- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06225401
Technical Skills Training in Undergraduate Nursing Students: SimCapture for Skills. (Simcapture)
Study to Evaluate the Cost-effectiveness of SimCapture for Skills Digital Technology for the Acquisition of Technical Skills Competencies in Peer-to-peer Learning of Undergraduate Nursing Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The traditional teaching with a teacher in the classroom will be received by all the students enrolled in the course. Among these students, two intervention groups will be assigned. One group will train the skills practice with the SimCapture for Skills interface before the traditional teaching with the teacher in the classroom (PRE group) and another group will do it afterwards (POST group).
Skills training:
Prebriefing phase: the court of students, before attending the practice with the low fidelity simulator, both in traditional teaching and teaching with SimCapture, will study in the Virtual Campus of the subject, the procedure of how to perform the technique (sequence of actions) in Word format, and will visualize an example video. They will be administered a knowledge test before the practice to evaluate the acquisition of theoretical concepts.
Simulation phase:
In traditional teaching (2h duration) students will practice in pairs, with the low fidelity simulator, the blood collection technique. The teacher will give them immediate feedback as they practice the technique (zone 0 of the SimZones model). The ratio is 1 teacher to 8 students.
In the PRE intervention group (before the traditional teaching) students will practice in pairs, with the same low fidelity simulator, the blood collection technique without a teacher in the classroom. In the SimCapture for Skills interface, the procedure of how to perform the technique (sequence of actions) will be developed in checklist format for the student to check step by step. They will be provided with the same material and classroom time as in traditional teaching (2h). In each classroom there will be 8 students (4 pairs) and one teacher will supervise 2 classrooms.
In the POST intervention group (after the traditional teaching) the students will practice in pairs, with the same low fidelity simulator, the blood collection technique without a teacher in the classroom. In the SimCapture for Skills interface, the procedure of how to perform the technique (sequence of actions) will be developed in checklist format for the student to check step by step. They will be provided with the same material and classroom time as in traditional teaching (2h). In each classroom there will be 8 students (4 pairs) and one teacher will supervise 2 classrooms.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Barcelona
-
Hospitalet de Llobregat, Barcelona, Spain, 08907
- Faculty of Nursing
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students enrolled in the compulsory course of the 2nd year of the nursing degree entitled Estades Clíniques I. This subject contains a module called Clinical Skills in which students learn different technical skills with low fidelity simulators (task-trainers).
Exclusion Criteria:
- Not having passed the human anatomy course taught in the 1st year of the nursing degree.
- Not to sign the consent form to participate in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Simcapture PRE
In the PRE intervention group (before the traditional teaching) students will practice in pairs, with the same low fidelity simulator, the blood collection technique without a teacher in the classroom.
In the SimCapture for Skills interface, the procedure of how to perform the technique (sequence of actions) will be developed in checklist format for the student to check step by step.
They will be provided with the same material and classroom time as in traditional teaching (2h).
|
Practice with the SimCapture for Skills interface before the traditional teaching with the teacher in the classroom
|
|
Experimental: Simcapture POST
In the POST intervention group (after the traditional teaching) the students will practice in pairs, with the same low fidelity simulator, the blood collection technique without a teacher in the classroom.
In the SimCapture for Skills interface, the procedure of how to perform the technique (sequence of actions) will be developed in checklist format for the student to check step by step.
They will be provided with the same material and classroom time as in traditional teaching (2h).
|
Practice with the SimCapture for Skills interface after the traditional teaching with the teacher in the classroom
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction and self-confidence acquired by students in both learning spaces.
Time Frame: Immediately after learning with Simcapture and immediately after learning with the teacher in the classroom
|
The Student Satisfaction and Self-Confidence in Learning Scale will be used to evaluate satisfaction and self-confidence, with 12 Likert-rated items (1 -strongly disagree- to 5 -strongly agree-).
|
Immediately after learning with Simcapture and immediately after learning with the teacher in the classroom
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student self-assessment using the technique assessment grid created by the faculty.
Time Frame: During learning with Simcapture or during learning with the teacher in the classroom, through study completion, an average of 3 months
|
Checklist technical skills: Rubric with 76 actions to be performed according to the technical procedure.
The % of actions correctly performed over the total (n/76*100) will be analyzed.
|
During learning with Simcapture or during learning with the teacher in the classroom, through study completion, an average of 3 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Economic costs associated with each type of teaching extrapolating the data to the students enrolled in the subject
Time Frame: Immediately after the learning with Simcapture and with teacher
|
Economic costs
|
Immediately after the learning with Simcapture and with teacher
|
|
Number of times each student can practice the technique with the low-fidelity simulator in both learning spaces.
Time Frame: During learning with Simcapture or during learning with the teacher in the classroom, through study completion, an average of 3 months
|
Number of practice for student
|
During learning with Simcapture or during learning with the teacher in the classroom, through study completion, an average of 3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Raurell-Torreda Marta, RN, PhD, University of Barcelona
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Simcapture Trial
- Facultat Infermeria (Registry Identifier: Universitat de Barcelona)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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