- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06046378
The Effect of Digital Stories Prepared With Digital Audio File (Podcast) on Midwifery Learning
The Effect of Digital Stories Prepared With Digital Audio File (Podcast) on Midwifery Learning: A Randomized Controlled Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Primary aim: The study is to determine the effect of digital stories prepared with digital audio files (podcasts) on learning in midwifery education.
Hypotheses:
H0: There is no difference between the knowledge test mean scores of the students in the experimental and control groups.
H1: There is a statistically significant difference between the knowledge test mean scores of the experimental and control group students.
H2: There is a statistically significant difference between the satisfaction of the experimental and control group students.
H3: There is no statistically significant difference between the satisfaction of the experimental and control group students.
This study was designed as a randomized controlled experimental study. The study will be carried out at Kocaeli University Faculty of Health Sciences between October 2022-November 2022.
In order to facilitate data collection, the universe of the research will be composed of 70 3rd year midwifery students of Kocaeli University Faculty of Health Sciences in the 2022-2023 academic year. The sample size was based on a study previously published in the literature in 2013 to evaluate the training given to midwifery students on the legal and religious aspects of egg donation through a digital audio file (podcast). The sample calculation was calculated with the G*Power 3.1.9.2 program according to the data of the relevant article.With the obtained values, the effect size was calculated as 0.974. G*Power 3.1.9.2 program effect size and minimum number of students to be included in the study sample: 0.974; a=0.05; power was calculated as 0.95 and the sample size was determined to be less than 16. In order to increase the power of the analysis, the number of samples has been increased and n=16 midwifery students will be included in each group. The experimental group n=16 and the control group n=16) were designed as a digital story prepared in the form of a digital audio file (podcast). In which group the students included in the study will be will be determined from the "Research Lists" website of the random number generation program and will be divided into two groups.
Randomization: The group of mothers will be determined from the random number generator site called "Random Lists". Students will be divided into two groups as experimental and control groups. Thus, the number of each student will be determined and recorded.
Research data were collected by using the Participant Information Form, Knowledge Test and the Questionnaire for Evaluating the Efficiency of Digital Stories Prepared as a Digital Audio File (Podcast).
Exhibitor Information Form: The participant information form was created as a result of the literature review. With this form, students' age, employment status, education status of their parents, the place where they stay during the student period, the place where they provide internet access, the duration and purposes of internet use, the reasons for choosing the midwifery department, the internet usage status in midwifery education and the digital audio file (podcast) before. It includes the situation of listening to the digital story prepared in the form of a digital story and his thoughts on the use of digital stories prepared in the form of a digital audio file (podcast) in midwifery education.
Knowledge test: It was prepared as 50 questions in order to measure the learning levels of the students, the information conveyed by digital stories prepared in the form of digital audio files (podcast). For the knowledge test created, arrangements were made by 10 expert midwife academicians by taking expert opinions. The relevant knowledge test was applied as a pre-test in the first encounter with the students. After listening to the digital stories prepared with a digital audio file (podcast), the experimental group was administered as a post-test and three weeks later as a permanence test.
Digital Stories Prepared with a Digital Audio File (Podcast): The stories created by the researchers as a result of the literature review consisted of three parts: preparation for natural birth, ideal birth environment and storytelling of a natural birth. In the first part, Eda and Melisa's Birth Journey, in the second part, Eda and Melisa's Birth Circle, and in the third part, Eda and Melisa's Meeting Moment. These stories were turned into digital audio files (podcasts) by an educator from Kocaeli University Faculty of Communication who are experts in digital audio files (podcast) designs, in an appropriate environment and quality, and transmitted to the students.
Questionnaire for Evaluating the Efficiency of Digital Stories Prepared with a Digital Audio File (Podcast): It is a form consisting of seven questions and 28 statements and was used to evaluate the effectiveness of digital stories to the experimental group students.
Before the research, a pilot study will be conducted with the 3rd year students of the Department of Midwifery, Faculty of Health Sciences, Selcuk University. This pilot study will be carried out between 26.09.2022 and 30.09.2022 by the researcher using face-to-face interview technique. Students will be asked not to share the study with other students and on social media platforms by signing a consent form and confidentiality agreement.
The main study will be carried out with Kocaeli University Midwifery 3rd year students. Between October 3 and October 7, 2022, which is the beginning of Kocaeli University 2022-2023 academic year academic calendar, a meeting will be held with students about extracurricular work and details will be shared. Participants will be informed that they can leave the research at any time and the study will be completed with volunteer participants. All students participating in the study will sign a confidentiality agreement and it will be ensured that they do not share their work with other students and on platforms such as social media. A participant information form consisting of 22 questions and a knowledge test consisting of 50 statements (pre/post test for natural birth and permanence test) will be applied to both groups.
Randomization will be made among the students who accepted to participate in the study, and two groups will be formed as experimental and control groups. Digital stories prepared with a digital audio file (podcast) will be sent to the students in the experimental group via e-mail. At the end of the relevant topic at the time planned in the academic calendar, a face-to-face interview will be provided to both groups, and a post-test will be applied to both groups. A questionnaire for evaluating the effectiveness of digital stories prepared with a digital audio file (podcast) will be applied to the experimental group students. All students will be given a retention test 21 days after the post-test. After the permanence test is applied, digital stories will be sent to the students in the control group via e-mail.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Kocaeli, Turkey, 41380
- Kocaeli University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- In the 18-30 age range,
- Kocaeli University Faculty of Health Sciences, 3rd year midwifery student,
- Not absenteeism,
- Volunteer to participate in the study and complete the relevant forms,
- No auditory problem,
- Students who have listened to digital audio files (podcasts) at least once
- Able to speak and understand Turkish,
- The mothers who agreed to participate in the study
Exclusion Criteria:
- Those who want to leave the study for any reason during the research process,
- Does not have a mobile phone,
- Have received training on normal birth before,
- Not completing the questionnaires,
- Students who do not listen to digital audio files (podcasts)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Digital Story Group Prepared With Digital Audio File (Podcast)
The students determined as a result of the randomization will be given a pre-test before the introduction to the "Normal Birth and Postpartum Period " course, which is planned according to the academic calendar.
Simultaneously with the subject, digital stories prepared with a digital audio file (podcast) will be sent to the students via e-mail and they will be listened to.
|
The students determined as a result of the randomization will be given a pre-test before the introduction to the "Normal Birth and Postpartum Period " course, which is planned according to the academic calendar.
Simultaneously with the subject, digital stories prepared with a digital audio file (podcast) will be sent to the students via e-mail and they will be listened to.
At the end of the subject on the date planned according to the academic calendar, the students will be interviewed again and a questionnaire will be applied to evaluate the effectiveness of the digital stories prepared with the post-test and digital audio file (podcast).
The retention test will be applied 21 days after the last test application.
|
|
Active Comparator: Control
The students in the control group will listen to the Normal Birth and Postpartum term course face-to-face with the classical education approach.
The knowledge level of the students will be measured with the knowledge tests.
|
After the students in the control group are determined, a pre-test will be conducted before the subject receives education.
The same knowledge test will be repeated as a post-test after the students receive the classical course education and after the end of the subject.
Students will be given a retention test 21 days after the last test.
After the retention test application, digital stories prepared with a digital audio file (podcast) will be sent to the students in the control group.
In this way, all students participating in the study will have access to the training material used in addition.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Natural birth and non-pharmacological methods information sheet
Time Frame: 1 day (form filled in 30 minutes)
|
It will be applied as a pre-test to determine the knowledge level of the students.The knowledge levels of the students about natural birth and non-pharmacological methods were measured.
It was prepared as 50 questions by the researchers, each question was evaluated over two points and an evaluation was made out of 100 points.
The lowest score of the test is 0, and the highest score is 100.
As the score obtained from the test increases, it means that the knowledge level of the students increases.
It was administered to all students as a pre-test.
Before the Natural Birth and Non-Pharmacological Methods were explained to the students in the Normal Birth and Postpartum Period course.
|
1 day (form filled in 30 minutes)
|
|
Natural birth and non-pharmacological methods information sheet
Time Frame: The students in both groups were interviewed it was applied as a post-test 3 weeks after the pre-test (form filled in 30 minutes)
|
It will be applied as a post-test to determine the knowledge level of the students.The knowledge levels of the students about natural birth and non-pharmacological methods were measured.
It was prepared as 50 questions by the researchers, each question was evaluated over two points and an evaluation was made out of 100 points.
The lowest score of the test is 0, and the highest score is 100.
As the score obtained from the test increases, it means that the knowledge level of the students increases.
It was administered to all students as a pre-test.
Before the Natural Birth and Non-Pharmacological Methods were explained to the students in the Normal Birth and Postpartum Period course.
|
The students in both groups were interviewed it was applied as a post-test 3 weeks after the pre-test (form filled in 30 minutes)
|
|
Natural birth and non-pharmacological methods information sheet
Time Frame: The same knowledge test was applied to all students as a retention test 3 weeks after the students took the post-test (Students were given 30 minutes to solve the test)
|
The knowledge levels of the students about natural birth and non-drug methods were measured.
It was prepared as 50 questions by the researchers, each question was evaluated over two points and an evaluation was made out of 100 points.
The lowest score of the test is 0, and the highest score is 100.
As the score obtained from the test increases, the knowledge level of the students also increases.
|
The same knowledge test was applied to all students as a retention test 3 weeks after the students took the post-test (Students were given 30 minutes to solve the test)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayla Ergin, Proff. Dr., Kocaeli University
- Study Chair: Ebru Aktaş, Kocaeli University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ayla-1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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