Actively Recruiting
The Effects of 360-degree Virtual Reality on Pre-procedural Anxiety in Patients Awaiting Elective Cardiac Surgery Involving a Sternotomy
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-07-10
100
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Patients awaiting elective cardiac surgery involving a sternotomy often experience pre-procedural anxiety, which can lead to increased need for pain medication, higher risk of complications, and longer recovery times. This study evaluates the effects of 360-degree Virtual Reality (VR) patient education on reducing anxiety levels compared to standard education methods. The research focuses on patients aged 18 and older undergoing procedures such as coronary artery bypass grafting, aiming to improve patient well-being by addressing anxiety before surgery. Participants are randomly assigned to one of two groups. The control group receives standard patient education with oral information and an informative flyer during an outpatient visit. The intervention group receives the same standard education plus a 360-degree VR tour using a VR headset to familiarize them with the hospital environment and clinical pathway. Both groups complete validated anxiety questionnaires (Spielberger's State-Trait Anxiety Inventory and Amsterdam Preoperative Anxiety and Information Scale) during the outpatient visit and again one day before surgery upon hospital admission. Throughout the study, researchers measure various outcomes including state and trait anxiety levels, need for information, pre-procedural anxiety, heart rate, and blood pressure at baseline and follow-up visits, as well as heart rate and blood pressure on the day of surgery. The study monitors the impact of VR education on anxiety and physiological indicators, aiming to understand its potential benefits over standard education. Participants' involvement includes completing questionnaires and attending scheduled visits before their surgery.
CONDITIONS
Brief Title
The Effects of 360-degree Virtual Reality on Pre-procedural Anxiety in Patients Awaiting Elective Cardiac Surgery Involving a Sternotomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients awaiting elective cardiac surgery involving a sternotomy
- 18 years or older
You will not qualify if you...
- Under the age of 18
- History of previous cardiac surgery
- (concomitant) aortic surgery
- Cardiac surgery for congenital heart defects
- Hearing or visual impairments
- Language barriers (inability to understand, speak or read Dutch)
- History of severe mental or psychiatric disorders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants receive standard patient education with oral information and an informative flyer. Those in the intervention group additionally watch a 360-degree Virtual Reality tour of their clinical pathway. After this visit, participants complete anxiety and information need questionnaires.
1 visit (in-person)
Duration - 1 day
Participants are admitted to the hospital 1 day prior to surgery to complete anxiety and information need questionnaires again, assessing pre-procedural anxiety levels and vital signs.
1 visit (in-person)
Duration - 1 day
Participants undergo elective cardiac surgery involving a sternotomy.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Academic Medical Center
Amsterdam, North Holland, Netherlands, 1105 AZ
Actively Recruiting
Research Team
S
Sulayman el Mathari, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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