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Completed

NCT Number: NCT06458647

The Effect of Video Streaming With Virtual Reality Before Coronary Angiography

This study was planned as a randomized controlled experimental study to examine the effects of virtual reality video on anxiety, comfort and patient satisfaction before coronary angiography. Data will be collected using the Descriptive Characteristics Questionnaire, State-Trait Anxiety Inventory, Early Postoperative Comfort Scale, Visual Analog Scale (VAS) for patient satisfaction and pain, Vital Signs Follow-up Form and Complication Follow-up Form.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Erciyes University

Talas, Kayseri, 0(553) 310 49 51, Turkey (Türkiye)

About this study

This study was planned as a randomized controlled experimental study to examine the effects of virtual reality video on anxiety, comfort and patient satisfaction before coronary angiography. Data will be collected using the Descriptive Characteristics Questionnaire, State-Trait Anxiety Inventory, Early Postoperative Comfort Scale, Visual Analog Scale (VAS) for patient satisfaction and pain, Vital Signs Follow-up Form and Complication Follow-up Form. In addition to the standard practices of the clinic, individuals in the intervention group will be shown a video with virtual reality glasses before entering the angiography procedure. Only standard practices of the clinic will be applied to the control group.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Can speak and understand Turkish,
  • Over 18 years of age,
  • No previous angiography procedure,
  • Oriented to place and time,
  • No psychiatric illness,
  • Not taking any sedative medication,
  • No vision and hearing problems,
  • Patients who volunteered to participate in the study will be included.

Exclusion criteria

  • Patients with any pain or chronic pain prior to coronary angiography,
  • Patients diagnosed with anxiety,
  • Patients with pacemakers,
  • Patients requiring emergency angiography,
  • Patients taking antihistamines and psychiatric drugs,
  • Patients who did not volunteer to participate in the study,
  • Patients taking tranquilizers or pain medication up to 5 hours before the angiography procedure were excluded.

Treatment and study plan

Video Streaming with Virtual Reality

Other

In the study, patients in the intervention group will be watched videos of natural landscapes such as mountains, beaches and waterfalls with virtual reality goggles before the angiography procedure.

Primary outcomes

  1. Anxiety

    Time frame: 30 minutes after angiography

    This inventory, which consists of a total of 40 items, is analyzed in two separate sections: The first part is the State Anxiety Inventory, which consists of 20 items, and the individual answers this section with his/her current feelings. The second part is the Trait Anxiety Inventory, which also consists of 20 items, and the individual answers this section with the feelings they have felt in the last 7 days.

Secondary outcomes

  1. Comfort

    Time frame: 30 minutes after angiography

    The scale, which is based on the concept of comfort, consists of a total of 24 items, 12 of which question the comfort status of the individual before and after the surgical intervention, 12 of which question positive and 12 of which question negative experiences.

  2. Patient satisfaction

    Time frame: 30 minutes after angiography

    Patients will be asked to rate their satisfaction with the intervention on a 10-point scale.

Sponsors and collaborators

Lead sponsor

TC Erciyes University

Other

Registry information

Official study title

Effect of Virtual Reality Video Viewing Before Coronary Angiography on Anxiety, Comfort, and Patient Satisfaction

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jun 13, 2024
Registry last updated
Jun 22, 2026

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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