NCT07483619

Brief Summary

This study investigated whether virtual reality (VR) can reduce pain and anxiety in patients undergoing coronary angiography. Coronary angiography is a common cardiac procedure performed under local anesthesia while patients remain awake, which can cause significant pain and anxiety. Adult patients scheduled for elective coronary angiography were randomly assigned to two groups: one group watched a nature-themed VR video during the procedure, while the control group received standard care. Pain and anxiety levels were measured before and after the procedure using validated scales. The findings of this study may help healthcare providers offer a simple, non-pharmacological method to improve patient comfort during coronary angiography.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2022

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2023

Completed
3.1 years until next milestone

First Submitted

Initial submission to the registry

March 16, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 19, 2026

Completed
Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

1.1 years

First QC Date

March 16, 2026

Last Update Submit

March 16, 2026

Conditions

Keywords

Virtual realityCoronary AngiographyPain ManagementAnxietyNon-pharmacological InterventionRandomized Controlled Trial

Outcome Measures

Primary Outcomes (1)

  • Pain Intensity Measured by Visual Analog Scale (VAS)

    Pain was assessed using the Visual Analog Scale (VAS), a 10-cm horizontal scale where 0 indicates no pain and 10 indicates the worst imaginable pain.

    Measured before and immediately after the coronary angiography procedure

Secondary Outcomes (1)

  • State-Trait Anxiety Level Measured by State-Trait Anxiety Inventory (STAI-S)

    Measured before and immediately after the coronary angiography procedure

Study Arms (2)

Virtual Reality Group

EXPERIMENTAL

Participants watched a nature-themed virtual reality video through a VR headset throughout the coronary angiography procedure in addition to standard care.

Device: Virtual Reality Headset

Control Group

NO INTERVENTION

Participants received standard care without any additional intervention during coronary angiography.

Interventions

Participants in the VR group wore a virtual reality headset and watched a pre-selected nature-themed video throughout the coronary angiography procedure. The VR intervention was applied in addition to standard care and was maintained for the entire duration of the procedure.

Virtual Reality Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged 18 years or older
  • Scheduled for elective coronary angiography
  • Conscious and oriented
  • Able to communicate verbally
  • No prior coronary angiography experience
  • Willing to participate and provided written informed consent

You may not qualify if:

  • History of psychiatric disorder or use of psychiatric medication
  • Visual or hearing impairment that would prevent VR use
  • Hemodynamic instability
  • Emergency coronary angiography
  • Inability to complete the questionnaires
  • Prior experience with virtual reality

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Koç University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety DisordersPainAgnosia

Condition Hierarchy (Ancestors)

Mental DisordersNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsPerceptual DisordersNeurobehavioral ManifestationsNervous System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

March 16, 2026

First Posted

March 19, 2026

Study Start

January 1, 2022

Primary Completion

February 1, 2023

Study Completion

February 1, 2023

Last Updated

March 19, 2026

Record last verified: 2026-03

Locations