Vırtual Reality and Music in Coronary Angiography

NCT ID: NCT07117838

Last Updated: 2025-09-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-08

Study Completion Date

2024-12-02

Brief Summary

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"Coronary The scope of this study, which was conducted for the purpose of "Distracting Interventions on Patients' Anxiety, Pain and Physiological Parameters During Angiography: The Effect of Virtual Reality and Music", is to help patients at the level of evidence during coronary angiography and to contribute to the literature.

Detailed Description

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Before starting the application, patients who meet the criteria for inclusion in the study will be determined according to the randomization order and information about the study will be given.

Patients will be randomly assigned to the control and intervention groups (virtual reality and music group). Then, the following interventions will be applied sequentially, depending on the group the patient is included in.

After the appropriate participants are determined, written informed consent will be given to the participants and the Patient Introduction Form, State Anxiety Scale and Visual Comparison Scale will be applied just before the procedure begins, and then the patient's physiological parameters will be measured and recorded in the Patient Monitoring Form. Later patients will undergo coronary angiography. For the control group, conventional procedures will be applied by the researcher and medical care staff.

Patients in the virtual reality group, one of the intervention groups, will be shown a video with predetermined relaxing visuals and sounds through virtual reality glasses. Before watching the video, the researcher informed about the use of virtual reality glasses.

The patient will be informed. They will use the SG glasses for 3-5 minutes before the procedure begins for the patient to get used to it, and then the procedure will begin. VR glasses will be kept on throughout the procedure. In addition, the patient is advised at any stage of the application.

He will be told that he can remove his glasses and withdraw from the study. USB MP3 players and headphones will be provided by the researcher to collect data for the music group. Various styles of music (Classical World Music, Popular Music, Classical Turkish Music, Sufi Music) will be loaded into the USB MP3 player. Patients will be able to choose any of these music styles from the folder and listen to them. Music group patients from the intervention groups will be informed before starting the procedure and will be given 3-5 minutes.

MP3 reader and headphones will be provided throughout. Then, the patient will be taken to the coronary angiography procedure and will be allowed to listen to the previously prepared music of the patient's choice throughout the procedure.

Physiological parameters of patients during coronary angiography will be measured. After the procedure is completed, the Patient Introduction Form, State Anxiety Scale and Visual Comparison Scale will be applied to the patients in all three groups, and then the patient's physiological parameters will be measured and recorded in the Patient Monitoring Form.

Conditions

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Virtual Reality Nursing Caries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

One count for 120 patients who met the study's inclusion criteria A list will be created and patients will be distributed to experimental and intervention groups with a computerized randomization program (https://www.random.org/integer-sets/). According to the randomization result, patients will be assigned to the virtual reality group (intervention 1), the music group (intervention 2) and the control group (Control) with standard treatment. All patients will be randomized to the intervention and control groups after being admitted to the angiography unit. - It will be named as intervention group (the group to which virtual reality glasses and music will be applied) and - Control group (the group to which no additional procedure will be applied to the standard care during the coronary angiography procedure).
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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virtual reality

Patients were fitted with virtual reality glasses.

Group Type EXPERIMENTAL

virtual reality

Intervention Type OTHER

Virtual reality application were applied to patients during coronary angiography.

music

Patients were listened to music

Group Type EXPERIMENTAL

music

Intervention Type OTHER

Patients will listen to music during coronary angiography.

control

Patients were not interfered with and were receive standard care.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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virtual reality

Virtual reality application were applied to patients during coronary angiography.

Intervention Type OTHER

music

Patients will listen to music during coronary angiography.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Between the ages of 18-70, Patients who agreed to participate in the study voluntarily, Open to communication, Knows how to read and write, Patients without visual or auditory impairments, Patients who underwent femoral artery area intervention, Patients who are administered opioid and tranquilizer derivative drugs, Patients who were undergoing coronary angiography for the first time were included in the study.

Exclusion Criteria

Having difficulty using virtual reality glasses, Patients with headache, nausea and vomiting were not included in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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HARUN ÜNAL

OTHER

Sponsor Role lead

Responsible Party

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HARUN ÜNAL

Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Harun ÜNAL, phd student

Role: STUDY_CHAIR

ataturk universty

Locations

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Van Yuzuncu Yil University

Van, tuşba, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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1476

Identifier Type: -

Identifier Source: org_study_id

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