Virtual reality in postoperative acute pain management in thoracic surgery
Résumé de l'étude
We are planning an interdisciplinary exploratory feasibility study at the University Hospital Basel and are exploring the possibility of using virtual reality (VR) glasses for patients after thoracic surgical procedures. We want to find out what effect such a VR headset has on acute pain in hospitalized patients. Current studies suggest that these interventions can reduce pain perception. However, they have not yet been applied to thoracic patients.
(BASEC)
Intervention étudiée
As part of this study, we use a commonly used standard VR headset, through which calming 360° videos can be viewed.
(BASEC)
Maladie en cours d'investigation
Patients after surgery on the chest
(BASEC)
Patients must be over 18 years old, have consented to the study, be able to speak, understand German, and have undergone a video-assisted anatomical lung resection (that is, the surgery lasted at least 90 minutes). (BASEC)
Critères d'exclusion
Patients may not participate if they: - Have significant psychiatric, cognitive, or neurological impairments (delirium, psychoses, unstable dissociative disorders, any form of organic brain disorder, ...) - Are unable to follow the study procedures (e.g., due to language problems, visual and hearing impairments, ...) - Have chronic pain - Have morphine intolerance - Excessive alcohol consumption (men > 3 standard drinks, women > 2 standard drinks per day) - Substance abuse - Are unable or unwilling to sign an informed consent (BASEC)
Lieu de l’étude
Bâle
(BASEC)
Sponsor
Universitätsspital Basel
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Prof. Jens Eckstein
061 328 47 67
jens.eckstein@clutterusb.chUniversitätsspital Basel
(BASEC)
Informations générales
University Hospital, Basel, Switzerland,
+41 61 328 76 89;+41 61 328 76 89
jens.eckstein@clutterusb.ch(ICTRP)
Informations générales
University Hospital, Basel, Switzerland
(ICTRP)
Informations scientifiques
University Hospital, Basel, Switzerland,
+41 61 328 76 89;+41 61 328 76 89
jens.eckstein@clutterusb.ch(ICTRP)
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Ethikkommission Nordwest- und Zentralschweiz EKNZ
(BASEC)
Date d'approbation du comité d'éthique
16.10.2023
(BASEC)
Identifiant de l'essai ICTRP
NCT06097520 (ICTRP)
Titre officiel (approuvé par le comité d'éthique)
Virtual Reality in Postoperative Acute Pain Management in Thoracic Surgery (VRThx) (BASEC)
Titre académique
Virtual Reality in Postoperative Acute Pain Management in Thoracic Surgery (VRThx) (ICTRP)
Titre public
Virtual Reality in Postoperative Acute Pain Management in Thoracic Surgery (ICTRP)
Maladie en cours d'investigation
Postoperative Pain (ICTRP)
Intervention étudiée
Other: VR Intervention (ICTRP)
Type d'essai
Interventional (ICTRP)
Plan de l'étude
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label). (ICTRP)
Critères d'inclusion/exclusion
Inclusion Criteria:
- Patients =18 years
- Written informed consent as documented by signature from the patient
- Video-assisted anatomical resection of the lung (VATS) (Surgery duration of at least
90 minutes)
- Ability to speak, understand and read German
Exclusion Criteria:
- Significant mental, cognitive or neurological impairments (Delirium, psychoses,
unstable dissociative disorders, any form of organic brain disorder, ...)
- Inability to follow the study procedures (e.g., due to language problems, visual and
hearing impairments)
- Chronic pain
- Morphine intolerance
- Excessive alcohol consumption (men > 3 standard drinks, women > 2 standard drinks
per day)
- Substance abuse
- Unable or not willing to sign informed consent (ICTRP)
non disponible
Critères d'évaluation principaux et secondaires
Change in postoperative pain intensity level (ICTRP)
Opioid Consumption (ICTRP)
Date d'enregistrement
18.10.2023 (ICTRP)
Inclusion du premier participant
non disponible
Sponsors secondaires
non disponible
Contacts supplémentaires
Joanna Timiliotis, MSc;Jens Eckstein, Prof. Dr. med.;Jens Eckstein, Prof. Dr. med., jens.eckstein@usb.ch, +41 61 328 76 89;+41 61 328 76 89, University Hospital, Basel, Switzerland, (ICTRP)
ID secondaires
2023-01673, am23Eckstein (ICTRP)
Résultats-Données individuelles des participants
non disponible
Informations complémentaires sur l'essai
https://clinicaltrials.gov/ct2/show/NCT06097520 (ICTRP)
Résultats de l'essai
Résumé des résultats
non disponible
Lien vers les résultats dans le registre primaire
non disponible