The Effect of Video Streaming With Virtual Reality Before Coronary Angiography

NCT ID: NCT06458647

Last Updated: 2024-06-13

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

74 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-01

Study Completion Date

2024-12-15

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Anxiety Comfort Patient Satisfaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Intervention group

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

Group Type EXPERIMENTAL

Video Streaming with Virtual Reality

Intervention Type 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.

Control group

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Video 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.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Sevda Korkut

Associate Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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2023/581

Identifier Type: -

Identifier Source: org_study_id

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