Course overview
Low health literacy can lead to missed appointments, medication errors, delayed care, poor uptake of prevention services and avoidable distrust. The challenge is not limited to a person's reading ability. Forms, consent processes, digital channels, clinical language, risk messages and referral systems can all place unreasonable demands on patients, families and communities. Public health teams must identify these barriers, communicate clearly and involve communities in decisions that affect access, safety and health outcomes.
This course equips participants to assess health literacy needs, segment priority audiences and design practical responses. Participants use the CDC Clear Communication Index, plain-language methods, teach-back, co-design principles, asset-based community development and behaviour change models. They learn how to involve community representatives ethically, establish peer education approaches, address misinformation, communicate during health incidents and build interventions that account for language, disability, digital exclusion and trust.
Instruction combines concise technical briefings with realistic cases from primary care, vaccination programmes, maternal health, chronic disease management and community outreach. Participants analyse communication materials, service journeys and community data; practise message development and facilitation techniques; and apply evaluation methods to their own context. Each participant leaves with a health literacy improvement action plan, communication review checklist, stakeholder engagement approach and evaluation framework that can be adapted for a service, programme or population.
The course is suited to public health, health promotion, clinical, social care, NGO and community-facing professionals responsible for improving access to information, preventive services and participation in health decisions.
