Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06799806

The Impact of the Therapeutic Virtual Reality Headset on Patient Anxiety in the Waiting Room Before Flexible Bronchoscopy in Vigil

Led by Centre Hospitalier le Mans · Updated on 2025-03-24

80

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Bronchial fibroscopy is a frequently used procedure in the management of pneumology patients, and can be a source of anxiety, particularly while waiting for the examination. Investigator's professional experience has shown us that many patients are anxious in the waiting room before a flexible bronchoscopy in vigile. A great deal of research has been carried out into the use of virtual reality to reduce anxiety and pain during care but shortly before bronchoscopy. The innovative aspect is to target the patient's waiting time for the examination. Waiting is a highly anxiety-provoking time, and nurses play a vital role in supporting patients.

CONDITIONS

Official Title

The Impact of the Therapeutic Virtual Reality Headset on Patient Anxiety in the Waiting Room Before Flexible Bronchoscopy in Vigil

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients with no age or gender restrictions, seen on an outpatient basis at Le Mans Hospital
  • Patients for whom bronchial fibroscopy is indicated
  • Persons affiliated with or benefiting from social security
  • Free, informed, and written consent signed by the participant and investigator before any study examination
  • Patients able and willing to answer questionnaires
Not Eligible

You will not qualify if you...

  • Patients refusing to participate in the research
  • Patients who have already undergone bronchoscopy in vigil
  • Patients premedicated for bronchial fibroscopy (e.g., anxiolytics)
  • Patients with a history of epilepsy or psychiatric pathology
  • Patients with vertigo
  • Patients who are uncooperative, demented, or unable to tolerate headgear
  • Patients under guardianship or curatorship
  • Patients suffering from blindness or deafness
  • Patients with known significant intolerance to screens or virtual reality devices
  • Pregnant, nursing, or parturient women
  • Unscheduled patients such as emergencies
  • Hospitalized patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Le Mans

Le Mans, France, 72000

Actively Recruiting

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Research Team

C

Christelle JADEAU

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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