N/A
N=37
Satisfaction With an In-house Developed Nasal Foreign Body Removal Manikin
Satisfaction · Consumer Satisfaction
Bottom Line
View on ClinicalTrials.gov: NCT04901026 ↗Enrolled (actual)
37
Serious AEs
0.0%
Results posted
Apr 2024
Primary outcome: Primary: Satisfaction Scores — 4; 4; 4; 4 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- An in-house manikin (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Prince of Songkla University
- Primary completion
- Jul 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Satisfaction Scores |
4; 4; 4; 4; 5; 4 | — |
Summary
To overcome the issues regarding training in real persons, using a simulated manikin instead of an actual patient or simulated patient is another option with consideration to the training able to be held at any time periods and no issues about minor or serious complications needed to be concerned with. The aim of this study is to devise a low-cost manikin with a specific design to serve all possible needs of end users but still keep its function as necessary for training.
Eligibility Criteria
Inclusion Criteria
- Physicians who hold a MD degree
Exclusion Criteria
- Not want to complete questionnaires
- No experience in a nasal foreign body removal
Data sourced from ClinicalTrials.gov (NCT04901026). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.