The Effect of Video Streaming With Virtual Reality Before Coronary Angiography

Not Applicable

Not yet recruiting

• Conditions: Comfort; Patient Satisfaction; Anxiety
• Interventions: Other: Video Streaming with Virtual Reality

• Registration Number: NCT06458647
• Lead Sponsor: TC Erciyes University

Brief 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.

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.

Study Timeline

• Status Verified: 2024-06
• Study First Submitted: 2024-06-09
• Study First Submitted QC: 2024-06-09
• Last Update Submitted: 2024-06-09
• Study First Posted: 2024-06-13
• Last Update Posted: 2024-06-13
• Study Start: 2024-07-01
• Primary Completion: 2024-10-15
• Study Completion: 2024-12-15

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 74

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention group	Video Streaming with Virtual Reality	Individuals in the intervention group will be shown a video with virtual reality glasses before entering the angiography procedure.

Primary Outcome Measures

Name	Time	Method
Patient satisfaction	30 minutes after angiography	Patients will be asked to rate their satisfaction with the intervention on a 10-point scale.
Anxiety	30 minutes after angiography	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.
Comfort	30 minutes after angiography	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.