Skip to content

The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning

The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning:a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04136691
Enrollment
61
Registered
2019-10-23
Start date
2018-02-19
Completion date
2018-04-12
Last updated
2019-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burns, Patient Simulation

Keywords

Simulation, Nursing education, Burns, Nursing process

Brief summary

Aim: This research was conducted as a single-blind randomized control group intervention trial to determine the effectiveness of simulation method performed using high-fidelity human patient simulator in nursing students' burn patient care planning.

Detailed description

Materials and Methods: The research was carried out with randomly-selected 61 students including 31 in intervention and 30 in control groups who took the Surgical Diseases Nursing Course in the spring term of the 2017-2018 academic year. The research data were collected using Personal Information Form, Cognitive Level Assessment Test for Burn Patient Care, The Student Satisfaction and Self-Confidence in Learning Scale, Simulation Design Scale, Educational Practices Questionnaire, and Evaluation Form for Burn Patient Care Plan. In the application process of the research, knowledge tests were administered as a pretest, second test, and posttest, and first and second applications of burn patient care plans were performed with all students. In the research, the application of burn patient scenario was performed only with the intervention group. Descriptive statistics, Chi-Square, Mann-Whitney U Test, and Wilcoxon Sign Test were used to analyze the data.

Interventions

OTHERsimulation training

Burn patient scenario was performed with the intervention group.

Sponsors

Çankırı Karatekin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Investigator)

Masking description

Single blind

Eligibility

Sex/Gender
ALL
Age
19 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

* Enrolled in the course * Had not taken this course and any training on burn patient care before * Accepted to participate in the research

Exclusion criteria

* Have any records of absence * Taken this course and training on burn patient care before * Graduate of health vocational high school

Design outcomes

Primary

MeasureTime frameDescription
Differences of knowledge scores between groupsThe first knowledge test was conducted in the first week, the second knowledge test in the fourth week (1 week after simulation application) and the third knowledge test in the fifth week. Total duration 5 weeks.First, second and third knowledge tests were applied to measure the level of knowledge.

Secondary

MeasureTime frameDescription
Differences of nursing interventions scores between groupsThe first burn patient care plan was implemented in the second week and the second care plan in the fifth week (2 weeks after simulation application).The first and second burn patient care plans were applied to measure the level of care planning.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026