CClinicalTrials.gg
CompletedNCT06458647Updated Jun 22, 2026

The Effect of Video Streaming With Virtual Reality Before Coronary Angiography

An interventional study of Video Streaming with Virtual Reality in Anxiety, Comfort and Patient Satisfaction, sponsored by TC Erciyes University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by TC Erciyes University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Mar 2024, registered Jun 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
74
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Anxiety
  • Comfort
  • Patient Satisfaction
03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's enrollment of 74 is close to the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

TC Erciyes University is the lead sponsor of 341 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
74 participants (actual)

Study arms

  • Experimental
    Intervention group

    Individuals in the intervention group will be shown a video with virtual reality glasses before entering the angiography procedure.

    Other: Video Streaming with Virtual Reality

  • No intervention
    Control group

    No application will be made to the control group before the procedure.

Interventions

  • OtherVideo Streaming with Virtual Reality

    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.

06

What researchers measure

Primary outcomes

  1. Anxiety

    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.

    Time frame: 30 minutes after angiography

Secondary outcomes

  1. Comfort

    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.

    Time frame: 30 minutes after angiography

  2. Patient satisfaction

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

    Time frame: 30 minutes after angiography

07

Study locations

1 site
  • Erciyes University
    Talas, Kayseri 0(553) 310 49 51, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06458647
Lead sponsor
TC Erciyes University
Responsible party
Sevda Korkut (Associate Prof., TC Erciyes University) — Principal investigator
First posted
Jun 13, 2024
Start date
Mar 1, 2024
Primary completion
Mar 1, 2025
Completion
Mar 1, 2025
Last update
Jun 22, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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