Viewing Study NCT06574438



Ignite Creation Date: 2024-10-25 @ 7:51 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06574438
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-25

Brief Title: The Effectiveness of AIFIGA Program on Nursing Home Nursing Staff and Family and ResidentsHealth
Sponsor: None
Organization: None

Study Overview

Official Title: The Effectiveness of Artificial Intelligence Family Involvement Generative Agent AIFIGA Program on Nursing Home Nursing Staff and Family and ResidentsHealth
Status: RECRUITING
Status Verified Date: 2024-05
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: This study aims to develop and evaluate the longitudinal effectiveness of the Artificial Intelligence Family Involvement Generative Agent AIFIGA program in enhancing the health of nursing staff family and residents health through the use of a sequential mixed methods research design The development of a real-time interactive and informative AIFIGA program that sparks innovation is necessary to achieve effective communication between families and nursing staff

In Phase I lasting 18 months we will develop the AIFIGA program based on triangulate research design observation and in-depth interview understanding the daily communication experiences and expectations from both families and nursing staff perception in Nursing HomesNHs after COVID-19 as well as our previous years research results The training data for AIFIGA will be derived from the collection of communication dialogues in these qualitative data Furthermore the intelligence of AIFIGA will be developed using publicly available large language models LLMs

In Phase II spanning the next 18 months we will evaluate the longitudinal effects of the AIFIGA program on the health of residents families and nursing staff tracking changes over time baseline 1 month 3 months and 6 months There will be two groups of participants a an AIFIGA group that receives the AIFIGA program and uses it for 3 months and b a control group that receives only routine care
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