- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06653335
Effectiveness of the Education Support Program Provided Via Text Message
October 19, 2024 updated by: Marmara University
EFFECTIVENESS of the EDUCATION SUPPORT PROGRAM VIA TEXT MESSAGE
Information will be provided to first year midwifery students via text message within the scope of the 'Basic Principles and Practice in Midwifery Education' support programme.
This information is planned to last approximately 4 weeks.
The study will be conducted to evaluate the effect of the information provided on the knowledge levels of the students.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
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 Contact
- Name: Serkan Çalışmaz Secretary, Bachelor' s Degree
- Phone Number: +905317340258
- Email: sserkancalismaz@gmail.com
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:
- In 2023-2024 Spring Term, with the success of the Basic Principles and Practices Course in Midwifery to have completed the programme,
- Having a mobile phone,
- Accepting to participate in the research is one of the inclusion criteria of this studyc
Exclusion Criteria:
- Students who incompletely completed the post-test and first test scales will be excluded from 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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
All students to be included in the study will be pre-tested through Google Form's.
After the pre-test, the students in the experimental group will be sent images created by the researchers via text message for 4 weeks (22 days) and consisting of the information given in the Basic Principles and Practices in Midwifery Course.
Each visual will contain one piece of information.
The researchers will send 6 visuals to the students in the experimental group via text message every day for 4 weeks, except Saturdays and Sundays.
The post-test will be applied immediately after the end of the implementation process.
The messages will be short and contain a single piece of information.
|
All students to be included in the study will be pre-tested via Google Form's.
After the pre-test, the students in the experimental group will be sent images created by the researchers via text message for 4 weeks (22 days) and consisting of the information given in the Basic Principles and Practices in Midwifery Course.
Each visual will contain one piece of information.
The researchers will send 6 visuals to the students in the experimental group via text message every day for 4 weeks, except Saturdays and Sundays.
The post-test will be applied immediately after the end of the implementation process.
The messages will be short and contain a single piece of information.
|
|
No Intervention: Control Group
No treatment will be carried out.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge Measurement Questionnaire
Time Frame: Before and immediately after education
|
The knowledge measurement questionnaire prepared by the researchers according to the curriculum of the related course consists of 133 questions in total.
There are 'Yes' or 'No' choices in the questions.
Out of 33 questions, those who give the correct answer will be scored as 1 and those who give the wrong answer will be scored as 0. The knowledge measurement questionnaire will be applied in pre-test and post-test.
The pre-test will be applied just before the start of the study and the post-test will be applied just after the end of the implementation process.
|
Before and immediately after education
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
General Publications
- Huang, C. S. J., Yang, S. J. H., Chiang, T. H. C., & Su, A. Y. S. (2016). Effects of Situated Mobile Learning Approach on Learning Motivation and Performance of EFL Students. Educational Technology & Society, (2016), 19 (1), 263-276.)
- Hardini, M. G., Khaizure, T., & Godwin, G. (2024). Exploring the Effectiveness of E-Learning in Fostering Innovation and Creative Entrepreneurship in Higher Education. Startupreneur Business Digital (SABDA Journal), 3(1), 34-42. https://doi.org/10.33050/sabda.v3i1.441
- Kavruk Y. (2018). Uzaktan Öğrenenlerin Kısa Mesaj ile Eğitsel Destek Sağlanmasına Yönelik Memnuniyetleri ve Öğrenme Düzeyleri. Anadolu Üniversitesi Sosyal Bilimler Enstitüsü, Yüksek Lisans Tezi. Eskişehir. 2018.
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 30, 2024
Primary Completion (Estimated)
December 30, 2024
Study Completion (Estimated)
December 30, 2024
Study Registration Dates
First Submitted
October 19, 2024
First Submitted That Met QC Criteria
October 19, 2024
First Posted (Actual)
October 22, 2024
Study Record Updates
Last Update Posted (Actual)
October 22, 2024
Last Update Submitted That Met QC Criteria
October 19, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- MarmaraUEBE2
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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