The Effect of Virtual Reality Application Diagnosed With Myocardial Infarction
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: virtual reality glasses.
- Who it may be relevant to
- Registry conditions: Myocardial Infarction. Basic parameters: 18 years — 70 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect of Virtual Reality on Vital Signs and Anxiety in Myocardial Infarction Patients Admitted to Cardiology Intensive Care Unit: A Randomized Controlled Study.
Overview
This study was designed to investigate the effects of VR (virtual reality) glasses on vital signs and anxiety in conscious patients diagnosed with myocardial infarction and admitted to the cardiology intensive care unit.
Detailed description
This study was designed to investigate the effects of VR (virtual reality) glasses on vital signs and anxiety in conscious patients with myocardial infarction (MI) admitted to the cardiology intensive care unit. Studies examining the psychological (anxiety) and physiological (vital signs) effects of VR application on MI patients in cardiology intensive care units are quite limited. In this context, this study aims to examine the effects of VR glasses application on the vital signs (blood pressure, heart rate, SPO2, respiratory rate) and anxiety levels of MI patients in intensive care, within the framework of a randomized experimental design. The data obtained are expected to make significant contributions to the integration of technological interventions into cardiovascular disease management.
Interventions
- Other virtual reality glasses
Participants will be shown a video with nature images through virtual reality glasses, and their vital signs and anxiety levels will be measured.
Primary outcome measures
- Anxiety Level [Time frame: Periprocedural]
- Vital Signs - Blood pressure measurements (SBP, DBP) [Time frame: Periprocedural]
- Vital Signs- heart rate [Time frame: Periprocedural]
- Vital Signs - respiratory rate per minute [Time frame: Periprocedural]
Eligibility criteria
Inclusion criteria
- The patient is in intensive care.
- The patient has been diagnosed with myocardial infarction.
- The patient is between 18 and 70 years old.
- The patient is conscious.
- The patient is oriented and cooperative.
- The patient volunteers to participate in the study.
- The patient is open to communication.
- The patient agrees to participate in the study.
- The patient has no mental, visual, auditory, or speech impairment.
- The patient has undergone stent placement.
- The patient has STEMI.
Exclusion criteria
- The patient has a psychiatric disorder.
- The patient has any communication impairment.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Health services research
Study locations
Turkey (Türkiye) · 1 center
- SBU Van Training and Research Hospital — Van
Identifiers
NCT: NCT07696390 · Myocardial Infarction - VR