- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05424770
The Effect of the Crossword Used in Nursing Education on Learning Success
August 7, 2023 updated by: Sevgi Deniz Dogan, Cukurova University
The Effect of Crossword Used as an Active Learning Tool in Nursing Education on Learning Achievement: A Randomized Controlled Study
The research was planned as a randomized controlled study to evaluate the effect of crossword, which are an active learning tool, on the success of learning information about pain control in nursing education.
Research data is planned to be collected in Hatay Mustafa Kemal University Faculty of Health Sciences.
The universe of the research will be the students who take the 3-credit pain control course in the aforementioned faculty in the fall semester.
The sample of the research will consist of 72 students who meet the inclusion criteria and agree to participate in the research verbally and in writing.
The data of the research will be collected by using the Personal information form prepared in line with the literature, and Success Tests (3 tests) prepared separately for each stage.
SPSS program will be used in the analysis of the data.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
72
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
-
-
-
Hatay, Turkey
- Hatay Mustafa Kemal University Institute of Health Sciences
-
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- To be registered in the pain course,
- Taking the pain course for the first time,
- Absence of any psychiatric disorder that will reduce the ability to comprehend and understand,
- Agreeing to participate in the research.
Exclusion Criteria:
-Willingness to leave 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: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experiment group
During the 3 weeks in which the subjects related to pain control are explained, the standard lecture (explanation with ppt presentation) will be made as in the normal course of the course.
Afterwards, puzzle activities prepared by the researcher will be implemented and students will be actively involved in the process.
|
Afterwards, crossword activities prepared by the researcher will be implemented and students will be actively involved in the process.
The researcher will also include a collaborative learning environment where students can exchange information with each other.
After the completion of each puzzle, the researcher will make the necessary checks and corrections.
|
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No Intervention: control group
During the 3 weeks in which the subjects related to pain control are explained, the standard lecture (explanation with ppt presentation) will be made as in the normal course of the course.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The effect of crossword on learning achievement in nursing education
Time Frame: Three months
|
Evaluation will be made with a multiple-choice (5-choice) achievement test, which will be prepared by the researchers within the scope of the application.
This test will consist of 20 items.
After the test is prepared, item analysis will be made and it will be presented to the expert opinion.
In the test, each correct answer will be scored as 1 and each incorrect answer as 0. The higher the score, the higher the success will be interpreted.
|
Three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 15, 2022
Primary Completion (Actual)
November 30, 2022
Study Completion (Actual)
December 31, 2022
Study Registration Dates
First Submitted
June 15, 2022
First Submitted That Met QC Criteria
June 15, 2022
First Posted (Actual)
June 21, 2022
Study Record Updates
Last Update Posted (Actual)
August 8, 2023
Last Update Submitted That Met QC Criteria
August 7, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 5312256942
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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