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Effect of Distraction Technique Using the Virtual Reality on Cardiopulmonary Parameters, Level of Pain and Anxiety in Patients after Percutaneous Coronary Intervention

Effect of Distraction Technique Using the Virtual Reality on Cardiopulmonary Parameters, Level of Pain and Anxiety in Patients after Percutaneous Coronary Intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241114063711N1
Enrollment
72
Registered
2024-11-18
Start date
2024-11-25
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Diseases. Atherosclerotic heart disease of native coronary artery with angina pectoris

Interventions

Intervention 1: Intervention group: After percutaneous coronary intervention, the virtual reality headset as part of this protocol. After putting the patient in a semi-fowler and sitting position, th

Sponsors

University of Kerbala
Lead Sponsor
University of Kerbala
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: A patient who was admitted to the hospital following percutaneous coronary intervention. Males and females who are at least eighteen years old. Patients who are open to taking part in the research. Patients with verbal communication skills and intellectual capacity. Individuals without hearing or vision impairments.

Exclusion criteria

Exclusion criteria: Young children under the age of eighteen. Individuals involved in diagnostic catheterization. Individuals with impaired hearing and vision abilities. Patients who experienced hematoma, hemorrhage, arrhythmia, asystole, or other postoperative complications or postponed. Pilot study participants. Patients decline to take part in the trial.

Design outcomes

Primary

MeasureTime frame
The primary outcome variable is the level of pain and anxiety that can be changed based on virtual reality. Timepoint: fifteen minutes after intervention directly. Method of measurement: The Visual analogue scale (VAS) for pain aoutcom.;The primary outcome variable is the level of anxiety that can be changed based on virtual reality. Timepoint: fifteen minutes after intervention directly. Method of measurement: The Visual analogue scale (VAS-A) for anxiety aoutcom.

Countries

Iraq

Contacts

Public ContactAli Hassan Ibrahim Shutnan

University of Kerbala

ah5917079@gmail.com+964 782 342 9547

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026