Exploring the Educational Needs of Family Caregivers for Patients with Dementia

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Bibliographic Details
Title: Exploring the Educational Needs of Family Caregivers for Patients with Dementia
Language: English
Authors: Karen L. Franck, Janet Fox, Ann A. Berry, Kristen Johnson, Jessica Taylor, Matt Devereaux
Source: Journal of Human Sciences & Extension. 2025 13(3).
Availability: School of Human Sciences, Mississippi State University. PO Box 9745, Mississippi State, MS 39762. Tel: 662-325-6861; Fax: 662-325-8188; e-mail: jhse@ext.msstate.edu; Web site: https://scholarsjunction.msstate.edu/jhse/
Peer Reviewed: Y
Page Count: 11
Publication Date: 2025
Document Type: Journal Articles
Reports - Research
Descriptors: Caregivers, Caregiver Training, Caregiver Attitudes, Dementia, Alzheimers Disease, Needs Assessment, Online Surveys, Educational Needs, Family Needs, Information Needs, Information Seeking, Access to Information, Information Dissemination, Program Design, Program Evaluation, Nonschool Educational Programs
ISSN: 2325-5226
Abstract: Family members who care for patients diagnosed with Alzheimer's and dementia often face significant stressors and challenges that impact their quality of life. As part of a project to develop Extension educational materials and resources specifically for family caregivers, we conducted an online needs assessment survey with 196 adults in the U.S. Participants identified doctors, the internet, and caregiver support groups as top sources of information about dementia. They were interested in strategies to help them manage stress, address patient behavioral issues, and access locally available resources. Furthermore, they were interested in attending educational programs with other caregivers. These findings provide guidance for Extension professionals to design and tailor educational programs and information to help family caregivers provide optimal care for their loved ones.
Abstractor: As Provided
Entry Date: 2026
Accession Number: EJ1492259
Database: ERIC
Description
Abstract:Family members who care for patients diagnosed with Alzheimer's and dementia often face significant stressors and challenges that impact their quality of life. As part of a project to develop Extension educational materials and resources specifically for family caregivers, we conducted an online needs assessment survey with 196 adults in the U.S. Participants identified doctors, the internet, and caregiver support groups as top sources of information about dementia. They were interested in strategies to help them manage stress, address patient behavioral issues, and access locally available resources. Furthermore, they were interested in attending educational programs with other caregivers. These findings provide guidance for Extension professionals to design and tailor educational programs and information to help family caregivers provide optimal care for their loved ones.
ISSN:2325-5226