- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06032351
Construction and Validation of Dementia Care Management Competency
July 3, 2024 updated by: Huei-Ling Huang, Chang Gung Memorial Hospital
Construction and Validation of Dementia Care Management Competency: From Curriculum Integration to Outcome Evaluation
This study will use the concept of competency-based education to develop an innovative integrated curriculum with EPAs to guide learning and assessment of competency performance to equip students with dementia care management competency and cultivate professionals to meet the social trends and practical needs.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This study will use the concept of competency-based education to develop an innovative integrated curriculum with EPAs to guide learning and assessment of competency performance to equip students with dementia care management competency and cultivate professionals to meet the social trends and practical needs.
The first year is a preparation period for the development of the project, which focuses on developing research tools and teacher empowerment, and evaluating the effectiveness of the control group in implementing conventional teaching methods.
The second year is the program testing, implementation and evaluation period, in which two phases of the intervention is conducted and the post-intervention phase of competency is evaluated.
This study is expected to establish a competency-based innovative and integrated curriculum for dementia care management over a two-year period.
The results of the study will be used as a reference for schools or practices in the development of competency-based curriculum integration.
Study Type
Interventional
Enrollment (Estimated)
190
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Huei-Ling Huang, PhD
- Phone Number: 5803 +886-3-2118999
- Email: hlhuang@gw.cgust.edu.tw
Study Locations
-
-
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Taoyuan, Taiwan, 333
- Recruiting
- Chang Gung University of Science and Technology
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
(1)Be at least 20 years old.
(2)The students are freshmen majoring in the Department of Gerontology and Health Care Management, and taking the course on Dementia care.
(3)Before taking the course on Dementia care, have taken courses on basic geriatric nursing.
(4)voluntary participation
Exclusion Criteria:
- The students who suspension of schooling.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: conventional teaching group
conventional teaching methods
|
The conventional teaching group will receive only traditional classroom teaching course programs.
Other Names:
|
|
Experimental: curriculum integration Group
The curriculum integration group will receive two intervention phases, including an innovation-integrated curriculum for dementia care and an innovation-integrated curriculum for care management with Entrustable Professional Activities (EPAs) to guide learning and assessment of competency performance to equip students with dementia care management competency.
|
The curriculum integration group will receive two intervention phases, including an innovation-integrated curriculum for dementia care and an innovation-integrated curriculum for care management with Entrustable Professional Activities (EPAs), lectures, Situated Simulation Learning, Team-based learning, and Objective Structured Clinical Examination(OSCE).
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographic data of student
Time Frame: The investigators will collect demographic data of students on the day before the start date of the intervention.
|
Include age, gender, education level, areas of studying, etc.
|
The investigators will collect demographic data of students on the day before the start date of the intervention.
|
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Dementia Care Professional Competency Assessment Scale
Time Frame: T0(Baseline), T1(Immediately after the intervention), T2(3 months after the intervention).
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T0(Baseline), T1(Immediately after the intervention), T2(3 months after the intervention).
|
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Problem solving, Teamwork Competency Assessment Scale
Time Frame: T0(Baseline), T1(Immediately after the intervention), T2(3 months after the intervention).
|
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T0(Baseline), T1(Immediately after the intervention), T2(3 months after the intervention).
|
|
Learning Satisfaction Scale
Time Frame: Immediately after the intervention.
|
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Immediately after the intervention.
|
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Performance in a summative OSCE test (OSCE scores)
Time Frame: Immediately after the intervention.
|
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Immediately after the intervention.
|
|
Qualitative interview
Time Frame: The investigators will conduct qualitative interviews using focus groups 3 months after the intervention.
|
Conduct qualitative interviews with the curriculum integration group students, focusing on the effectiveness of the curriculum integration.
|
The investigators will conduct qualitative interviews using focus groups 3 months after the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Huei-Ling Huang, PhD, Chang Gung University of Science and Technology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 27, 2024
Primary Completion (Estimated)
July 31, 2025
Study Completion (Estimated)
July 31, 2025
Study Registration Dates
First Submitted
August 21, 2023
First Submitted That Met QC Criteria
September 4, 2023
First Posted (Actual)
September 13, 2023
Study Record Updates
Last Update Posted (Actual)
July 5, 2024
Last Update Submitted That Met QC Criteria
July 3, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NSTC 112-2410-H-255 -006 -MY2
- NMRPF3N0081 (Other Identifier: Chang Gung University of Science and Technology)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.