NCT06565949

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

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

August 20, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 22, 2024

Completed
24 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2024

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2025

Completed
Last Updated

March 12, 2025

Status Verified

March 1, 2025

Enrollment Period

2 months

First QC Date

August 20, 2024

Last Update Submit

March 11, 2025

Conditions

Keywords

Palliative CarePressure Ulcers

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

EXPERIMENTAL

Caregivers in the experimental group will be given a detailed and planned training programme on pressure sores.

Other: Education groupOther: control group

Control group

NO INTERVENTION

Interventions

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.

Also known as: C
Education group

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.

Education group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Firat University

Elâzığ, Elâzığ, 23119, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Pressure Ulcer

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Skin UlcerSkin DiseasesSkin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Fatoş Uncu, PhD

    funcu@firat.edu.tr

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Fatoş Uncu, PhD

CONTACT

Hasan Evcimen, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: The research will be conducted as a randomised experimental study with pretest-posttest control 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

Locations