- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07617883
Dementia Management Training Programme for Primary Health Care Providers
Application and Effectiveness of a RE-AIM-Based Dementia Management Competency Training Program for Primary Health Care Providers: A Cluster Randomized Controlled Trial
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Xinying Lin
- Número de teléfono: +86 18965733707
- Correo electrónico: xinyinglin0416@163.com
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
Primary healthcare workers aged 18 years or older
Registered healthcare professionals holding a formal license issued by the national health authority
At least 1 year of work experience
Able to access the internet using a computer, tablet, or mobile phone
Currently working in a participating community health service center or township health center
Willing to participate in the study and provide written informed consent
Exclusion Criteria:
Personnel who do not directly participate in patient disease management, including logistics or auxiliary staff
Interns, trainees, or students
Individuals currently participating in other similar dementia training interventions
Individuals planning to leave their current institution within the next 12 months
Individuals who refuse to participate in the study or decline to provide written informed consent
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Structured Dementia Management Training Group
Participants in this group will receive a 12-week structured blended dementia management competency training program.
The program includes online learning modules, an in-person skills workshop, case-based supervision, and practice tasks designed to improve dementia knowledge, attitudes, practice competency, and dementia management-related behaviors among primary health care providers.
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The intervention is a 12-week blended training program.
During weeks 1-4, participants will complete seven online modules with a total learning duration of approximately 3 hours.
At the end of week 4, participants will attend a 2-hour in-person skills workshop focusing on standardized cognitive screening and assessment.
During weeks 5-12, participants will participate in online case-based supervision every two weeks and complete practice tasks, including cognitive screening records and dementia management case records.
Otros nombres:
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Comparador activo: Self-directed Learning Control Group
Participants in this group will receive self-directed online learning materials related to dementia management.
The materials include knowledge module videos and text-based resources but do not include structured learning tasks, case analysis, knowledge tests, demonstration videos, forum-based support, learning reminders, expert support, toolkits, in-person workshops, or case-based supervision.
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Participants will be provided with online dementia-related learning materials and will arrange their own learning time and place.
No structured completion requirements, assessments, in-person activities, or expert supervision will be provided.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in dementia knowledge score
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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Dementia knowledge will be measured using the Dementia Knowledge Assessment Scale.
The primary outcome is the change in total DKAS score from baseline to immediately after the 12-week intervention.
Higher scores indicate greater dementia knowledge.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in dementia-related attitudes and confidence
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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Dementia-related attitudes and confidence will be measured using the General Practitioners' Attitudes and Confidence Scale for Dementia.
Higher scores indicate more positive attitudes and greater confidence.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Change in dementia management practice competency
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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Dementia management practice competency was measured using the Dementia Management Practice Competency Scale for Primary Care, which was developed by the research team.
Higher scores on the scale indicate greater dementia management practice competency.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Change in self-reported dementia management-related behaviors
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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Participants will report the frequency of dementia management-related behaviors during the past month, including cognitive screening, identification of suspected cognitive impairment, referral recommendation, communication with patients or family members, and dementia-related health education.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Cognitive screening implementation rate
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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The cognitive screening implementation rate will be calculated as the number of patients aged 65 years or older who received cognitive screening divided by the total number of patients aged 65 years or older seen during the same period, multiplied by 100%.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Referral recommendation documentation rate
Periodo de tiempo: Baseline, immediately after the intervention, and 3 months after the intervention
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The referral recommendation documentation rate will be calculated as the number of screen-positive patients with documented referral recommendations divided by the total number of screen-positive patients, multiplied by 100%.
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Baseline, immediately after the intervention, and 3 months after the intervention
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Online course completion rate
Periodo de tiempo: Immediately after the intervention
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The proportion of intervention group participants who complete all online learning modules.
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Immediately after the intervention
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In-person workshop attendance rate
Periodo de tiempo: Immediately after the intervention
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The proportion of intervention group participants who attend the in-person skills workshop.
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Immediately after the intervention
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Practice task completion rate
Periodo de tiempo: Immediately after the intervention
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The proportion of intervention group participants who submit the required screening records and case management records.
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Immediately after the intervention
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Online supervision participation rate
Periodo de tiempo: Immediately after the intervention
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The number of online supervision sessions attended divided by the number of scheduled supervision sessions.
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Immediately after the intervention
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Training satisfaction and acceptability
Periodo de tiempo: Immediately after the intervention
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Satisfaction and acceptability will be assessed using a self-designed questionnaire with Likert-scale items and open-ended questions.
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Immediately after the intervention
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Institutional maintenance of dementia-related practices
Periodo de tiempo: 3 months after the intervention
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Institutional maintenance will be assessed using a questionnaire completed by institutional managers, including whether cognitive screening, result explanation, referral recommendation, or related training continues after the intervention.
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3 months after the intervention
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Barriers and facilitators to implementation and maintenance
Periodo de tiempo: 3 months after the intervention
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Semi-structured interviews will be conducted with intervention group participants and institutional managers to explore implementation experiences, barriers, facilitators, and suggestions for optimization.
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3 months after the intervention
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- K2026-04-027
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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