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Clinical Trials/NCT05742659
NCT05742659CompletedNot Applicable

Effects of Developing a Mobile-based Interactive Simulation Scheme for Assisting the Personalized Hands-on Learning of Nasogastric Tube Insertion: a Randomized Controlled Trial

National Cheng-Kung University Hospital1 site in 1 country73 target enrollmentStarted: August 17, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
73
Locations
1
Primary Endpoint
The self-confidence scale (C-scale)

Study Overview

Brief Summary

A mobile-based interactive simulation scheme (MISS) was proposed and developed to investigate its effects on facilitating hands-on learning of nasogastric tube insertion in undergraduate medical students.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •fifth-year undergraduate medical students
  • •at least 20 years old
  • •without any practical clinical experience

Exclusion Criteria

  • Not provided

Arms & Interventions

control group

No Intervention

experimental group

Experimental

Intervention: A mobile-based interactive simulation scheme (MISS) (Other)

Outcomes

Primary Outcomes

The self-confidence scale (C-scale)

Time Frame: one week

1-5. One is high uncertainty, and five is complete certainty.

The 10-item evaluation questionnaire on Nasogastric tube insertion knowledge

Time Frame: one week

0-100. Zero is the worst, and 100 is the best.

Secondary Outcomes

  • The NASA-TLX (Task load index)(one week)
  • System Usability Scale (SUS)(one week)
  • The overall learning satisfaction(one week)
  • The OSCE (Objective Structured Clinical Examination) test(one week)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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