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OpenTrials
Completed

NCT Number: NCT05742659

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

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.

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Key information

Conditions

Nasogastric Tube Insertion

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Cheng Kung University Hospital

Tainan, 704, Taiwan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

Treatment and study plan

A mobile-based interactive simulation scheme (MISS)

Other

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

Primary outcomes

  1. 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.

  2. The self-confidence scale (C-scale)

    Time frame: one week

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

Secondary outcomes

  1. System Usability Scale (SUS)

    Time frame: one week

    1-5. One is strongly disagree, and five is strongly agree.

  2. The NASA-TLX (Task load index)

    Time frame: one week

    1-5. One is strongly disagree, and five is strongly agree.

  3. The overall learning satisfaction

    Time frame: one week

    1-5 each. One is strongly disagree, and five is strongly agree. The questionnaire included 20 questions, divided into 11 categories: perceived enjoyment, comparison, diagnosis report, satisfaction, intension to use, perceived usefulness, perceived ease of use, image, output quality, result demonstrability, and cognitive load.

  4. The OSCE (Objective Structured Clinical Examination) test

    Time frame: one week

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

Sponsors and collaborators

Lead sponsor

National Cheng-Kung University Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2020
Study completion
2021
First posted
Feb 24, 2023
Registry last updated
Feb 24, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.