Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06001489

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients awaiting elective cardiac surgery involving a sternotomy
  • 18 years or older
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Education and Assessment

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)

Pre-surgery Assessment

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)

Surgery

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

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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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