Effect of VR Glasses and Stress Ball on Anxiety in Coronary Angiography Patients

NCT ID: NCT07087990

Last Updated: 2025-07-30

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

105 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-01

Study Completion Date

2025-05-01

Brief Summary

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This randomized controlled trial aimed to evaluate the effects of virtual reality (VR) glasses and the use of a stress ball on anxiety, pain, and satisfaction levels in patients undergoing coronary angiography. Participants were randomly assigned to three groups: one group received both VR and stress ball interventions during the procedure, while the control group received standard care. Anxiety, pain, and satisfaction levels were assessed and compared across the three groups at the conclusion of the procedure. The study seeks to contribute to evidence on non-pharmacological methods to improve patient comfort during invasive cardiac procedures.

Detailed Description

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This randomized controlled trial aimed to evaluate the effects of virtual reality (VR) glasses and the use of a stress ball on anxiety, pain, and satisfaction levels in patients undergoing coronary angiography. Participants were randomly assigned to three groups: one group received both VR and stress ball interventions during the procedure, while the control group received standard care. Anxiety, pain, and satisfaction levels were assessed and compared across the three groups at the conclusion of the procedure. The study seeks to contribute to evidence on non-pharmacological methods to improve patient comfort during invasive cardiac procedures.

Conditions

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Coronary Angiography (CAG) Anxiety Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

randomize kontrollü
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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VR Group"Participants in this group were provided with virtual reality glasses during coronary angio

Participants in this group were provided with virtual reality glasses during coronary angiography to assess the effect on anxiety, pain, and satisfaction.

Group Type EXPERIMENTAL

Virtual Reality Glasses

Intervention Type DEVICE

articipants in the VR group used virtual reality glasses during coronary angiography to reduce anxiety and pain and improve satisfaction.

Stress Ball Group

Participants in this group used a stress ball during coronary angiography to evaluate its effect on anxiety, pain, and satisfaction.

Group Type EXPERIMENTAL

Stress Ball

Intervention Type OTHER

articipants in the stress ball group used a stress ball during coronary angiography to evaluate its effects on anxiety, pain, and satisfaction.

Control Group

Participants in this group received standard care during coronary angiography without the use of virtual reality glasses or stress ball. Anxiety, pain, and satisfaction levels were assessed

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Virtual Reality Glasses

articipants in the VR group used virtual reality glasses during coronary angiography to reduce anxiety and pain and improve satisfaction.

Intervention Type DEVICE

Stress Ball

articipants in the stress ball group used a stress ball during coronary angiography to evaluate its effects on anxiety, pain, and satisfaction.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Voluntary participation in the study
* Age 18 years or older
* Undergoing coronary angiography for the first time
* Cognitive ability to answer the questions
* No diagnosis of anxiety disorder and no use of medication for anxiety / no psychiatric diagnosis
* No physical disability preventing the use of the stress ball
* No problems with vision, hearing, or understanding

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Istanbul Sabahattin Zaim University

OTHER

Sponsor Role lead

Responsible Party

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Rabia Ozdemir

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Zülfünaz Özer, PhD

Role: STUDY_CHAIR

İstanbul Sabahattin Zaim University

Locations

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Istanbul Sabattin Zaim Üniversitesi

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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IZU-EC-2024-10

Identifier Type: -

Identifier Source: org_study_id

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