The Effect of Creative Drama Education's Effects Tendencies and Emotion Management Skills

July 26, 2024 updated by: Esra Sayar, Ataturk University

The Effect of Creative Drama Education on Students' Empathic Tendencies and Emotion Management Skills

An experiential and active approach to learning can be implemented in education in higher education through all the arts. In this context, one of the artistic methods that supports active and experiential learning is creative drama. Creative drama is an educational method that is designed to achieve specified cognitive, affective and psychomotor goals and has no age or subject restrictions.This study is planned to examine the effect of the creative drama method on student midwives' empathic tendencies and their ability to manage their emotions.

Study Overview

Detailed Description

An experiential and active approach to learning can be applied to higher education through all arts. One of the artistic methods that supports active and experiential learning in this context is creative drama. Creative drama is an educational method designed to impart specific cognitive, affective, and psychomotor objectives, without age or subject limitations. The importance of creative drama lies in its ability to teach through the most realistic experience, by doing and living, thereby enhancing achievement, learning, and retention. Creative drama can be used in midwifery education to bridge the gap between theory and practice, to engage students in group activities where they can explore care practices, events, and relationships, to help students discover knowledge gaps, and to provide deeper learning. It is believed that creative drama supports midwifery students' communication skills , reflective and ethical skills, and critical thinking. Through this method, students can increase their self-awareness, develop empathy by thinking like a patient, and experience the outcomes of midwifery care. Therefore, drama can be used in midwifery education to alleviate fears and anxieties related to clinical birth experiences and to develop empathic skills.

Communication, an essential element of our lives and the foundation of information exchange, plays a significant role in the patient-midwife relationship. Establishing healthy patient-midwife communication, which requires mutual respect, support, and trust, is indispensable for the treatment process. Empathic communication plays a critical role in midwifery, a profession that dates back as far as human existence. Empathy skills, which are crucial in the development of interpersonal communication, enable people to understand the situation of others and socialize with each other.

Birth is both a universal phenomenon and a unique experience. During this process, women need the support of others. Health professionals, especially midwives and obstetricians, have significant responsibilities in providing this support . One of the primary responsibilities of the midwife is to provide emotional and physical support to the woman during labor. To provide this support effectively, midwives need to have well-developed empathy skills. Empathy is the process of accurately understanding another person's feelings and thoughts by putting oneself in their place and communicating this understanding to them.

It is known that emotions are important factors influencing human behavior. Past emotions and the anticipation of future negative events can impact an individual's present. In emotion management, it is important to focus on the present, free from the influence of the past and future.

The management of emotions becomes particularly significant in professions involving a professional identity and human relationships. The healthcare sector is an area where direct and prolonged contact with people occurs, making communication and thus emotion management crucial. Among healthcare professionals, midwives are one of the professions that interact the most with patients or their relatives.

This study aims to examine the effect of the creative drama method on the empathic tendencies and emotion management skills of student midwives.

This research was planned as an experimental type with a pre-test, post-test control group.

Place and Time the Research Was Conducted This study is an experimental study to understand the effectiveness of drama education in developing empathic tendencies and emotion management skills. The research will be conducted experimentally (pretest-posttest design in double groups). Within the 12-week/2-hour training program, drama techniques such as role playing, improvisation, pantomime, making headlines and creating photo frames will be used. The research will be conducted between March 2024 and December 2024 with students who choose the Creative Drama course at Atatürk University Faculty of Health Sciences, Department of Midwifery.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Yakutiye
      • Erzurum, Yakutiye, Turkey, 25240
        • Ataturk Universty

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:

  • No communication problems,
  • Conscious,
  • Choosing the creative drama course,
  • Individuals who volunteer to participate in the study

Exclusion Criteria:

  • Communication problems,
  • Unconscious,
  • No choosing the creative drama course,
  • Individuals who no volunteer to participate in the study

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
No Intervention: the control group
This group will consist of students who choose another elective course other than the creative drama course, and no interference will be made.
Experimental: The cretive drama group

10 weeks, once a week, each session will last approximately 2 hours and will be facilitated by a trained instructor in creative drama.

Sessions will include role-playing, improvisation, and scenario-based activities focusing on midwifery care situations, communication with patients, and empathy development.

10 weeks, once a week, each session will last approximately 2 hours and will be facilitated by a trained instructor in creative drama.

Sessions will include role-playing, improvisation, and scenario-based activities focusing on midwifery care situations, communication with patients, and empathy development.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Empathic Tendencies
Time Frame: 5-10 minutes

Empathic Tendency Scale (ETS) was developed by Dökmen (1988) to increase empathy potential in daily life. It is a Likert-type scale and consists of 20 questions and each section is given a score from 1 to 5. 3,6,7,8,11,12,13,15 while adding up the points. Questions

are collected mutually. The minimum score to be obtained from the scale is 20 and the maximum score is 100. The total score represents the subjects' empathic scores. The higher the score, the higher the empathic feature; The trait of being low indicates that the empathic trait is low. The reliability of the scale is .82.

5-10 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Emotion Management Skills
Time Frame: 5-10 minutes

It was developed by Çeçen in 2006. EMS consists of a total of 28 items, 8 of which are positive and 20 are negative. EMS is a 5-point Likert-type self-evaluation performance ranging from Not at All Suitable for Me (1) to Completely Suitable for Me (5). The highest

score that can be obtained from the scale is 140 and the lowest score is 28. While scoring the scale, reverse scores are converted in cases 1, 3, 4, 5, 6, 7, 9, 11, 13, 14, 15, 16, 18, 20, 22, 23, 24, 25, 27 and 28, which are expressed negatively. . . High scores indicate that individuals are competent in organizing their information. The scale consists of five sub- dimensions; Being able to express emotions verbally 3, 4, 7, 9, 23, 25, 27; Being able to show emotions as they are; 15, 16, 18, 20, 24,28; Ability to control the reactions of negative formations 1, 5, 11, 13; Coping 2, 17, 21, 26; Anger management includes articles 6, 22, and 14.

5-10 minutes

Collaborators and Investigators

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

Investigators

  • Study Chair: Faculty Health Science, Ataturk University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

March 30, 2024

Primary Completion (Actual)

July 11, 2024

Study Completion (Actual)

July 11, 2024

Study Registration Dates

First Submitted

July 11, 2024

First Submitted That Met QC Criteria

July 11, 2024

First Posted (Actual)

July 17, 2024

Study Record Updates

Last Update Posted (Actual)

July 29, 2024

Last Update Submitted That Met QC Criteria

July 26, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • AtaturkU-SBF-ES-00

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No, we don't plan to share individual participant data

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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