Effect of 'Empathy Dress' and Exercise on Midwifery Students' Discomfort, Empathy and Compassionate Love Levels

Sponsor
Amasya University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05731921
Collaborator
(none)
62
1
2
3.4
18

Study Details

Study Description

Brief Summary

To investigate the effect of the exercise program with the 'Empathy Dress' applied to midwifery students on the Levels of physical discomfort, empathy and compassionate love in the midwifery department of Amasya University. A total of 62 midwifery student are planned to be included in the study. Data will be collected with the "Student Information Form", "The Toronto Empathy Questionnaire- TEQ", "Evaluation Scale for Physical Discomfort", and "The Compassionate Love Scale". In the study, an exercise program that includes a total of eight sessions of 'Empathy Dress' and some exercises, every week and 20 minutes per week to the midwifery students in the experimental group, by the researcher. It is thought that the results of the study will improve the empathy and sensitive love levels of midwifery students and increase the quality of midwifery care offered.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: The exercise program with the 'Empathy Dress'
N/A

Detailed Description

Midwifery education consists of two parts, theoretical and clinical, which complement each other. Educators in the field of midwifery should strengthen students' skills before going to the clinic by following innovative training techniques. In this context, it is recommended that the simulation supported midwifery education model be used, disseminated and included in the curriculum of midwifery departments, as it contributes to students.To investigate the effect of the exercise program with the 'Empathy Dress' applied to midwifery students on the Levels of physical discomfort, empathy and compassionate love in the midwifery department of Amasya University. A total of 62 midwifery student (31 experimental, 31 control) are planned to be included in the study. Data will be collected with the "Student Information Form", "The Toronto Empathy Questionnaire- TEQ", "Evaluation Scale for Physical Discomfort", and "The Compassionate Love Scale". In the study, an exercise program that includes a total of eight sessions (two months) of 'Empathy Dress' and some exercises (stairs going up and down, sitting up, putting on trousers, tying shoes, etc.), every week and 20 minutes per week to the midwifery students in the experimental group, by the researcher. The expected result of the study is to determine whether the exercise program with the 'Empathy Dress' is an effective intervention in increasing the empathy and compassionate love levels in midwifery students. In addition, the effect of the 'Empathy Dress' and exercise program on the physical discomfort levels of midwifery students is investigated. It is thought that the results of the study will improve the empathy and sensitive love levels of midwifery students and increase the quality of midwifery care offered.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
62 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A randomized controlled trial with pretest-posttest control groupA randomized controlled trial with pretest-posttest control group
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Investigation of the Effect of the Exercise Program With the 'Empathy Dress' Applied to Midwifery Students on the Levels of Physical Discomfort, Empathy and Compassionate Love: A Randomized Controlled Study
Anticipated Study Start Date :
Feb 15, 2023
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

The exercise program with the 'Empathy Dress'

Behavioral: The exercise program with the 'Empathy Dress'
The experimental group will be given an exercise program that includes a total of eight sessions (two months) of 'Empathy Dress' and some exercises (stairs going up and down, sitting up, putting on trousers, tying shoes, etc.), every week and 20 minutes per week, by the researchers.

No Intervention: Control group

No intervention

Outcome Measures

Primary Outcome Measures

  1. Empathy Level [2 months]

    Empathy is one of the primary outcomes. This will be measured using 'The Toronto Empathy Questionnaire- TEQ'. The minimum score that can be obtained from the scale is "13", the maximum score is "65", and as the score obtained from the scale increases, empathy levels also increase.

  2. Compassionate Love Level [2 months]

    Compassionate Love Level is the other primary outcomes. This will be measured using 'The Compassionate Love Scale'. The minimum score that can be obtained from the scale is "21", the maximum score is "147", and as the score obtained from the scale increases, Compassionate Love levels also increase.

Secondary Outcome Measures

  1. Physical Discomfort Level [2 months]

    Physical Discomfort Level is the other primary outcomes. This will be measured using 'Evaluation Scale for Physical Discomfort'. This form was developed by the researchers and consists of 4 items. The score ranges from 0 to 10 points, with increasing score reflecting more discomfort.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Volunteering to participate in the study

  • Absence of a defined psychiatric disorder

  • There is no problem that prevents communication

Exclusion Criteria:
  • Those who have movement system problems that prevent them from exercising with increasing weights by adapting to their pregnancy weeks,

  • Individuals who do not meet the inclusion criteria or who do not volunteer to participate in the research despite meeting them will be excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Amasya University Amasya Turkey 05000

Sponsors and Collaborators

  • Amasya University

Investigators

  • Principal Investigator: Emine İbici Akça, Ph.D, Amasya University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emine Akca, Assist. Prof. Dr. in the Amasya University Midwifery Department, Amasya University
ClinicalTrials.gov Identifier:
NCT05731921
Other Study ID Numbers:
  • Amasya Univ
First Posted:
Feb 16, 2023
Last Update Posted:
Feb 16, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Emine Akca, Assist. Prof. Dr. in the Amasya University Midwifery Department, Amasya University

Study Results

No Results Posted as of Feb 16, 2023