The Effect of Perineal Care Education on Palliative Care Patient' Relatives

July 29, 2023 updated by: Lutfiye Nur Uzun, Abant Izzet Baysal University

The Effect of Training on Perineal Care of Palliative Care Patients With Incontinence on the Knowledge Level of Relatives: A Randomized Controlled Study

The aim of this randomized controlled study, which includes pre-test and post-test, is to examine the perineum care education given to caregivers of patients with incontinence and being treated in a palliative care clinic.

The basic question it aims to answer is:

Does the perineum care training given to the relatives of patients treated in the palliative care clinic have an effect on the level of knowledge about perineum care?

Participants will participate in a training activity on perineum care. Researchers will compare whether perineum care training given to relatives of palliative care patients is effective compared to the routine service operation, by using lecture, question-answer and presentation method.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

A time period suitable for the clinic, patient and companion will be determined by making one-to-one interviews with the companions in the experimental and control groups. Care will be taken to make the applications outside of treatment, visit, care, meal and visitor hours. Accompanying attendants will be met at the specified time and information about the work will be given.

Participants in the control group will be given a Personal Information Form and a Perineum Care Knowledge Test as a pre-test and will be given sufficient time to complete them. The participants in the control group will not be interfered with by the researcher during the research. At the end of the same day, the Perineum Care Knowledge Test will be redistributed and collected as a posttest to the control group. This group will only receive routine nursing training given in the hospital. In palliative care clinics, nurses provide information to patients and their families to help patients maintain their independence and control and make choices during their daily care. In addition, trainings are planned for the needs of the patient and his family. After the research process is completed, a handbook on perineal care will be distributed to the participants in the control group by the researcher.

The participants in the experimental group will be given a Personal Information Form and a Perineum Care Knowledge Test as a pre-test and will be given sufficient time to fill them out. Face-to-face and one-to-one perineal care training will be given to the participants in the experimental group. During the trainings, the presentation prepared in the power point program and the content of perineum care will be conveyed by the researcher in two 30-minute sessions using plain lecture, case study and question and answer techniques. These techniques used are considered to be effective methods in the education of patients and their relatives. Opinions were received from three field experts regarding the content validity of the content of perineal care (CGI: 1.00). The Perineum Care Knowledge Test will be redistributed and collected as a posttest upon completion of the training.

Study Type

Interventional

Enrollment (Estimated)

84

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:

  • Who agreed to participate in the study
  • Hhose mother tongue is Turkish,
  • 18 years old 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 perineal care training will be given to the relatives of the patients in the training group in the determined common time period. During the trainings, the presentation prepared in the power point program and the content of perineum care will be conveyed by the researcher in two 30-minute sessions using plain lecture, case study and question and answer techniques.
Face-to-face perineal care training
Active Comparator: Control group
The participants in the control group will not be interfered with by the researcher during the research.
No intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Palliative care patient relatives' perineum care information: First test
Time Frame: Just before training
"Perineum Care Knowledge Test" is a test prepared by researchers in line with the literature and sent to an expert academician to ensure content validity. The Perineum Care Knowledge Test is a 3-likert-type questionnaire consisting of a total of 15 questions coded as true, false, I don't know. The minimum score to be obtained from the test is 0 and the maximum score is 15. A high score at the end of the evaluation indicates that the relatives of the patients have a high level of knowledge about perineal care, while a low score indicates a low level of knowledge.
Just before training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perineal care information of palliative care patient relatives: Second test
Time Frame: Immediately after training
"Perineum Care Knowledge Test" is a test prepared by researchers in line with the literature and sent to an expert academician to ensure content validity. The Perineum Care Knowledge Test is a 3-likert-type questionnaire consisting of a total of 15 questions coded as true, false, I don't know. The minimum score to be obtained from the test is 0 and the maximum score is 15. A high score at the end of the evaluation indicates that the relatives of the patients have a high level of knowledge about perineal care, while 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 15, 2023

Primary Completion (Estimated)

September 15, 2023

Study Completion (Estimated)

October 15, 2023

Study Registration Dates

First Submitted

July 18, 2023

First Submitted That Met QC Criteria

July 24, 2023

First Posted (Actual)

July 25, 2023

Study Record Updates

Last Update Posted (Actual)

August 1, 2023

Last Update Submitted That Met QC Criteria

July 29, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • AIBU-HEM-UZUN-003

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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