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Virtual Reality Mindfulness in Preoperative Anxious Patients

Virtual Reality Mindfulness in Preoperative Anxious Patients

Not Recruiting
18 years and older
All
Phase N/A

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Overview

The goal of this interventional study is to reduce preoperative anxiety by Virtual Reality mindfulness.

Population: all adults, able to give their consent and scheduled for surgery with high preoperative anxiety defined by Amsterdam Preoperative Anxiety and Information Scale (APAIS) score > 10. The study will recruit 100 patients in one university teaching hospital.

The main question it aims to answer is: may mindfulness by Virtual Reality reduce preoperative anxiety in patients particularly anxious for the surgery? Participants will be asked to undergo to a single mindfulness virtual reality session before the surgery.

Eligibility

Inclusion Criteria:

  • adults able to give their consent, scheduled for elective surgery and with high preoperative anxiety defined by Amsterdam Preoperative Anxiety and Information Scale (APAIS) > 10

Exclusion Criteria:

  • Pregnancy
  • Epilepsy
  • Pacemaker wearers
  • Mental diseases
  • Alcohol or drug addiction
  • Severe hearing loss or blindness
  • Simultaneous participation to other studies

Study details
    Test Anxiety
    Anxiety State
    Preoperative Period

NCT05860192

Ospedale Regionale di Mendrisio

30 January 2026

FAQs

Learn more about clinical trials

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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