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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04262973
Other study ID # KMUHIRB-SV(1)-20170070
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2020
Est. completion date July 31, 2023

Study information

Verified date February 2020
Source Kaohsiung Medical University Chung-Ho Memorial Hospital
Contact PEI-CHAO LIN, doctoarte
Phone 886-7-3121101
Email pclin@kmu.edu.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 428
Est. completion date July 31, 2023
Est. primary completion date July 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
education
six-hour dementia care course
education and workshop
six-hour dementia care course, half-day interprofessional education workshop, and interprofessional practice

Locations

Country Name City State
Taiwan Kaohsiung Medical University Chung-Ho Memorial Hospital Kaohsiung city

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Medical University Chung-Ho Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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.
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 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. 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 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. about 2 years
Secondary 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. about 2 years
Secondary 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. about 2 years
Secondary 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. about 2 years
Secondary score of Beck depression inventory testing psychological symptoms of hospitalized patients with dementia about 2 years
Secondary score of Cohen-Mansfield Agitation Inventory (CMAI) testing behavioral symptoms of hospitalized patients with dementia about 2 years
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