- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05131789
Establishment and Application of Dementia Case Management Information System: A Preliminary Study
Establishment and Application of Dementia Case Management Information System: A Preliminary Study - Phase 2
The purpose of this study is to develop and examine the preliminary effects of an information system for facilitating dementia case management in the home setting.
This study is the second phase of the project. The first year is the development stage of the information system. In the second year, the investigators will conduct a pilot study to examine the effectiveness of the case management information system.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The purpose of this study is to develop and examine the preliminary effects of an information system for facilitating dementia case management in the home setting. In the previous research (phase I), a mixed method was used to explore the content of case management and assess the needs of the information system.
This study is the second phase of the project. The first year is the development stage of the information system. Based on the data collected in the previous research (phase I), the content and method of dementia case management will be established by the Delphi method, and then the dementia case management information system will be constructed accordingly. In the second year, the investigators will conduct a pilot study to examine the effectiveness of the case management information system.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Taoyuan, Taiwan, 333
- Chang Gung University of Science and Technology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Dementia Case Managers:
- Be at least 20 years old and could communicate in Chinese or Taiwanese.
- Currently work for dementia center, dementia care center, or Community-Based Dementia Care Center in Taiwan.
Dementia family caregivers:
- Be at least 20 years old and could communicate in Chinese or Taiwanese.
- Primary caregivers
- The people with dementia under care are diagnosed with dementia Clinical Dementia Rating(CDR) 0.5 or higher.
- Live in northern Taiwan(including Taipei, New Taipei, Taoyuan, and Hsinchu).
Exclusion Criteria:
- Dementia Case Managers:
No longer working for dementia center, dementia care center, or Community-Based Dementia Care Center in Taiwan.
- Dementia family caregivers:
The people with dementia under care live in a long-term care facility or nursing home.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Information System Group
The dementia case managers in the experiment group use information system to perform case management.
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The investigators will develop an information system based on the data collected in our previous research, the content and method of dementia case management which will be established by the Delphi method, and then the dementia case management information system will be constructed accordingly.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Dementia Care Professional Competency Assessment Scale
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Dementia Care Professional Competency at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Dementia Care Professional Competency at 1, 3, and 6 months.
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Problem solving, Teamwork Competency Assessment Scale
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Problem solving, Teamwork Competency at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Problem solving, Teamwork Competency at 1, 3, and 6 months.
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Caregiver Preparedness Scale - Professional version
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver Preparedness - Professional at 1,3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver Preparedness - Professional at 1,3, and 6 months.
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Basic information of dementia and family caregivers
Time Frame: The investigators will evaluate before the intervention.
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The investigators will evaluate before the intervention.
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Cohen-Mansfield Agitation Inventory (CMAI)
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline behavioral problems (CMAI) at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline behavioral problems (CMAI) at 1, 3, and 6 months.
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Agitation Management Self-Efficacy Scale (AMSS)
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline caregiver self-efficacy to handle behavioral problems (AMSS) at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline caregiver self-efficacy to handle behavioral problems (AMSS) at 1, 3, and 6 months.
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Activities of daily living (ADL)
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline ADL at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline ADL at 1, 3, and 6 months.
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Instrumental Activities of Daily Living (IADL)
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline IADL at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline IADL at 1, 3, and 6 months.
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Caregiver competence Scale
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver competence at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver competence at 1, 3, and 6 months.
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Caregiver Preparedness Scale - family caregiver version
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver Preparedness - family caregiver at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline Caregiver Preparedness - family caregiver at 1, 3, and 6 months.
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36-item short-form health survey (SF-36)
Time Frame: The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline quality of life (SF-36) at 1, 3, and 6 months.
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The investigators will evaluate before the intervention, and after intervention for 1, 3, and 6 months. Change from Baseline quality of life (SF-36) at 1, 3, and 6 months.
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Qualitative interview
Time Frame: The investigators will conduct qualitative interviews before the intervention, and after intervention for 1 month.
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Conduct qualitative interviews with dementia case managers, focusing on the use of information system.
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The investigators will conduct qualitative interviews before the intervention, and after intervention for 1 month.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Huei-Ling Huang, PhD, Chang Gung University of Science and Technology
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
- ZRRPF3L0041
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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