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Information, communication, and online tool needs of Hispanic family caregivers of individuals with Alzheimer's disease and related dementias.
Iribarren, Sarah; Stonbraker, Samantha; Suero-Tejeda, Niurka; Granja, Maribel; Luchsinger, José A; Mittelman, Mary; Bakken, Suzanne; Lucero, Robert.
Afiliación
  • Iribarren S; a Department of Biobehavioral Nursing and Health Informatics , University of Washington , Seattle , WA , USA.
  • Stonbraker S; b Columbia University School of Nursing, Columbia University , New York , NY , USA.
  • Suero-Tejeda N; b Columbia University School of Nursing, Columbia University , New York , NY , USA.
  • Granja M; c National Center for Children in Poverty , Mailman School of Public Health, Columbia University , New York , NY , USA.
  • Luchsinger JA; d Departments of Medicine and Epidemiology , Columbia University Medical Center , New York , NY , USA.
  • Mittelman M; e Departments of Psychiatry and Rehabilitative Medicine , New York University School of Medicine , New York , NY , USA.
  • Bakken S; b Columbia University School of Nursing, Columbia University , New York , NY , USA.
  • Lucero R; f Department of Biomedical Informatics , Columbia University , New York , NY , USA.
Inform Health Soc Care ; 44(2): 115-134, 2019.
Article en En | MEDLINE | ID: mdl-29504837
PURPOSE: To identify the information and communication needs of Hispanic family caregivers for individuals with Alzheimer's Disease and Related Dementias (ADRD) and the manner in which online tools may meet those needs. METHODS: We conducted 11 participatory design sessions with 10 English- and 14 Spanish-speaking urban-dwelling Hispanic family caregivers and gathered data using a survey, collage assemblage, and audio and video recordings. Four investigators analyzed transcripts of audio recordings with a coding framework informed by several conceptual models. RESULTS: Participants had an average age of 59.7 years, were mostly female (79.2%), and had cared for a family member with ADRD for an average of 6.5 years. All participants accessed the Internet at least once a week with 75% ≥ daily. Most used the Internet to look up health information. All participants reported caregiver attributes including awareness of the disease symptoms or behaviors. The majority reported information needs/tasks (91.7%), communication needs/tasks (87.5%), and need for online tools (79.2%). CONCLUSION: Hispanic caregivers of individuals with ADRD reported key information and communication needs/tasks. Only Spanish-speaking participants reported Internet and technology use deficits suggesting the requirement for further technology support. Data show a need for online tools to meet the needs of caregivers.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hispánicos o Latinos / Cuidadores / Comunicación / Demencia / Información de Salud al Consumidor Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Inform Health Soc Care Asunto de la revista: INFORMATICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hispánicos o Latinos / Cuidadores / Comunicación / Demencia / Información de Salud al Consumidor Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Inform Health Soc Care Asunto de la revista: INFORMATICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido