Viewing Study NCT06424808



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06424808
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-22
First Post: 2024-05-10

Brief Title: Pilot Study for the Validity of a Content-based Information Provision Tool Aimed at Improving the Hospitalization Experience of Liver Transplant Patients
Sponsor: Samsung Medical Center
Organization: Samsung Medical Center

Study Overview

Official Title: Pilot Study for the Validity of a Content-based Information Provision Tool Aimed at Improving the Hospitalization Experience of Liver Transplant Patients
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: The investigators aim to evaluate the improvement of the inpatient experience and the usability of a content-based tool a brochure This involves consolidating video content for inpatients on a single website and providing access to it via QR codes in a brochure format

Patients Considering this as a pilot study the investigators plan to recruit around 30 participants Both the experimental and control groups will receive standard care and information with the experimental group additionally receiving the brochure Random assignment will be used for the experimental and control groups Surveys and interviews will be conducted to assess changes in patient experience and usability before and after providing the brochure

Medical Staff Among the medical staff involved in the liver transplant surgical process researchers will select participants based on their degree of involvement with the intervention subjects After obtaining their consent interviews will be conducted concerning patient experiences and the brochure
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