Viewing Study NCT06442254



Ignite Creation Date: 2024-06-16 @ 11:50 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06442254
Status: COMPLETED
Last Update Posted: 2024-06-04
First Post: 2024-05-01

Brief Title: The Effects of Virtual Reality in Intensive Care Patients
Sponsor: Istinye University
Organization: Istinye University

Study Overview

Official Title: Examining the Effects of Virtual Reality on Early Vital Variables and Spillovers in Intensive Care Patients
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Weakness of respiratory muscles delays weaning from the ventilator prolongs hospital stay and increases treatment costs Conventional treatments for respiratory muscles reverse these negative effects İntensive care services are a set of services that have a very important place in public health care due to the vital support and they provide to all critically ill patients This care services are constantly improving with the use of technological innovations With the development of technology virtual reality application has begun to be used therapeutically in the field of physiotherapy Virtual reality is the combination of reality and imagination with fictions created using technology Today developers can surprisingly create realistic worlds filled with artificial intelligence that behaves believably Studies have shown positive effects of virtual reality on acute respiratory frequency pain and fatigue and in light of this it was predicted that it would be beneficial to apply to intensive care patients This study will shed light on the rehabilitation of patients in intensive care and contribute to the literature
Detailed Description: In the study it was aimed to benefit from the effects of virtual reality application in intensive care patients and have a positive effect on vital signs and respiratory parameters in the early period

This study will be randomly divided into two groups and it is planned to include 17 partipitants in each group The first group will receive only conventional treatment and the second group will receive virtual reality application in addition to conventional treatment To evaluate the effectiveness of the application vital signs respiratory muscle strength grip strength blood gas analysis shortness of breath and fatigue will be evaluated Additionally Richmond Agitation Sedation Scale RASS Nonverbal Pain Scale Glaskow coma scale Physical Function Test in Intensive Care PFIT-CPax Chelsea Critical Care Physical Assessment Tool scales will be used All evaluations will be made before and after the application and a comparison will be made between the two groups

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None