Interprofessional Education and Collaborative Practice Model for Dementia in Acute Care
Primary Purpose
Dementia
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
education
education and workshop
Sponsored by
About this trial
This is an interventional health services research trial for Dementia focused on measuring dementia, hospital, acute care, interprofessional education, interprofessional practice
Eligibility Criteria
Inclusion Criteria:
- healthcare professionals having worked for 3 months or more
- emergency/hospitalized patients with dementia
- patients diagnosed dementia
- scoring 1 or more in Clinical Dementia Rating (CDR).
Exclusion Criteria:
- healthcare professionals working in obstetrics, pediatrics, outpatient, or hemodialysis.
Sites / Locations
- Kaohsiung Medical University Chung-Ho Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
experimental group
control group
Arm Description
The experimental group will not only receive six-hour dementia care course, but also a half-day interprofessional education workshop, maintain a six-month interprofessional practice model, and join interprofessional practice experience-sharing conferences.
The control group will only receive six-hour dementia care course.
Outcomes
Primary Outcome Measures
Change of Dementia Care Knowledge
testing the change of professionals' Dementia Care Knowledge. The minimum value of this scale is 0, and the maximum value is 16.
Higher scores mean having better Dementia Care Knowledge.
Secondary Outcome Measures
Change of dementia self-efficacy scale
testing professionals' dementia self-efficacy. The scale has not developed yet. It will be developed and test the reliability and validity in this study.
mortality rate of hospitalized patients with dementia
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
length of stays of hospitalized patients with dementia
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
the incidence of fall hospitalized patients with dementia
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
the incidence of pain hospitalized patients with dementia
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
score of Beck depression inventory
testing psychological symptoms of hospitalized patients with dementia
score of Cohen-Mansfield Agitation Inventory (CMAI)
testing behavioral symptoms of hospitalized patients with dementia
Full Information
NCT ID
NCT04262973
First Posted
February 4, 2020
Last Updated
February 6, 2020
Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04262973
Brief Title
Interprofessional Education and Collaborative Practice Model for Dementia in Acute Care
Official Title
Interprofessional Education and Collaborative Practice Model for Dementia in Acute Care: Development, Implementation and Evaluation
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2020 (Anticipated)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
July 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The purpose of this study is to develop an interprofessional education and practice model for acute care related to dementia and evaluate its effectiveness of implementation.
Detailed Description
The researchers will recruit participants from a medical center (experimental group) and two regional hospitals (control group) in southern Taiwan. Both the experimental group and the control group will contain 150 healthcare professionals and 64 patients with dementia. Both of the groups will receive a six-hour dementia care course. Then, only the experimental group will receive a half-day interprofessional education workshop, maintain a six-month interprofessional practice model, and join interprofessional practice experience-sharing conferences. The evaluation of outcomes will include the analyses of healthcare professionals' knowledge, attitudes, and self-efficacy of dementia care. The evaluation times are to be before and after the dementia care course and after the six months of interprofessional practice. The other evaluation of outcome is comparison of the outcomes of hospitalized patients with dementia between the two groups before the interprofessional education workshop and after the interprofessional practice.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia
Keywords
dementia, hospital, acute care, interprofessional education, interprofessional practice
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
428 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
experimental group
Arm Type
Experimental
Arm Description
The experimental group will not only receive six-hour dementia care course, but also a half-day interprofessional education workshop, maintain a six-month interprofessional practice model, and join interprofessional practice experience-sharing conferences.
Arm Title
control group
Arm Type
Active Comparator
Arm Description
The control group will only receive six-hour dementia care course.
Intervention Type
Other
Intervention Name(s)
education
Intervention Description
six-hour dementia care course
Intervention Type
Other
Intervention Name(s)
education and workshop
Intervention Description
six-hour dementia care course, half-day interprofessional education workshop, and interprofessional practice
Primary Outcome Measure Information:
Title
Change of Dementia Care Knowledge
Description
testing the change of professionals' Dementia Care Knowledge. The minimum value of this scale is 0, and the maximum value is 16.
Higher scores mean having better Dementia Care Knowledge.
Time Frame
Before education program(pre-intervention), after education program(10 months), after the workshop(10 months), after the six months interprofessional practice(post intervention)[about 8 months]
Secondary Outcome Measure Information:
Title
Change of dementia self-efficacy scale
Description
testing professionals' dementia self-efficacy. The scale has not developed yet. It will be developed and test the reliability and validity in this study.
Time Frame
Before education program(pre-intervention), after education program(10 months), after the workshop(10 months), after the six months interprofessional practice(post intervention)[about 8 months]
Title
mortality rate of hospitalized patients with dementia
Description
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
Time Frame
about 2 years
Title
length of stays of hospitalized patients with dementia
Description
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
Time Frame
about 2 years
Title
the incidence of fall hospitalized patients with dementia
Description
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
Time Frame
about 2 years
Title
the incidence of pain hospitalized patients with dementia
Description
understand the treatment outcomes of hospitalized patients with dementia before the interventions six months and after interventions six months.
Time Frame
about 2 years
Title
score of Beck depression inventory
Description
testing psychological symptoms of hospitalized patients with dementia
Time Frame
about 2 years
Title
score of Cohen-Mansfield Agitation Inventory (CMAI)
Description
testing behavioral symptoms of hospitalized patients with dementia
Time Frame
about 2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
healthcare professionals having worked for 3 months or more
emergency/hospitalized patients with dementia
patients diagnosed dementia
scoring 1 or more in Clinical Dementia Rating (CDR).
Exclusion Criteria:
healthcare professionals working in obstetrics, pediatrics, outpatient, or hemodialysis.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
PEI-CHAO LIN, doctoarte
Phone
886-7-3121101
Ext
2609
Email
pclin@kmu.edu.tw
Facility Information:
Facility Name
Kaohsiung Medical University Chung-Ho Memorial Hospital
City
Kaohsiung city
ZIP/Postal Code
807
Country
Taiwan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pei-Chao Lin, doctorate
Phone
886-7-3121101
Ext
2609
Email
pclin@kmu.edu.tw
12. IPD Sharing Statement
Learn more about this trial
Interprofessional Education and Collaborative Practice Model for Dementia in Acute Care
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