Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06642636
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-10
Brief Title:
ICU-VR Prior to ICU Admission
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Intensive Care Unit-specific Virtual Reality As Preparation for ICU Admission in Lung Transplant Patients
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Rationale A substantial proportion of the Intensive Care Unit ICU survivors develop psychological impairments due to their ICU admission Several interventions to mitigate these impairments have been explored but lack a proper effect Intensive Care Unit-specific Virtual Reality has proven to be potentially effective in treating PTSD and depression-related sequelae in ICU-survivors
Objective To evaluate the contribution in terms of information provision and patients perspectives of ICU-VR to prepare lung transplant patients for their future ICU admission
Study design A monocentre randomized controlled study
Study population Lung transplant patients who are on the waiting list and understand the Dutch language Due to the criteria for lung transplantation these are 18-71 years of age Participants need to have signed the informed consent formular
Intervention The ICU-VR intervention is designed by an interdisciplinary team of intensivists ICU nurses a psychiatrist a psychologist and a former ICU patient to expose patients to the ICU environment while offering treatment- and department-related information During the 12-minute lasting intervention patients experience different facets of ICU treatment and receive information on the ICU environment treatment and workflow The intervention group will receive this treatment during the appointment with the lung transplantation nurse The control group will receive the regular hospital preparation care
Primary endpoints The primary endpoint will be the difference in information provision of the ICU care of lung transplant patients on the waiting list
Objective To evaluate the contribution in terms of information provision and patients perspectives of ICU-VR to prepare lung transplant patients for their future ICU admission
Study design A monocentre randomized controlled study
Study population Lung transplant patients who are on the waiting list and understand the Dutch language Due to the criteria for lung transplantation these are 18-71 years of age Participants need to have signed the informed consent formular
Intervention The ICU-VR intervention is designed by an interdisciplinary team of intensivists ICU nurses a psychiatrist a psychologist and a former ICU patient to expose patients to the ICU environment while offering treatment- and department-related information During the 12-minute lasting intervention patients experience different facets of ICU treatment and receive information on the ICU environment treatment and workflow The intervention group will receive this treatment during the appointment with the lung transplantation nurse The control group will receive the regular hospital preparation care
Primary endpoints The primary endpoint will be the difference in information provision of the ICU care of lung transplant patients on the waiting list
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None