Using virtual reality to reduce anxiety before bronchoscopy
The Impact of the Therapeutic Virtual Reality Headset on Patient Anxiety in the Waiting Room Before Flexible Bronchoscopy in Vigil
This study tests if using a virtual reality headset can help patients feel less anxious while they wait for a bronchoscopy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier le Mans Academic / other |
| Locations | 1 site (Le Mans) |
| Trial ID | NCT06799806 on ClinicalTrials.gov |
What this trial studies
This study investigates the use of a therapeutic virtual reality headset to alleviate anxiety in patients waiting for a flexible bronchoscopy. The focus is on the waiting period, which is often a source of significant anxiety for patients. By employing virtual reality technology, the study aims to create a calming environment that may help patients feel more relaxed before their procedure. The intervention involves patients using the virtual reality device while they wait for their examination at Le Mans Hospital.
Who should consider this trial
Good fit: Ideal candidates include adult patients scheduled for bronchial fibroscopy at Le Mans Hospital who are able to provide informed consent.
Not a fit: Patients who have a history of epilepsy, psychiatric conditions, or those who are unable to tolerate virtual reality devices may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety levels in patients undergoing bronchial fibroscopy.
How similar studies have performed: Previous studies have shown promise in using virtual reality to reduce anxiety in various medical settings, suggesting potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients with no age or gender restrictions, seen on an outpatient basis at Le Mans Hospital. * In whom bronchial fibroscopy is indicated. * Person affiliated with or benefiting from a social security . * Free, informed and written consent signed by the participant and the investigator (no later than the day of inclusion and before any examination required by the research). * Patient able and willing to answer questionnaires Exclusion Criteria: * Patient refusing to participate in research * Patient who has already undergone bronchoscopy in vigil * Patient premedicated for bronchial fibroscopy (anxiolytic, etc.) * Patients with a history of epilepsy or psychiatric pathology * Patient with vertigo * Patient uncooperative, demented or unable to tolerate headgear. * patient under guardianship or curatorship * Patients suffering from blindness or deafness * Patient with known significant intolerance to screens and/or virtual reality devices * Pregnant, nursing or parturient women * Unscheduled patients: emergencies, etc. * Hospitalized patients
Where this trial is running
Le Mans
- Centre Hospitalier Le Mans — Le Mans, France (Recruiting)
Study contacts
- Principal investigator: Christine PETIT — Centre Hospitalier le Mans
- Study coordinator: Christelle JADEAU
- Email: cjadeau@ch-lemans.fr
- Phone: +332 44 71 07 81
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.