Viewing Study NCT06438380



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06438380
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-31
First Post: 2024-05-27

Brief Title: User Experience of a Telemedicine Platform for the Follow-up of Post Intensive Care Syndrome PICS
Sponsor: Parc Tauli Research and Innovation Institute Foundation
Organization: Parc Tauli Research and Innovation Institute Foundation

Study Overview

Official Title: Experience of Critically Ill Patients in the Use of a Telemedicine Platform for the Follow-up of Post Intensive Care Syndrome PICS After ICU Discharge
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
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: Survivors of critical illness may present with a set of physical emotional and cognitive sequelae known as Post Intensive Care Syndrome PICS These alterations can become chronic over time and significantly affect patients quality of life Therefore follow-up and monitoring of critically ill patients after ICU discharge for example through telemedicine could be essential for the prevention early detection and management of PICS

Our main objective is to evaluate the suitability and user experience of a telemedicine platform from the perspective of critically ill patients This study proposes the participation of ICU survivors in the design and improvement of a telemedicine platform for PICS follow-up through a qualitative approach Participants will test the platform in person three months after discharge from the ICU and then undergo a semi-structured interview to assess their experience The findings derived from this study may contribute to improve both the content and the format of the platform optimizing resources and facilitating the management of post-ICU sequelae which will have a positive impact on the patients recovery process
Detailed Description: None

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