Ignite Creation Date:
2024-05-06 @ 8:00 PM
Last Modification Date:
2024-10-26 @ 3:18 PM
Study NCT ID:
NCT06215131
Status:
RECRUITING
Last Update Posted:
2024-03-15
First Post:
2024-01-10
Brief Title:
Feasibility of Immersive Virtual Reality Dietician Program in Metabolic-dysfunction Associated Steatotic Liver Disease
Sponsor:
Milton S Hershey Medical Center
Organization:
Milton S Hershey Medical Center
Study Overview
Official Title:
Feasibility of Immersive Virtual Reality Dietician Program in Patients with Metabolic-dysfunction Associated Steatotic Liver Disease
Status:
RECRUITING
Status Verified Date:
2024-08
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:
Metabolic-dysfunction associated steatotic liver disease often referred to as fatty liver disease is a leading cause of liver failure Dietary weight loss is a cornerstone of treating fatty liver disease but access to traditional in-person nutritional education is often limited by cost availability and transportation Immersive virtual reality iVR has the potential to not only overcome these barriers but also provide an interactive learning experience such as measuring and preparing foods Therefore the investigators have created and validated an iVR dietician program known as the Immersive Virtual Alimentation and Nutrition IVAN using evidence-informed practices from the Academy of Nutrition and Dietetics
The goal of this project is to translate the IVAN program from human and patient research to practice and community research The investigators plan to accomplish this by performing a randomized clinical trial evaluating the effect of the IVAN program in combination with synchronous audiovideo dietary counseling on self-reported dietary intake and weight compared to in-person counseling Concurrently the investigators will provide a survey assessing implementation outcomes to both groups as well as the dietician at each study visit and crossover the intervention at study completion so all participants assess the IVAN program Additionally the investigators will have clinic health care providers experience the IVAN program and assess implementation outcomes
The goal of this project is to translate the IVAN program from human and patient research to practice and community research The investigators plan to accomplish this by performing a randomized clinical trial evaluating the effect of the IVAN program in combination with synchronous audiovideo dietary counseling on self-reported dietary intake and weight compared to in-person counseling Concurrently the investigators will provide a survey assessing implementation outcomes to both groups as well as the dietician at each study visit and crossover the intervention at study completion so all participants assess the IVAN program Additionally the investigators will have clinic health care providers experience the IVAN program and assess implementation outcomes
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