the What, When, Where, Why of online healthcare information exclusion
Mental Health factors Lack of confidence in device usage Self-exclusion due to lack of motivation (sense of information overload, trust); or multiple illiteracies: 3Rs, health, IT, information. Articulation of MY health information needs Health literacy (and others) still emerging as a discipline Lack of time to focus on 'my' health due to other constraints and social pressures: duties / work Ethics: Primacy of message? My health or forest logging, over-fishing, selling x,y,z ? | Physical health factors (mobility, senses, ableness ... Inverse Care Law) Geographic issues - terrain remoteness Non-existent or poor broadband services No access to energy supply Quality and safety concerns Need for more research - change studies, innovation. Media modalities: paper->digital, speech (theatre?)->digital ... Design, Usability Grammatical/reading age checks Individual's understanding of the benefits of online healthcare information. |
No spare - individual - income for online services due to family welfare - food ... Languages not available Cultural factors, negative attitudes Personal space in group settings (privacy, concentration, engagement) Articulation of MY family's health information needs Availability of Community initiatives shared access schemes? | Policies / Funding of telecoms infrastructure: community - industry - gov collaboration & partnership* 'Market' conditions - governance Being 'permitted' to have access, use of devices - girls/women. Being voluntarily displaced from local community by work (continuity) Government control of access to services - political fire-walls ('noise'?) Use of pay-walls Incarceration Loss/Dispossession: Refugees - Disasters Deliberate publication of fake-(health) news. Gov & Corp. control of this and advertising. |
Open to suggestions for any additions ...?
Prompt: HIFA message.
*See also previous post:
https://hodges-model.blogspot.com/2020/04/book-third-pillar.html