Virtual Reality for Patient Preparation Before Cardiac Catheterization in Oman
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 Education.
- Who it may be relevant to
- Registry conditions: Coronary Artery Disease, Ischaemic Heart Desease, Cardiac Catheterization. Basic parameters: from 19 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
- Center list to be confirmed — check the primary protocol.
- 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
Evaluating the Efficacy of Virtual Reality in Patient Preparation for Cardiac Catheterization Procedures in Oman: A Randomized Controlled Trial
Overview
Background: Cardiovascular disease is considered one of the most prevalent diseases in recent times, and cardiac catheterization is widely used to diagnose and treat cardiovascular disease. However, patients often experience significant anxiety before the procedure due to fear of the unknown, potential complications, and concern about discomfort.Aim: To evaluate the efficacy of virtual reality technology to reduce anxiety and improve patient satisfaction, attitude, and usefulness in individuals undergoing first-time cardiac catheterization procedures in Oman.Method: A mixed-method randomized control trial will be used with approximately 120 patients from different tertiary hospitals in Oman. The experimental group will experience a virtual reality simulation of the catheterization process before providing informed consent, while the control group will receive the standard pre-procedure education. The Arabic version of the DASS-21 scale will be used to assess anxiety level pre- and post-intervention, while patient satisfaction will be measured through qualitative interviews with a subset of 10 participants.Result: ANOVA will be conducted to examine differences in anxiety and satisfaction scores between groups, and Pearson's correlation (r) will assess relationships between anxiety levels and satisfaction scores, while paired t-tests will be applied to compare anxiety levels before and after the intervention within groups. Additionally, multiple regression analysis will be employed to identify predictors of patient satisfaction and anxiety reduction, with a significance level set at p ≤ 0.05 for all statistical tests.Conclusion: The expected outcome of this study is that virtual reality-based education will significantly reduce pre-procedure anxiety and enhance patient satisfaction compared to standard education. Findings from this research may contribute to improving patient-centered care and developing innovative strategies to optimize emotional preparedness before cardiac catheterization procedures.
Interventions
- Behavioral Virtual Reality Education
Participants in this group will receive a virtual reality-based educational session prior to their first cardiac catheterization. The VR module provides an immersive 3D orientation to the catheterization process, including admission, preparation, transfer to the Cath Lab, procedural steps, and post-procedure recovery. The VR session lasts approximately 10-15 minutes and is delivered once in a quiet hospital setting before the scheduled procedure. This innovative approach aims to enhance patient
Primary outcome measures
- Change in pre-procedural anxiety (measured by DASS-21 Anxiety Subscale) [Time frame: Baseline (before intervention) to immediately prior to cardiac catheterization (within 24 hours).]
Eligibility criteria
Inclusion criteria
- • Adult patients (aged 18 years and above)
- Scheduled for first-time elective cardiac catheterization
- Able to understand Arabic or English
- Capable of providing informed consent
Exclusion criteria
- • Individuals with cognitive impairment or psychiatric conditions that may interfere with their ability to engage in the VR intervention
- Patients requiring emergency or urgent catheterization
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
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07320248 · 107/2025