The Effect of Video Streaming With Virtual Reality Before Coronary Angiography

Anxiety Clinical Trial

Official title:

The Effect of Video Streaming With Virtual Reality on Anxiety, Comfort and Patient Satisfaction Before Coronary Angiography

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06458647
• Other study ID #: 2023/581
• Status: Not yet recruiting
• Phase: N/A
• Start date: July 1, 2024
• Est. completion date: December 15, 2024

Study information

• Verified date: June 2024
• Source: TC Erciyes University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 74
• Est. completion date: December 15, 2024
• Est. primary completion date: October 15, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Anxiety
• Anxiety Disorders
• Comfort
• Patient Satisfaction

Intervention

Other:
• 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.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
TC Erciyes University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Anxiety	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.	30 minutes after angiography
Primary	Comfort	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.	30 minutes after angiography
Primary	Patient satisfaction	Patients will be asked to rate their satisfaction with the intervention on a 10-point scale.	30 minutes after angiography