# Telemedicine and Cultural Competency in Dementia Care: Mapping Stakeholder Roles in Digital Toolkit Development in SSA: A Systematic Review

## TL;DR

This paper reviews how telemedicine can improve dementia care in Sub-Saharan Africa by involving stakeholders and adapting to cultural needs.

## Contribution

The study maps stakeholder roles in developing culturally tailored telemedicine tools for dementia care in low-resource settings.

## Key findings

- Five core themes emerged from the analysis of 20 studies on digital dementia care in SSA.
- Mobile health tools showed potential when adapted to cultural contexts.
- Engaging caregivers and community leaders improved the relevance and adoption of telemedicine solutions.

## Abstract

Dementia is a growing concern in Sub‐Saharan Africa (SSA), particularly Nigeria, where care is hindered by weak infrastructure, stigma, and limited culturally responsive services. Telemedicine offers promise but faces adoption challenges in low‐resource settings.

To evaluate digital interventions for dementia care in SSA and examine how culturally tailored telemedicine is shaped by stakeholder input, it may reduce caregiver burden and improve care delivery.

Following PRISMA guidelines, 1650 records were screened: across PubMed, Scopus, PsycINFO, and Google Scholar; 20 studies met inclusion criteria. Thematic analysis identified trends across intervention types, populations, and barriers.

Five core themes emerged: barriers to care (30%), telemedicine opportunities (25%), stakeholder involvement (23%), cultural influences (20%) and technological feasibility (17%). Mobile health tools showed potential when culturally adapted. However, poor infrastructure, digital literacy and traditional beliefs constrained adoption. Engaging caregivers, clinicians and community leaders improved solution relevance and uptake.

Culturally informed, co‐designed telemedicine models can strengthen dementia care delivery in SSA, stakeholder‐driven digital models may serve as a scalable blueprint for other low‐resource contexts.

This review incorporated studies that engaged patients, informal caregivers, clinicians, policymakers and community leaders in the codesign and implementation of digital dementia care tools. Their lived experiences and cultural insights informed the development of interventions that are not only technologically feasible but also socially and “culturally appropriate”.