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The Impact of Experiential Simulation on Nursing Students

NCT07763444 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2026-08-13

No results posted yet for this study

Summary

Patients with impaired renal functions sustain their lives through kidney transplantation or various dialysis methods. Peritoneal dialysis, one of these methods, is based on the administration of 1.5-3 liters of dialysis solution into the patient's peritoneal cavity and the replacement of this solution at 4-6 hour intervals. The continuous presence of this solution in the peritoneum creates a significant physical burden for the patient. It is crucial for nurses to be aware of this physical load and the challenges patients face throughout the process, to understand them, and to develop empathy. A nurse's understanding of the patient facilitates treatment adherence, improves quality of life, and supports the patient's motivation.

In this study, a weight-based simulation will be implemented to enhance nursing students' empathy levels and caring behaviors. Students will be equipped with a 2 kg weight for four-hour periods to experience the physical burden endured by peritoneal dialysis patients. Following the intervention, students' empathy levels, caring behaviors, and perspectives regarding the experience will be evaluated. It is anticipated that the findings of this study will provide valuable insights into the empathy levels and caring behaviors of nursing students. Furthermore, the students' feedback is expected to guide nursing education, academics, and clinical nurses in providing care for patients undergoing peritoneal dialysis.

Conditions

  • Nursing Students

Interventions

OTHER

Application of weights

Weights will be attached to the waist of the participants in the experimental group

Sponsors & Collaborators

  • Necmettin Erbakan University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-05-01
Primary Completion
2026-05-30
Completion
2026-05-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07763444 on ClinicalTrials.gov