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Not yet recruiting NCT07692568

VIDEO LEARNING FOR EMPATHY, ETHICS AND FAMILY WITNESSED RESUSCITATION

No phase Interventional Family Witnessed Resuscitation Empathy Education Ethics Nursing Education Nursing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 360 Degree Virtual Reality Video, 2D Standard Video.
Who it may be relevant to
Registry conditions: Family Witnessed Resuscitation, Empathy Education, Ethics Nursing, Education Nursing. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

THE EFFECT OF A VIDEO BASED DIGITAL LEARNING INTERVENTION ON NURSING STUDENTS PERCEPTIONS OF EMPATHY, ETHICAL SENSITIVITY, AND FAMILY WITNESSED RESUSCITATION IN THEIR PATIENT PERSPECTIVE EXPERIENCES: A RANDOMIZED CONTROLLED TRIAL

Overview

This clinical trial (randomized controlled experimental study) aims to learn about the effects of presenting the family-witnessed CPR process from a patient's perspective through 360° virtual reality and 2D video within second-year nursing students. The primary question(s) / hypotheses it aims to answer are: * H1: Will the content validity ratio of the developed scenario be above 0.80? * H2: Is the increase in empathy scores (pre-test/post-test difference) of students in the 360° VR group significantly higher compared to the 2D video and control groups? * H3: Is the increase in ethical sensitivity scores of students in the 360° VR group significantly higher compared to the 2D video and control groups? * H4: Is the change in perception scores toward family-witnessed CPR more positive in the 360° VR group compared to the other groups, and is their mean SUS (System Usability Scale) score at or above the acceptability threshold of 70? * H5: Is the VES (Video Engagement Skale) score of students in the 360° VR group significantly higher than that of the 2D video group? Researchers will compare the 360° immersive video (360° VR) group, the 2-dimensional (2D) video group, and the control group to see if there are effects on empathy, ethical sensitivity, perception of risks-benefits of family presence, self-confidence regarding family presence, video engagement, and system usability. Participants will be asked to: * Watch the scenario reenactment involving a family-witnessed CPR process, recorded via a 360° camera (in either 360° VR or 2D format, depending on their assigned group). * Complete data collection tools consisting of the Introductory Information Form, "Jefferson Scale of Empathy", "Ethical Sensitivity Questionnaire", "Family Presence Risk-Benefit Scale and Family Presence Self-Confidence Scale", "System Usability Scale (SUS-TR)", and "Video Engagement Skale(VES)".

Interventions

  • Behavioral 360 Degree Virtual Reality Video
    Immersive 360-degree virtual reality video scenario of family-witnessed cardiopulmonary resuscitation presented from a patient perspective.
  • Behavioral 2D Standard Video
    Standard 2-dimensional video scenario of family-witnessed cardiopulmonary resuscitation presented from a patient perspective.

Primary outcome measures

  • Change in Jefferson Scale of Empathy Scores [Time frame: Baseline (Pre-test) and right after the intervention (Post-test)]
  • Change in Ethical Sensitivity Questionnaire Scores [Time frame: Baseline (Pre-test) and right after the intervention (Post-test)]
  • Change in Family Presence Risk Benefit Scale and Family Presence Self Confidence Scale Scores [Time frame: Baseline (Pre-test) and right after the intervention (Post-test)]
  • System Usability Scale Scores [Time frame: Right after the intervention (Post-test)]
  • Video Engagement Scale Scores [Time frame: Right after the intervention (Post-test)]

Eligibility criteria

Inclusion criteria

  • Being a second-year undergraduate nursing student
  • Volunteering to participate in the study and signing the informed consent form
  • Not having participated in a similar virtual reality or family-witnessed CPR study before

Exclusion criteria

  • Having a diagnosed neurological or psychiatric disorder that prevents using virtual reality glasses (such as epilepsy, severe vertigo, or motion sickness)
  • Having uncorrected visual or hearing impairments
  • Not completing all stages of the study (pre-test, intervention, or post-test)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Turkey (Türkiye) · 1 center
  • Sakarya University — Sakarya

Identifiers

NCT: NCT07692568 · E-61923333-050.99-597961

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗