- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06574607
Effects of a Contextual Decision-making Materials on Junior Nurses in Traumatic Learning Performance
Effects of a Contextual Decision-making Learning Materials on Nurses in Two Years Learning Performance for Abdominal and Pelvic Traumatic Severe Bleeding Care
Trauma leading to severe bleeding is one of the reasons for the high mortality rate in trauma patients, resulting in multiple and complex injuries from various accidental mechanisms. However, patients with abdominal-pelvic trauma accidents rank among the top three common accidents in the emergency department. There is a potential for both trauma and severe internal bleeding, making the care of such patients even more challenging. Currently, trauma nursing education focuses on emergency medical care, and teaching on the care of abdominal-pelvic trauma occupies only a small part of the entire nursing curriculum.
In addition to insufficient knowledge teaching in emergency trauma medical care, learning relies heavily on the arrangement of clinical internships, and obtaining practical experience in the care of abdominal-pelvic trauma is often difficult. In the current era of thriving digital learning, allowing learning to be more diverse and unrestricted by time and location, it is essential to integrate appropriate guiding strategies alongside digital technology to make learning more efficient and promote meaningful learning.
Therefore, this study introduces decision trees into an interactive scenario-based learning environment for the care of severe bleeding due to abdominal-pelvic trauma. The decision tree is coupled with a decision-making strategy, utilizing the relationships between leaf nodes to guide learners in clarifying their misconceptions, ultimately leading them to make appropriate decisions to reach the final nodes and solve problems.
To understand the effectiveness of this study, a real experimental research design is adopted to investigate the impact of introducing decision tree-based interactive teaching materials on the care of severe bleeding in abdominal-pelvic trauma situations on the professional knowledge, self-efficacy, clinical reasoning assessment ability, and technology acceptance of surgical nursing students over a two-year period. It is hoped that this interactive teaching material for the care of severe bleeding in abdominal-pelvic trauma scenarios will enhance learners' professional knowledge, self-efficacy, clinical reasoning assessment, and technology acceptanc.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 100
- Taiwan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Holding a nursing license, employed, and having job registration in the same institution.
- Those who are willing to participate in this study, are informed, and have provided consent by signing the informed consent form
Exclusion Criteria:
- Those who have completed a service period of more than two years
- Those who refuse to participate in this study.
- Non-Surgical Department ward nurses
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
|
Using severe bleeding from abdominal-pelvic trauma as a scenario case, implementing decision-making teaching strategies to guide learners, and examining the intervention through this research
|
|
Active Comparator: control group
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Teaching with scenario-based interactive materials without incorporating any teaching strategies
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The effect of "Interactive Educational Material for Decision-Making"intervention program on Abdominal and Pelvic Traumatic Severe Bleeding care knowledge learning outcome
Time Frame: up to 1 month
|
TThe changes of Questionnaire score of Abdominal and Pelvic Traumatic Severe Bleeding care knowledge, Questionnaire including: Abdominal and Pelvic Traumatic Severe Bleeding knowledge Scores range from 0 to 15, with higher scores representing higher knowledge of Abdominal and Pelvic Traumatic Severe Bleeding care |
up to 1 month
|
|
The effect of "Interactive Educational Material for Decision-Making"intervention program on Abdominal and Pelvic Traumatic Severe Bleeding care Technology Acceptance learning outcome
Time Frame: up to 1 month
|
The changes of Questionnaire score of Abdominal and Pelvic Traumatic Severe Bleeding care Technology Acceptance, Questionnaire including: Technology Acceptance Scale:Scores range from 1 to 5, with higher scores representing better Technology Acceptance. |
up to 1 month
|
|
The effect of "Interactive Educational Material for Decision-Making"intervention program on Abdominal and Pelvic Traumatic Severe Bleeding care Clinical Reasoning Evaluation Simulation learning outcome
Time Frame: up to 1 month
|
The changes of Questionnaire score of Abdominal and Pelvic Traumatic Severe Bleeding care Clinical Reasoning Evaluation Simulation , Questionnaire including: Clinical Reasoning Evaluation Simulation Tool(CREST): Scores range from 0 to 100, with higher scores representing more positive Clinical Reasoning Evaluation beliefs. |
up to 1 month
|
|
The effect of "Interactive Educational Material for Decision-Making"intervention program on Abdominal and Pelvic Traumatic Severe Bleeding care self-efficacy learning outcome
Time Frame: up to 1 month
|
The changes of Questionnaire score of Abdominal and Pelvic Traumatic Severe Bleeding care self-efficacy will be measured, Questionnaire including: Self-Efficacy Scale:Scores range from 1 to 5, with higher scores representing better self-efficacy. |
up to 1 month
|
Collaborators and Investigators
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202304128RIND
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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