Effect of Reflective Thinking Method on Ethical Decision Making, Professional Values and Compassion Level

November 4, 2024 updated by: Serpil SU, Necmettin Erbakan University

The Effect of Reflective Thinking Method Used in Ethics Teaching on Ethical Decision Making, Professional Values and Compassion Level in Nursing Students

This randomized controlled study aimed to determine the effect of the reflective thinking method used in ethics education on ethical decision making, professional values, and compassion levels in nursing students.The hypotheses of the study are as follows:

H1.1. There is a difference in ethical decision-making average scores between students who were applied the reflection method in ethics education and students in the control group.

H1.2. There is a difference in professional values average scores between students who were applied the reflection method in ethics education and students in the control group.

H1.3. There is a difference in compassion average scores between students who were applied the reflection method in ethics education and students in the control group.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

The research will be conducted as a pre-test-post-test, parallel group randomized controlled experimental design. The sample of the research to be conducted at Necmettin Erbakan University Faculty of Nursing consists of 84 students. Students who meet the inclusion criteria will be assigned to the intervention and control groups by the block randomization method. The intervention group will be given ethics training with the reflective thinking method, while the control group will be given standard ethics training. The research data will be collected between November 22, 2024 and March 31, 2025 using the Student Information Form, Nursing Ethical Dilemma Test, Professional Values Scale and Compassion Scale.

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

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:

  • Being between the ages of 18-65
  • Being registered in the Professional Ethics course
  • Having participated in the theoretical part of the Professional Ethics course
  • Being volunteering to participate in the research

Exclusion Criteria:

  • Having taken the Professional Ethics course before
  • Working as a healthcare professional
  • Being a foreign national

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: Reflective thinking

Discussion sessions will be held once a week for 7 weeks within the scope of the Professional Ethics Course for the students in the intervention group. For the discussion sessions, the students will be divided into 4 groups of 10-11 people. Separate 1-hour discussion sessions will be held with each group.

A training session will be held with the students in the intervention group in the first week (November 22,2024). In this session; the researchers will inform the students about the reflective thinking technique. In the 2nd, 3rd, 4th, 5th, 6th and 7th weeks (January 03, 2025), the students will come to class by writing an event/situation they encountered during their hospital internship in the Obstetrics and Gynecology Nursing course, which they are currently doing clinical practice. During the class hour, the researcher will determine one of the events/situations written by the students and will discuss it in the group.Follow-up data will be collected after 3 months (March 31,2025).

It will be applied to students in the initiative group for 1 hour per week for 7 weeks.
No Intervention: Control
No application will be made to the students in the control group. These students will be given standard education for 7 weeks (Between November 22, 2024 and January 03, 2025).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ethical Dilemma Test to determine the level of ethical decision making
Time Frame: 1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).
The aim of determining the levels of "Principle Thinking" (F) and "Practical Thinking (P) is to determine the situation of encountering an ethical dilemma (Familiarity). The lowest "Principle Thinking" score that can be achieved in the test is 18, the highest "Principle Thinking" score is 66. The lowest "Practical Thinking" score that can be achieved is 6, and the highest "Practical Thinking" score is 36. In the familiarity section, 6-17 points indicate familiarity with a similar dilemma, and 18-30 points indicate unfamiliarity. High scores indicate a high level of ethical decision-making skills.
1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Professional Values Scale for Nurses to determine the level of professional values
Time Frame: 1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).
The lowest score that can be obtained from the scale is 26 and the highest score that can be obtained is 130. High scores indicate high professional values.
1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).
Compassion Scale to determine the level of compassion
Time Frame: 1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).
The minimum score on the scale is 1 and the maximum score is 5. As the total score on the scale increases, the level of compassion also increases.
1st measurement will be made at week 1 (November 22, 2024); 2nd measurement at week 7 (January 03, 2025), 3rd follow-up measurement at week 19 (3 months later, March 31, 2025 ).

Collaborators and Investigators

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

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)

November 22, 2024

Primary Completion (Estimated)

November 22, 2024

Study Completion (Estimated)

March 31, 2025

Study Registration Dates

First Submitted

November 4, 2024

First Submitted That Met QC Criteria

November 4, 2024

First Posted (Estimated)

November 5, 2024

Study Record Updates

Last Update Posted (Estimated)

November 5, 2024

Last Update Submitted That Met QC Criteria

November 4, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

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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