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Completed

NCT Number: NCT05459246

The Effect of Virtual Reality Application on Pain Severity, Anxiety Level and Patient Satisfaction

In this study; It is aimed to examine the Effect of Virtual Reality Based Relaxation Program on Pain Severity, Anxiety Level and Patient Satisfaction in Patients Who Will Be Applied Angiography.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Istanbul Sabahattin Zaim University, Faculty of Health Sciences

Istanbul, Güneydoğu Anadolu Bölgesi, 21076, Turkey (Türkiye)

About this study

Beginning 1 minute before the start of the procedure, the patients will be watched (30-45 minutes) with an android mobile phone inserted into the Cardboard Super Flex Binoculars Glasses, with a music background, licensed product "Secret Garden", during the procedure (30-45 minutes).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being over 18 years old
  • Ability to communicate adequately
  • Absence of psychiatric problems
  • Volunteering to participate in the research
  • Experiencing coronary angiography for the first time

Exclusion criteria

  • Those who have communication problems
  • Those with psychiatric problems
  • Emergency coronary angiography
  • Having symptoms of myocardial infarction,
  • Being unconscious,
  • Having surgery in the last 6 weeks,

Treatment and study plan

Virtual reality glasses

Other

Beginning 1 minute before the start of the procedure, the patients will be watched (30-45 minutes) with an android mobile phone inserted into the Cardboard Super Flex Binoculars Glasses, with a music background, licensed product "Secret Garden", during the procedure (30-45 minutes).

Primary outcomes

  1. Visual Analog Scale

    Time frame: Before angiography (mean 6 months after study completion)

    The patients were asked to mark their level of pain during relaxation or activities on a 10 cm vertical or horizontal line. In addition, there were forms which were numbered from 1-10 or from 1-100. The number 0 is found at the beginning of the line, and the number 10 is located at the end of the line. A value of 0 shows that there is no pain, and the value 10 expresses unendurable pain. GAS is a common scale in the assessment of pain level. A patient is asked to mark the perceived pain on this line, and the marked point is measured in cm.

  2. Visual Analog Scale

    Time frame: After angiography (through study completion, an average of 6 month)

    The patients were asked to mark their level of pain during relaxation or activities on a 10 cm vertical or horizontal line. In addition, there were forms which were numbered from 1-10 or from 1-100. The number 0 is found at the beginning of the line, and the number 10 is located at the end of the line. A value of 0 shows that there is no pain, and the value 10 expresses unendurable pain. GAS is a common scale in the assessment of pain level. A patient is asked to mark the perceived pain on this line, and the marked point is measured in cm.

  3. Anxiety Assessment Scale

    Time frame: Before angiography (mean 6 months after study completion)

    Patients will be asked to show their anxiety levels before and after the procedure on a 10 cm long horizontal line. Line has 0 at the beginning and 10 at the end. 10 means very extreme anxiety and 0 means no anxiety.

  4. Anxiety Assessment Scale

    Time frame: After angiography (through study completion, an average of 6 month)

    Patients will be asked to show their anxiety levels before and after the procedure on a 10 cm long horizontal line. Line has 0 at the beginning and 10 at the end. 10 means very extreme anxiety and 0 means no anxiety.

  5. Physiological Symptoms of Anxiety Follow-up Form

    Time frame: Before angiography (mean 6 months after study completion)

    This form was created by the researcher to record blood pressure, heart rate, respiratory rate and peripheral oxygen saturation (SpO2) value.

  6. Physiological Symptoms of Anxiety Follow-up Form

    Time frame: After angiography (through study completion, an average of 6 month)

    This form was created by the researcher to record blood pressure, heart rate, respiratory rate and peripheral oxygen saturation (SpO2) value.

  7. Virtual Reality Glasses Application Satisfaction Form

    Time frame: Before angiography (mean 6 months after study completion)

    In this form, there are questions prepared in line with the relevant literature in order to determine the satisfaction with the video watched with virtual reality glasses.

  8. Virtual Reality Glasses Application Satisfaction Form

    Time frame: After angiography (through study completion, an average of 6 month)

    In this form, there are questions prepared in line with the relevant literature in order to determine the satisfaction with the video watched with virtual reality glasses.

Sponsors and collaborators

Lead sponsor

Istanbul Sabahattin Zaim University

Other

Registry information

Official study title

The Effect of Virtual Reality Application on Pain Severity, Anxiety Level and Patient Satisfaction in Patients Who Will Be Applied Coronary Angiography

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jul 14, 2022
Registry last updated
Jan 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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