Viewing Study NCT06628856



Ignite Creation Date: 2024-10-25 @ 7:52 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06628856
Status: COMPLETED
Last Update Posted: None
First Post: 2024-02-26

Brief Title: Quality of Life of the Piloted Individuals and a Cost-efficiency Analysis
Sponsor: None
Organization: None

Study Overview

Official Title: Ex Ante and Interim Evaluation of the Quality of Life of the Piloted Persons and Cost-efficiency Analysis
Status: COMPLETED
Status Verified Date: 2024-02
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: The increasing life expectancy and global aging population necessitate changes in long-term gerontological services based on Person-Centred Care approaches This study aims to improve Person-Centred Care in geriatric centers through meaningful activities and the role of occupational therapists and direct care professionals in developing these activities A descriptive cross-sectional quasi-experimental design was proposed with 10 participants
Detailed Description: Background Increasing life expectancy means that the ageing of populations globally is on the rise It is therefore important to promote changes in long-term gerontological services based on Person-Centred Care approaches in which meaningful occupation serves as a basis and is supported by appropriate professional support such as the occupational therapist and the direct care professional

Objective The study aims to analyze the needs quality of life and coping strategies of terminally ill patients over five months as well as burnout and dehumanization among caregivers and healthcare staff

Methods This study examines factors influencing the quality of life QOL of terminally ill patients and the burnout and dehumanization of caregivers and health professionals using a mixed methodology The study proposes a 3-time longitudinal design with evaluations at baseline 25 months and 5 months to measure the impact of an intervention on terminally ill patients and their families focusing on health status quality of life and emotional well-being

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