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Digital Learning Technology for Dementia Care Training in Long-term Care Professionals

25 de junio de 2026 actualizado por: Yi-Ling Tseng, Tunghai University

Effects of Digital Learning Technology in Dementia Education Programs on Dementia Care Knowledge, Attitudes, and Interprofessional Collaboration Among Long-term Care Professionals

Dementia, including cognitive decline and behavioral and psychiatric symptoms of dementia (BPSD), presents a significant challenge to long-term care systems and family caregivers. While various digital educational resources are available, long-term care professionals often face challenges in practical care skills, communication, and emotional coping when managing individuals with moderate to severe dementia. To address these needs, a dementia education program integrating digital learning technologies was proposed to offer a meaningful, collaborative learning experience.

The purpose of this study was to evaluate the effects of this immersive learning dementia education program on long-term care professionals' dementia care knowledge, attitudes, and interprofessional collaboration competence (as the primary outcome variables).

This study utilized a quasi-experimental, waitlist control group pre- and post-test design. This study utilized a quasi-experimental, waitlist control group pre- and post-test design. Long-term care professionals were recruited from 12 community-based long-term care institutions in Taiwan. Participants were assigned to either the intervention group or the waitlist control group based on the order of enrollment.

The intervention group participated in an 8-hour, 4-unit immersive training program held during non-working hours. The curriculum included: an advanced dementia care lecture and case discussions; Virtual Reality (VR) dementia symptom simulation (using HTC VIVE Flow headsets) followed by reflective debrief; Augmented Reality (AR) interactive skill training (using the MAKAR Viewer mobile app); and experience sharing on ethical and legal issues in dementia care.

The waitlist control group maintained their routine continuing education during the study period and received the identical 8-hour training program after the follow-up assessments were completed.

All participants completed standardized questionnaires at three time points: at baseline (pre-test), immediately following the intervention (post-test), and at a 3-month follow-up. The outcomes measured included dementia care knowledge, dementia care attitudes, and interprofessional collaboration levels.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

150

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Taichung, Taiwán, 4070
        • Tunghai University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria: (1)Must be a registered long-term care professional or care assistant currently employed in a long-term care institution; (2) Provided informed consent and voluntarily agreed to participate in this study; (3) Capable of using digital learning devices, including smartphone applications and virtual reality (VR) headsets.

Exclusion Criteria: (1)Severe visual or hearing impairments that prevent the effective use of digital learning materials or VR headsets; (2)A history of severe motion sickness, vertigo, or epilepsy that could be triggered by immersive virtual reality (VR) experiences.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Intervention Group
Participants received the 8-hour dementia care education program consisting of four sequential modules: (1) advanced dementia care lectures and case discussions, (2) immersive virtual reality (VR) symptom experiences using HTC VIVE Flow headsets followed by reflective group discussions, (3) augmented reality (AR) interactive care skill training via mobile applications combined, and (4) sharing experiences of ethical and legal issues in dementia care.
an 8-hour digital learning dementia care education program
Comparador activo: Control Group
Maintained routine education and completed parallel tests at T0, T1, and T2. The identical 8-hour program was provided to this group after T2 data collection ends.
Maintaind routine education and completed parallel tests at T0, T1, and T2. The identical 8-hour digital learning dementia care program was provided to this group after T2 data collection ends.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Interprofessional collaboration level
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.
Measured using the Collaboration subscale of the Chinese Version of the Assessment of Interprofessional Team Collaboration Scale (AITCS-C), this subscale assessed the extent to which long-term care professionals perceived themselves as team members who listened to and valued all members' perspectives, actively contributed professional insights, and engaged in shared decision-making. It consisted of 8 items rated on a 5-point Likert scale (ranging from 1 = Never to 5 = Always), and the total subscale score ranged from 8 to 40, with higher scores indicating a higher perceived level of interprofessional collaboration within the care team. Subgroup interactions based on occupational categories (healthcare professionals vs. care assistants) were evaluated.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.
Knowledge of dementia care
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.
Measured using the Taiwan Shortened Version of the Dementia Knowledge Assessment Scale (DKAS-s), this scale evaluated long-term care professionals' knowledge level across four distinct dimensions: (1) causes and characteristics of dementia, (2) communication and engagement, (3) dementia care needs, and (4) risk assessment and health promotion. The scale consisted of 16 items utilizing a partial credit scoring method, where each correct answer yielded 1 point, and incorrect or "don't know" responses yielded 0 points. The total score ranged from 0 to 16, with higher total scores indicating a higher level of understanding and knowledge of dementia care, and subgroup interactions based on occupational categories (healthcare professionals vs. care assistants) were evaluated.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.
Attitude toward dementia
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.
Measured using the Dementia Attitude Scale - Chinese Version (DAS-C), this scale evaluated long-term care personnel's attitudes toward individuals with dementia across two primary dimensions: (1) Social Comfort, which encompassed affective and behavioral components, and (2) Dementia Knowledge, which covered the cognitive component. The scale consisted of 17 items scored on a 5-point Likert scale (ranging from 1 = Strongly Disagree to 5 = Strongly Agree). The total score ranged from 17 to 85, with higher total scores indicating a more positive and favorable caregiving attitude toward people living with dementia. Subgroup interactions based on professional categories (healthcare professionals vs. care assistants) were evaluated.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up post-intervention.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Interprofessional collaboration level changes by occupational category
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.
Evaluated the subgroup interaction effect between occupational categories (healthcare professionals vs. care assistants) and time points within the intervention group using Generalized Estimating Equations (GEE). This analysis determined whether the treatment efficacy on interprofessional collaboration degrees (measured via the AITCS-C Collaboration subscale) differed significantly based on the participants' occupational categories.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.
Dementia care knowledge changes by occupational category
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.
Evaluated the subgroup interaction effect between occupational categories (healthcare professionals vs. care assistants) and time points within the intervention group using Generalized Estimating Equations (GEE). This analysis determined whether the treatment efficacy on dementia care knowledge (measured via the DKAS-s) differed significantly based on the participants' occupational categories.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.
Dementia care attitude changes by occupational category
Periodo de tiempo: Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.
Evaluated the subgroup interaction effect between occupational categories (healthcare professionals vs. care assistants) and time points within the intervention group using Generalized Estimating Equations (GEE). This analysis determined whether the treatment efficacy on dementia care attitudes (measured via the DAS-C) differed significantly based on the participants' occupational categories.
Baseline (pre-test), immediately post-intervention, and at a 3-month follow-up.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

25 de agosto de 2025

Finalización primaria (Actual)

8 de junio de 2026

Finalización del estudio (Actual)

8 de junio de 2026

Fechas de registro del estudio

Enviado por primera vez

25 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

25 de junio de 2026

Publicado por primera vez (Actual)

1 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

25 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • KMUHIRB-E(I)-20250272
  • NSTC 114-2515-S-037-001 (Otro número de subvención/financiamiento: This study was supported in part by a grant from the National Science and Technology Council, Taiwan (R.O.C))

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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