NCT04262973

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
428

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 4, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 10, 2020

Completed
20 days until next milestone

Study Start

First participant enrolled

March 1, 2020

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2023

Completed
Last Updated

February 10, 2020

Status Verified

February 1, 2020

Enrollment Period

3.4 years

First QC Date

February 4, 2020

Last Update Submit

February 6, 2020

Conditions

Keywords

dementiahospitalacute careinterprofessional educationinterprofessional practice

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (7)

  • Change of dementia self-efficacy scale

    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]

  • mortality rate of hospitalized patients with dementia

    about 2 years

  • length of stays of hospitalized patients with dementia

    about 2 years

  • the incidence of fall hospitalized patients with dementia

    about 2 years

  • the incidence of pain hospitalized patients with dementia

    about 2 years

  • +2 more secondary outcomes

Study Arms (2)

experimental group

EXPERIMENTAL

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.

Other: education and workshop

control group

ACTIVE COMPARATOR

The control group will only receive six-hour dementia care course.

Other: education

Interventions

six-hour dementia care course

control group

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

experimental group

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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).

You may not qualify if:

  • healthcare professionals working in obstetrics, pediatrics, outpatient, or hemodialysis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kaohsiung Medical University Chung-Ho Memorial Hospital

Kaohsiung City, 807, Taiwan

Location

MeSH Terms

Conditions

Dementia

Interventions

Educational Status

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeurocognitive DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Central Study Contacts

PEI-CHAO LIN, doctoarte

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 4, 2020

First Posted

February 10, 2020

Study Start

March 1, 2020

Primary Completion

July 31, 2023

Study Completion

July 31, 2023

Last Updated

February 10, 2020

Record last verified: 2020-02

Locations