The Effect of Pressure Ulcer Education on the Knowledge Level of the Relatives of the Patients

August 4, 2023 updated by: Lutfiye Nur Uzun, Abant Izzet Baysal University

Effectiveness of Pressure Wound Prevention Training for the Relatives of Palliative Care Patients: A Randomized Controlled Trial

The purpose of this randomized controlled trial, which included pretest and posttest, was to examine the effectiveness of pressure ulcer prevention and care education given to caregivers of patients treated in a palliative care clinic.

The key questions it aims to answer are:

  • Does the routine clinical training given in the palliative care clinic have an effect on the knowledge level of patients' relatives about pressure ulcers?
  • Does the pressure ulcer education given to the relatives of patients treated in the palliative care clinic have an effect on the level of knowledge about pressure ulcers?

Participants will participate in an educational activity on pressure ulcers. Researchers will compare whether pressure ulcer training given to palliative care patient relatives is effective compared to routine service training with lecture, question-answer and presentation method.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

One-to-one interviews will be conducted with the relatives of the patients in the experimental and control groups, and the appropriate time frame for the clinical operation will be determined. Participants will be informed about the study at the time determined jointly with the companions and at the appropriate place for the clinic.

Personal Information Form and Pressure Ulcer Information Test will be distributed and collected as a pre-test to the participants in the control group. The participants in the control group will not receive any educational intervention by the researcher until the day of discharge. This group will receive routine clinical training given only in the hospital. Training of patients and their relatives in clinics continues with the principle of "Do-Watch-Check". This is how nurses conduct their routine clinical training. The Pressure Ulcer Information Test will be distributed and collected as a post-test to the control group on the day of the patients' discharge.

Personal Information Form and Pressure Ulcer Information Test will be distributed and collected as a pre-test to the participants in the experimental group. In addition to the training given to the participants in the experimental group with the routine "Do-Watch-Check" principle in the clinic, face-to-face pressure ulcer training will be given by the researchers on the day of discharge. The presentation about the pressure ulcer will be given by the researchers in two periods of 30 min + 30 minutes using lectures, case studies and question-answer techniques. Opinions were received from three field experts regarding the validity of the training content of the pressure ulcer topic (CGI: 1.00). The Pressure Ulcer Knowledge Test will be redistributed and collected as a final test on the day of discharge after completion of training.

Study Type

Interventional

Enrollment (Estimated)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Those who agree to participate in the study
  • Native Turkish,
  • 18 years and over
  • Able to read and write

Exclusion Criteria:

  • Who refused to participate in the study
  • Native language is not Turkish
  • Illiterate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Training group
Face-to-face pressure ulcer training will be given to the relatives of the patients in the training group in the determined common time period. The presentation and pressure ulcer content prepared during the trainings will be conveyed by the researcher in two 30-minute sessions using lectures, example events and question-answer techniques.
Face-to-face presure ulcer training
Active Comparator: Control group
Participants in the control group will not be interfered with by the researcher during the research. They will receive routine in-clinic training given by nurses.
No intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pressure ulcer information of palliative care patients' relatives: First test
Time Frame: Just before training
"Pressure Ulcer Knowledge Test" is a test prepared by researchers in line with the literature and sent to three expert academicians to ensure content validity. Pressure Ulcer Knowledge Test is a 3-point Likert-type questionnaire consisting of 17 questions coded as true, false, I don't know. Five of the questions in the test were designed to be scored reversely and 12 of them were scored straight. The score to be taken from the test is between 0-17. A high score indicates that the relatives of the patients have a high level of knowledge about pressure ulcers, and a low score indicates a low level of knowledge.
Just before training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pressure ulcer information of palliative care patients' relatives: Second test
Time Frame: Immediately after training
"Pressure Ulcer Knowledge Test" is a test prepared by researchers in line with the literature and sent to three expert academicians to ensure content validity. Pressure Ulcer Knowledge Test is a 3-point Likert-type questionnaire consisting of 17 questions coded as true, false, I don't know. Five of the questions in the test were designed to be scored reversely and 12 of them were scored straight. The score to be taken from the test is between 0-17. A high score indicates that the relatives of the patients have a high level of knowledge about pressure ulcers, and a low score indicates a low level of knowledge.
Immediately after training

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lütfiye Nur Uzun, PhD, Bolu Abant İzzet Baysal University Faculty of Health Sciences Nursing Department
  • Principal Investigator: Hümeyra Hançer Tok, PhD, Bolu Abant İzzet Baysal University Faculty of Health Sciences Nursing Department

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

August 10, 2023

Primary Completion (Estimated)

August 30, 2023

Study Completion (Estimated)

September 30, 2023

Study Registration Dates

First Submitted

July 30, 2023

First Submitted That Met QC Criteria

August 4, 2023

First Posted (Actual)

August 7, 2023

Study Record Updates

Last Update Posted (Actual)

August 7, 2023

Last Update Submitted That Met QC Criteria

August 4, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AIBU-HEM-UZUN-004

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No IPD will be shared with other researchers.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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