- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05166941
THE EFFECT OF CREATIVE DRAMA ON THE DEVELOPMENT OF ANXIETY, EMPATHY AND COMMUNICATION SKILLS IN NURSING EDUCATION
December 12, 2021 updated by: Günseli Uzunhasanoğlu, Ankara Yildirim Beyazıt University
In Psychiatric Nursing Education; The Effect of Creative Drama Method Based on Travelbee's "Human to Human Relationship" Theory on Developing Anxiety, Empathy and Communication Skills
This work; The aim of this study is to determine the effect of the education program, which was created with the creative drama method based on Travelbee's "human-to-human relationship" theory, on the teaching and practice of mental health and psychiatric nursing course, on reducing the anxiety of students and improving their empathy and communication skills.
Study Overview
Detailed Description
In psychiatric nursing education; It is known that classical education methods are not sufficient to reduce students' anxiety and stigma, and to strengthen communication and empathy.
For this reason, there is a need for training methods that will increase in-depth learning and communication skills and empathy in the field.
In this research, the creative drama education method was arranged in accordance with the requirements of mental health and psychiatric nursing education and a training program was developed.
Within the scope of the research, this training program was applied to the students who completed the theoretical education of psychiatric nursing.
In order to measure the effectiveness of the research training program, it was planned in a quantitative design as a randomized controlled intervention study and in a mixed method in qualitative design in order to examine students' views on the method.
Study Type
Interventional
Enrollment (Actual)
26
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
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-
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Ankara, Turkey, 06100
- Ankara Yildirim Beyazit University
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-
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
21 years to 24 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being residing in the city center of Ankara Volunteering to participate in the research, Being a 4th year nursing student and having completed the Mental Health and Diseases Nursing course, Lack of clinical experience in communicating with individuals with mental illness (Health Vocational High School graduate), Not having received training in communicating with individuals with mental illness before (students repeating a grade).
Not having been diagnosed with any mental illness No mental illness in first degree relatives
Exclusion Criteria:
- Living outside the city center of Ankara To fill in the research data collection forms incompletely, Not completing the creative drama education based on human-human relationship theory, Refusal to participate in the research Not meeting the criteria for inclusion in the research
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
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
It is a closed group in which the training program is implemented.
|
In the training program, a total of six games were played about the experiences of psychiatric patients.
The program was designed to be two game per week for four weeks.
|
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No Intervention: Control Group
No training program was applied to this group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Numerical Rating Scale(NRS)
Time Frame: Eight weeks
|
It was applied to the experimental and control groups to quantitatively measure the effectiveness of the training program.
|
Eight weeks
|
|
Qualitative method, (focus group interview)
Time Frame: one weeks
|
It was applied to evaluate the opinions and suggestions of the experimental group about the education program.
|
one weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Empathic Skill Scale - B
Time Frame: Eight weeks
|
It was used to determine the level of empathic skills of the students at the end of the training program.
|
Eight weeks
|
|
Communication Skills Assessment Scale
Time Frame: Eight weeks
|
It was used to determine the level of communication skills of the students at the end of the education program.
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Eight weeks
|
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State and Trait Anxiety Scale
Time Frame: Eight weeks
|
It was used to determine the level of anxiety experienced by the students at the end of the education program.
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Eight weeks
|
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semi-structured questionnaire
Time Frame: one weeks
|
It was applied to evaluate the opinions and suggestions of the experimental group about the education program
|
one weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: günseli uzunhasanoğlu, Phd, Ankara Yildirim Beyazıt University
- Study Director: Birgul Ozkan, Phd, Ankara Yildirim Beyazıt University
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)
May 27, 2021
Primary Completion (Actual)
July 20, 2021
Study Completion (Actual)
October 20, 2021
Study Registration Dates
First Submitted
December 12, 2021
First Submitted That Met QC Criteria
December 12, 2021
First Posted (Actual)
December 22, 2021
Study Record Updates
Last Update Posted (Actual)
December 22, 2021
Last Update Submitted That Met QC Criteria
December 12, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ankara YBU-SBF-GU-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
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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