Digital Storytelling-role Play for Ethical Behaviours to Protect Patient Rights and Ethical Sensitivity

May 30, 2025 updated by: Evrim Eyikara, Gazi University

Effect of Digital Storytelling and Role Play on Nursing Students' Ethical Behaviours to Protect Patient Rights and Ethical Sensitivity: A Randomized Controlled Study

This study aimed to investigate the effect of an ethics education using role-play and digital storytelling, on nursing students' ethical behaviours to protect patient's rights and ethical sensitivity.

  • Is role-playing in ethics education effective in improving students' behaviours to protect patients' rights?
  • Is role-playing in ethics education effective in improving students' ethical sensitivity?
  • Is digital storytelling in ethics education effective in improving students' behaviours towards protecting patients' rights?
  • Is digital storytelling in ethics education effective in developing students' ethical sensitivity? The researchers will compare the mean scores of the ethical behaviours toward protecting patient rights scale and ethical sensitivity scale to see whether role-playing and digital storytelling methods in ethics education have an effect on nursing students' ethical behaviours and ethical sensitivity towards protecting patient rights.
  • All groups will participate in the theoretical lectures of ethics education for a total of five weeks, three hours a week.
  • The theoretical lectures will consist of examination of ethics and related concepts, ethical principles, professional values in nursing, relationship between care and ethics, ethical problems and ethical approaches.
  • One week after the theoretical lecture, all groups will participate in a two-week practice phase, three hours a week.
  • Each group will be divided into small groups of 6-7 people.
  • The Intervention I group will conduct an ethical case analysis involving an ethical problem given to them by the researchers in the classroom environment every week and will discuss the analysis using the role-play method in the ethics committee to be formed after the session.
  • Intervention II group will discuss the ethical case analyses with ethical problems written by themselves by coming together outside the classroom environment.
  • Each small group of 6-7 people will present their ethical case analyses to other group members in the classroom through digital storytelling.
  • The control group will continue the standard education.

Study Overview

Study Type

Interventional

Enrollment (Actual)

69

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 Locations

      • Ankara, Turkey, 06500
        • Gazi University Faculty of Nursing

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:

  • First-time registration in the course
  • Being a volunteer

Exclusion Criteria:

  • Non-native speakers of the country's native language
  • Previous graduation from any health-related university

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Role-playing
The role play group will make an ethical analysis of a case involving an ethical problem given to them by the researchers in the classroom environment every week and will discuss the cases using the role play method in the ethics committee to be formed after the session.
The group will analyse the instant cases given by the researchers using the role-play method.
Experimental: Digital storytelling
Digital storytelling group will discuss the ethical analyses of the cases with ethical issues written by themselves outside the classroom environment. Each small group of 6-7 people will present their ethical case analyses to other group members in the classroom through digital storytelling.
The group will analyse the ethical analysis of the cases containing ethical problems written by themselves by using digital storytelling
No Intervention: standard education
The control group will continue the standard education.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean scores of ethical behaviors toward protecting patients'rights
Time Frame: From enrollment to the end of ethics education at 8 weeks.
The mean score will be obtained using the ethical behaviors toward protecting patients'rights scale.
From enrollment to the end of ethics education at 8 weeks.
Mean scores of ethical sensitivity
Time Frame: From enrollment to the end of ethics education at 8 weeks.
The mean score will be obtained using the ethical sensitivity scale.
From enrollment to the end of ethics education at 8 weeks.

Collaborators and Investigators

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

Sponsor

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 (Actual)

November 6, 2024

Primary Completion (Actual)

May 5, 2025

Study Completion (Actual)

May 25, 2025

Study Registration Dates

First Submitted

November 6, 2024

First Submitted That Met QC Criteria

November 6, 2024

First Posted (Actual)

November 7, 2024

Study Record Updates

Last Update Posted (Actual)

May 31, 2025

Last Update Submitted That Met QC Criteria

May 30, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • GaziU-HF-ES-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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