Pleural Effusion, Pneumothorax Spontaneous Primary, Pneumothorax Spontaneous Secondary
Conditions
Keywords
virtual reality, chest drain, pain management, chest tube, anxiety management
Brief summary
Clinical study aiming to investigate the potential benefit of the use of virtual reality helmet as a distractor during chest drain insertion to alleviate patients' pain and anxiety
Interventions
DEVICEVirtual Reality Headset
A virtual reality headset will be placed on patients' head before and during chest drain insertion
Sponsors
Central Hospital, Nancy, France
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Indication of chest drain insertion for pleural effusion or primary spontaneous pneumothorax * Patient who received clear and loyal information abotu the study protocol * Patient who consented to participate to the study * Patient aged 18 years old or older * Patient affiliated to the french health system
Exclusion criteria
* Patient aged less than 18 years old * Patient in emergency situation * Patient with severe heart condition * Patient allergic to silicone * Patient with severe psychiatric or mental disorder * patient with binocular vision anomaly * patient with pacemaker or defibrillator * patient wearing a hearing aid that cannot be removed * Patients under the influence of alcohol or drugs, nausea, fatigue, emotional or anxiety disorders, migraine, headaches, infectious disease * Patient with past medical history of epilepsia or convulsion \-- Persons covered by articles L. 1121-5 and L1121-8 of the French Public Health Code: * Pregnant, parturient or breast-feeding women, * Persons of full age subject to a legal protection measure (guardianship, curatorship, safeguard of justice) * adults unable to give their consent * Persons deprived of their liberty by a judicial or administrative decision, persons under psychiatric care under articles L. 3212-1 and L. 3213-1. * Person able to give consent but unable to write * Person able to give consent but unable to read French * Patient unable to consent to the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain - Chest drain | During chest drain insertion | Visual Analogic Scale |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain - Antalgic consumption | during the 24 hours after chest drain insertion | Antalgic consumption |
| Pain - 30 minutes | 30 minutes after chest drain insertion | Visual Analogic scale |
| Anxiety - Chest drain | During chest drain insertion | Anxiety Visual Analogic Scale |
| Anxiety - 30 minutes | 30 minutes after chest drain insertion | Anxiety Visual Analogic Scale |
| feasibility | During chest drain insertion | Was the chest drain insertion duable with the virtual reality headset |
Contacts
Primary ContactArthur Streit, MD, MSc
Backup ContactJoseph Seitlinger, MD, Phd
Outcome results
None listed