Status:

RECRUITING

Evaluation of Virtual Reality to Reduce Anxiety, Pain and Duration of Non-emergency Vigile Bronchial Fibroscopy (AVATAR)

Lead Sponsor:

Assistance Publique - Hôpitaux de Paris

Collaborating Sponsors:

Ministry of Health, France

Conditions:

Respiratory Disorder

Lung Infection

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Bronchial fibroscopy (BF) is a routine practice examination in critical care areas. It can be useful either for the diagnosis of the causal pathology of respiratory distress or for the diagnosis of lu...

Detailed Description

Bronchial fibroscopy (BF) is an invasive examination mainly performed in vigilant patients under local anesthesia very regularly performed in patients hospitalized in critical care. Despite local anes...

Eligibility Criteria

Inclusion

  • Adults (over 18 years of age)
  • Hospitalized in a critical care unit (intensive care and intensive care)
  • Conscious (Glasgow score \>13)
  • Spontaneous ventilation
  • Requiring the realization of a FB
  • First BF during hospitalization
  • Having signed a consent to participate in the study
  • Affiliation to social security

Exclusion

  • Non-French-speaking patient
  • Protected minors or adults who cannot consent to participate
  • People with major neurocognitive impairment
  • Patient refusing to participate in the study
  • Patient on State medical aid
  • Patient under guardianship or curatorship or under judicial protection
  • BF for a vital emergency
  • Prior inclusion in the study
  • Pregnant or breastfeeding women
  • Presence of a tracheostomy or tracheostomy
  • Participation in other intervention research
  • Epilepsy
  • Visual impairment (blindness) or severe hearing impairment (hearing loss, deafness) that does not allow the use of the helmet
  • Psychiatric pathologies such as delusional disorders, hallucinations or schizophrenia.
  • Autism spectrum disorders
  • Patient sensitive to motion sickness
  • Refractory migraine under treatment

Key Trial Info

Start Date :

October 19 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 26 2025

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT05973201

Start Date

October 19 2023

End Date

October 26 2025

Last Update

December 4 2024

Active Locations (5)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 2 (5 locations)

1

CHI Aix en Provence

Aix-en-Provence, France, 13100

2

CHU Dijon

Dijon, France, 21079

3

Hôpital Le Kremlin Bicêtre

Le Kremlin-Bicêtre, France, 94270

4

Hôpital européen Georges Pompidou - AP-HP

Paris, France, 75015