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Abstract

Dementia is a neurodegenerative disorder characterized by cognitive decline, significantly impacting caregivers, especially in collectivist societies like India, where caregiving is viewed as a familial duty. Caregivers experience emotional, social, and financial burdens, which result in work productivity loss, absenteeism, presenteeism, and a reduction in quality of life. Furthermore, the financial strain on caregivers, due to medical costs and reduced employment opportunities, adds to the overall burden. This proposal seeks to address these challenges through the development and implementation of structured, community‐based programs and policy reforms.

This care practice proposal is grounded in the theory of stress management and caregiving burden, emphasizing the need for non‐pharmacological interventions such as stress‐reduction techniques and practical training for caregivers. Structured training programs equip caregivers with the necessary skills to manage dementia patients at home more effectively. These programs will focus on stress management, coping strategies, and improving patient care through non‐pharmacological means. Additionally, support groups to provide emotional relief and reduce the isolation that caregivers often experience.

The proposal also highlights the need for systemic policy reforms, particularly regarding insurance coverage. Comprehensive insurance policies that cover home‐based care, respite services, and dementia‐related medical expenses are crucial in mitigating the financial burden on caregivers. This aspect of the proposal aims to inform policy development by ensuring that families have the financial support they need to manage the long‐term care of dementia patients.

The outcomes of this proposal have the potential to inform future research on caregiver stress and dementia care. By reducing caregiver burden and improving patient care through non‐pharmacological interventions, we hypothesize that both caregiver and patient well‐being can be enhanced. Furthermore, the proposed insurance reforms could reduce out‐of‐pocket expenses, thereby improving the quality of life for caregivers and alleviating economic strain on the healthcare system.

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1009240
Business indexing term
Location
Title
Empowering Caregivers of People with Dementia in India: Addressing Financial, Emotional, and Policy Gaps
Author
Dadoo, Niharika 1 ; Prakash, Ajay 1 ; Medhi, Bikash 1 

 Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, Chandigarh, India, 
Publication title
Volume
21
Supplement
S4
Number of pages
3
Publication year
2025
Publication date
Dec 1, 2025
Section
DEMENTIA CARE RESEARCH AND PSYCHOSOCIAL FACTORS
Publisher
John Wiley & Sons, Inc.
Place of publication
Chicago
Country of publication
United States
ISSN
1552-5260
e-ISSN
1552-5279
Source type
Scholarly Journal
Language of publication
English
Document type
Journal Article
Publication history
 
 
Online publication date
2025-12-24
Milestone dates
2025-12-24 (publishedOnlineFinalForm)
Publication history
 
 
   First posting date
24 Dec 2025
ProQuest document ID
3286515966
Document URL
https://www.proquest.com/scholarly-journals/empowering-caregivers-people-with-dementia-india/docview/3286515966/se-2?accountid=208611
Copyright
© 2025. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Last updated
2026-01-02
Database
ProQuest One Academic