The Effect of Creative Drama on Postmortem Care in Nursing Students

NCT ID: NCT05661500

Last Updated: 2023-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-11-04

Study Completion Date

2023-03-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The goal of this randomized controlled including pretest, posttest and persistence test study is to examine the effect of creative drama method on student nurses' knowledge and skill levels related to postmortem care, learning permanence and satisfaction with the training method.

The main question it aims to answer are:

•Is the postmortem care training given to nursing students with the creative drama method effective on the level of knowledge and skills, the permanence of knowledge and skills and satisfaction with the training method? Participants will participate in an educational activity related to postmortem care. Researchers will compare it with the classical education method to see if postmortem care training given to nursing students with the creative drama method is effective.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The research will be carried out in the form of determining the preliminary knowledge of nursing third year students about postmortem care, providing education with classical education and creative drama methods, evaluating the educational outcomes and permanence in education for knowledge and skills, and determining their satisfaction with the educational methods.

Hypotheses of the research are as follows. H1: There is a difference between the knowledge scores of the experimental and control groups on postmortem care. Is there a difference between the creative drama method and classical education method and the satisfaction of postmortem care students with the training method? H2: There is a difference between the skill scores of the experimental and control groups for postmortem care. H

: There is a difference between the information persistence scores of the experimental and control groups related to postmortem care.

H4: There is a difference between the skill persistence scores of the experimental and control groups for postmortem care.

H5: There is a difference between the satisfaction of the experimental and control groups with the training method

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Healthy

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This study is a randomized controlled trial with experimental and control groups including pretest, posttest and persistence test.
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors
Outcome assessments will be performed by a investigator who was blinded to group allocation.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Creative Darama Group

Postmortem care content including "The concept of death", "Postmortem Care", "Postmortem Care" and "Postmortem Care Practices" will be given to the students in the Creative Darama group in six sessions consisting of the preparation/warm-up, animation and evaluation stages of creative drama.

Group Type EXPERIMENTAL

Creative Darama Group

Intervention Type OTHER

Postmortem care training given by creative drama method

Classical Education Group

Theoretical training titled "Post-Death Care" and "The Concept of Death", "Post-Death Changes", "Post-Death Care" and "Post-Death Care Practices" will be conveyed to the students in the classical education group by the researcher using the method of direct expression. After the theoretical training, the students will be taken to the application laboratory and post-mortem care applications will be explained with the demonstration method.

Group Type ACTIVE_COMPARATOR

Classical Education Group

Intervention Type OTHER

Postmortem care training given by classical education method

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Creative Darama Group

Postmortem care training given by creative drama method

Intervention Type OTHER

Classical Education Group

Postmortem care training given by classical education method

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Bolu Abant İzzet Baysal University Faculty of Health Sciences, Department of Nursing, 2022-2023 academic year fall semester to be studying in the third year.
* To have taken the "Principles of Nursing" course and the Loss-Death-Mourning process described in this context at the theoretical level.
* Agreeing to participate in the research.

Exclusion Criteria

* Have previously received skills training related to postmortem care.
* Have previous clinical experience with postmortem care.
* Have previously provided postmortem care.
* Not agreeing to participate in the research.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Abant Izzet Baysal University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Lutfiye Nur Uzun

PhD Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Lütfiye Nur Uzun, PhD Student

Role: PRINCIPAL_INVESTIGATOR

Bolu Abant İzzet Baysal University Faculty of Health Sciences Nursing Department

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Bolu Abant İzzet Baysal University Faculty of Health Sciences Nursing Department

Bolu, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AIBU-HEM-UZUN-001

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.