- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06760780
Osteoporosis Awareness Among Nursing Students
Effect of Scenario-based Teaching on Osteoporosis Awareness in Nursing Students: a Randomized Controlled Trial
The aim of this clinical study is to determine the effect of scenario-based training of nursing students on awareness of osteoporosis.
To this end, the most important questions to be answered in the study are
- What is the level of osteoporosis awareness among nursing students at the start of the study?
- Does scenario-based education have an impact on osteoporosis awareness?
Participants:
All student nurses participating in the study will first receive theoretical training on osteoporosis. At the end of the training, a scenario example prepared by the researchers on the topic of osteoporosis is worked on with the students in the experimental group. No additional intervention is carried out with the control group.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Esra Çavuşoğlu, Doctorate
- Phone Number: 14237 +90324 361 00 01
- Email: esracavusoglu@mersin.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18 years of age and above,
- Mersin University Faculty of Nursing 2nd year students,
- Have not received any other training on osteoporosis before,
- Willing to participate in the research,
- Have cognitive competence to fill out the data collection form,
- Those who sign the Informed Voluntary Consent Form will be included.
Exclusion Criteria:
- Those under the age of 18,
- Not a 2nd year student at Mersin University Faculty of Nursing,
- Have previously received different training on osteoporosis,
- Do not want to participate in the research,
- Do not have the cognitive ability to fill out the data collection form,
- Those who do not sign the Informed Consent Form will not be included.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group: Scenario group
Theoretical lesson on osteoporosis and a scenario example on osteoporosis will be covered with the experimental group.
|
The experimental group will first be given a theoretical lesson prepared in line with the current literature on osteoporosis.
At the end of the lesson, a prepared scenario example on osteoporosis will be covered.
|
|
Other: Other: Control group
The control group will be given a theoretical lesson on osteoporosis.
No additional intervention will be made.
|
The control group will only be given a theoretical lesson prepared in line with the current literature on osteoporosis.
No other intervention will be made.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Osteoporosis awareness level will be assessed using the Osteoporosis Awareness Scale.
Time Frame: Change from before implementation and 4th week of practice
|
The Osteoporosis Awareness Scale consists of 31 items and 5 subscales.
Responses to scale items are rated on a 4-point Likert-type scale ranging from 1 to 4 (4 = I know very well, 3 = I know, 2 = I know a little, 1 = I don't know at all).
The lowest and highest possible scores from the scale are 31 and 124, respectively.
The higher the average score obtained from the overall scale, the higher the osteoporosis awareness.
|
Change from before implementation and 4th week of practice
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Esra Çavuşoğlu, Doctorate, Mersin University
- Principal Investigator: Meral Gün, Doctorate, Mersin University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- MersinUni.
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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