The Effect of Carer Training on Pressure Ulcers in Palliative Patients
1 other identifier
interventional
72
1 country
1
Brief Summary
The aim of this article is to examine the effect of the training of carers caring for palliative care patients on the prevention and management of pressure ulcers. In this context, how the training affects the level of knowledge and practices of the carers will be evaluated. The findings obtained will contribute to improving the quality of patient care by providing strategic recommendations for the improvement of palliative care services.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 25, 2024
CompletedFirst Submitted
Initial submission to the registry
August 20, 2024
CompletedFirst Posted
Study publicly available on registry
August 22, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2025
CompletedMarch 12, 2025
March 1, 2025
2 months
August 20, 2024
March 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pressure Wound Knowledge Test
CBRT is a 3-point Likert type (true, false, don't know) questionnaire consisting of 17 questions prepared by the researchers in line with the literature. Five of the questions in the test were designed to be reverse scored and 12 were designed to be scored normally. The minimum score of the knowledge test is 0 and the maximum score is 17. The KR-20 value of this measurement tool was calculated as 0.80.
2 month
Study Arms (2)
Education group
EXPERIMENTALCaregivers in the experimental group will be given a detailed and planned training programme on pressure sores.
Control group
NO INTERVENTIONInterventions
aregivers in the experimental group will be given a detailed and planned training programme on pressure sores. The trainings will be held in a total of four sessions, with twenty minutes in each session, two weeks apart.
In the first stage of the study, the participants in the experimental and control groups were asked to complete the 'Introductory Information Form' and '' Pressure sore knowledge test' will be completed. In the second stage of the research, no intervention will be made to the caregivers in the control group, and in the last stage of the research, 'Pressure sore knowledge test' will be filled in as post-test data for all participants.
Eligibility Criteria
You may qualify if:
- Over 18 years of age
- Being the sole informal caregiver of the palliative care patient
- Being able to use physical abilities such as sight and hearing
- No cognitive and communication problems
You may not qualify if:
- Palliative care patient is not the only informal caregiver
- Cognitive and communication problems
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Firat Universitylead
Study Sites (1)
Firat University
Elâzığ, Elâzığ, 23119, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fatoş Uncu, PhD
funcu@firat.edu.tr
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- assistant professor
Study Record Dates
First Submitted
August 20, 2024
First Posted
August 22, 2024
Study Start
July 25, 2024
Primary Completion
September 15, 2024
Study Completion
September 15, 2025
Last Updated
March 12, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share