- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05979402
The Effect of Pressure Ulcer Education on the Knowledge Level of the Relatives of the Patients
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
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Lütfiye Nur Uzun, PhD
- Phone Number: +905441088353
- Email: nuruzun53@gmail.com
Study Contact Backup
- Name: Hümeyra Hançer Tok, PhD
- Phone Number: +905446004410
- Email: hancertok@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Sponsor
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
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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