None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants who meet the eligibility criteria, understand the purpose of the study, and voluntarily provide written informed consent will be enrolled. After recruitment, participants will be randomly assigned to either the experimental group or the control group in a 1:1 ratio using a computer-generated randomization sequence. The inclusion criteria are as follows: ? Third-year undergraduate nursing students. ? Nursing students with clinical practice experience. ? Nursing students who have not completed a course on nurses' legal responsibilities. ? Nursing students who understand the purpose of the study and voluntarily provide informed consent to participate.
Exclusion criteria
Exclusion criteria: ? Nursing students who have completed a formal course on nurses' legal responsibilities, medical law, patient information protection, or nursing documentation. ? Nursing students who are unable to participate in all educational sessions or complete all questionnaires during the study period. ? Nursing students who decline to provide informed consent or withdraw from the study at any time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients’ Health Information Protection Awareness | — |
Secondary
| Measure | Time frame |
|---|---|
| Nursing Documentation Knowledge;Intention to Practice Patient Information Protection | — |
Countries
Korea, Republic of
Contacts
Chung-Ang University