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Scape Room With High Fidelity Simulators

Sponsor
University of Extremadura (Other)
Overall Status
Completed
CT.gov ID
NCT05122871
Collaborator
(none)
40
Enrollment
1
Location
2
Arms
10
Actual Duration (Months)
4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The objective of the present study is assess the efficcacy in the acquisition of knowledge and practical skills of a scape room with high definition simulators.

An experimental trial will be carried out in which the students of the intervention group will receive practical training on newborn care in the delivery room through the development of a scape room with high-fidelity simulators. The control group students will receive practical training only with the use of high-fidelity simulators. The participants of both groups will previously receive a theoretical training of 10 hours. Knowledge acquisition and student satisfaction with both methodologies will be analyzed.

Condition or Disease Intervention/Treatment Phase
  • Other: Scape Room
  • Other: Simulation
 N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
Scape Room With High Fidelity Simulator: Results in the Learning and Satisfaction of Nursing Degree Students
Actual Study Start Date :
Mar 1, 2021
Actual Primary Completion Date :
Jul 31, 2021
Actual Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Scape room

Other: Scape Room
Practical training through scape-room with simulator
Active Comparator: Simulation

Other: Simulation
Practical training through simulator

Outcome Measures

Primary Outcome Measures

  1. Knowledge test [1 month after training session]

    The degree of knowledge and skills related to the care of the newborn will be measured by means of an evaluation questionnaire that will consist of 20 multiple choice questions..

Secondary Outcome Measures

  1. Satisfaction likert scale [1 month after training session]

    the degree of student satisfaction with the methodology used will be evaluated with a 6-item likert scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Nursing degree students of University of Extremadura
Exclusion Criteria:

  • 1st year nursing degree students

  • Nursing degree students of other universities

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cristina Franco Antonio Cáceres Spain 10003

Sponsors and Collaborators

  • University of Extremadura

Investigators

  • Principal Investigator: Cristina Franco Antonio, PhD, University of Extremadura

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cristina Franco Antonio, Associate Professor of nursing studies, University of Extremadura
ClinicalTrials.gov Identifier:
NCT05122871
Other Study ID Numbers:
  • 16/2021
First Posted:
Nov 17, 2021
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 17, 2022