Skip to main content
Clinical Trials/NCT06628856
NCT06628856
Completed
N/A

Ex Ante and Interim Evaluation of the Quality of Life of the Piloted Persons, and Cost-efficiency Analysis

Universidad de Burgos1 site in 1 country166 target enrollmentJanuary 7, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Terminal Illness
Sponsor
Universidad de Burgos
Enrollment
166
Locations
1
Primary Endpoint
Qualitative analysis
Status
Completed
Last Updated
last year

Overview

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, 2.5 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.

Registry
clinicaltrials.gov
Start Date
January 7, 2024
End Date
March 7, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • That the direct care worker has a degree as a nursing assistant, dependency care technician, geroculturist or certificate of professionalism.
  • The worker must speak and understand Spanish.
  • The residence must offer service during the day, in the morning or afternoon shift.
  • Workers must have been with the department for more than 4 months.

Exclusion Criteria

  • Workers who work night shift only.
  • Workers on rotating shifts in all departments of the residence.
  • Workers absent at the time of the study due to temporary leave, vacations or other causes.

Outcomes

Primary Outcomes

Qualitative analysis

Time Frame: 5 MONTHS

structured interviews: The coding system for the qualitative information will be carried out using the Atlas-Ti content analysis program. Atlas-Ti allows exporting a matrix to SPSS format, as a quantitative data matrix composed of the set of ideas, identified by the code of each interview, the idea number and its corresponding code for affected person and family member. In this way, the frequencies of the different categories can be analyzed.

Multilevel analysis

Time Frame: 5 MONTHS

daily records: Multilevel analyses will be performed by applying Mix Models with maximum likelihood (ML) estimation.

Student's t-tests

Time Frame: 5 MONTHS

telematic records: Student's t-tests for independent samples and ANOVAs/ANCOVAs will be applied to analyze differences in the study variables (needs, QOL, coping strategies) according to sociodemographic (sex, age, educational level) and clinical variables (type of disease, type of treatment or dependency status).

Study Sites (1)

Loading locations...

Similar Trials