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

Sponsor
Abant Izzet Baysal University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05979402
Collaborator
(none)
70
2
1.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Training group Face-to-face pressure ulcer training
  • Other: Control group
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study is a randomized controlled study with experimental and control groups consisting of pre-test and post-testThis study is a randomized controlled study with experimental and control groups consisting of pre-test and post-test
Masking:
Single (Outcomes Assessor)
Masking Description:
Outcome evaluations will be conducted by a researcher blinded to group allocation.
Primary Purpose:
Other
Official Title:
Effectiveness of Pressure Wound Prevention Training for the Relatives of Palliative Care Patients: A Randomized Controlled Trial
Anticipated Study Start Date :
Aug 10, 2023
Anticipated Primary Completion Date :
Aug 30, 2023
Anticipated Study Completion Date :
Sep 30, 2023

Arms and Interventions

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.

Other: Training group Face-to-face pressure ulcer training
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.

Other: Control group
No intervention

Outcome Measures

Primary Outcome Measures

  1. Pressure ulcer information of palliative care patients' relatives: First test [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.

Secondary Outcome Measures

  1. Pressure ulcer information of palliative care patients' relatives: Second test [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Abant Izzet Baysal University

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 Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lutfiye Nur Uzun, PhD, Abant Izzet Baysal University
ClinicalTrials.gov Identifier:
NCT05979402
Other Study ID Numbers:
  • AIBU-HEM-UZUN-004
First Posted:
Aug 7, 2023
Last Update Posted:
Aug 7, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lutfiye Nur Uzun, PhD, Abant Izzet Baysal University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 7, 2023