Research:This study will be conducted to examine the effect of virtual reality glasses on surgical fear and anxiety in patients scheduled for cardiovascular surgery. The study is a randomized controlled experimental research.

Method:The population of the research was approximately 2900 patients who underwent cardiovascular surgery in a year at Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Education Research Hospital. The sample size of the study was calculated using the G*Power software program.The study will be completed with 60 people by taking 30 people into the experimental and control groups.Data will be collected with a personal information form, surgical fear scale and state anxiety scale.

Hypothesis of the Research:

H1: Application of virtual reality glasses reduces surgical fear in patients planned for cardiovascular surgery.

H2: Application of virtual reality glasses reduces anxiety in patients scheduled for cardiovascular surgery.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years and over,
  • Those who will undergo open heart surgery,
  • Those who have not had cardiovascular surgery before,
  • No communication problems,
  • Is conscious and able to answer questions and does not have any disorder/disease that affects decision-making ability (dementia, Alzheimer's, etc.),
  • Does not have a psychiatric disease such as anxiety disorder, panic attack, depression,
  • Individuals who do not receive psychiatric treatment such as antipsychotics/anxiolytics will be included in the study.

Exclusion criteria

  • Being under the age of 18,
  • Not having open heart surgery,
  • Those who have previously undergone cardiovascular surgery,
  • Having communication problems,
  • Those who are unconscious and unable to answer questions Having any disorder/disease that affects decision-making ability (dementia, Alzheimer's, etc.),
  • Having a psychiatric disease such as anxiety disorder, panic attack, depression,
  • Individuals receiving psychiatric treatment such as antipsychotic/anxiolytic will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

VRG
Experimental group
Treatment:
Other: virtual reality glasses application
Other: classical training
control group
Active Comparator group
Treatment:
Other: classical training

Trial contacts and locations

0

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Central trial contact

sabriye gul

Data sourced from clinicaltrials.gov

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