Patient education is one of the most powerful things nurses do. When people understand their condition, their medicines and how to look after themselves, they are more likely to recover well, avoid complications, manage long-term conditions, and stay out of hospital. Yet research consistently shows that patients forget a large share of the medical information they are given, often almost immediately, and that much of what they do remember is remembered incorrectly. Low health literacy is common in every country, including among well-educated people when they are ill, frightened or overwhelmed.
Good patient education is not about delivering as much information as possible. It is about making sure people understand what matters most to them, can act on it, and feel confident to ask questions. This complete guide explains how adults learn, what health literacy means, how to assess learning needs, the teach-back method, plain language, using written, visual and digital materials, cultural and language considerations, motivating behaviour change, teaching families and carers, discharge education, and how to document and evaluate education.
Imagine a 63-year-old man being discharged after a heart attack. In the 20 minutes before his taxi arrives, a busy nurse hands him a stack of leaflets and explains five new medicines, a cardiac rehabilitation referral, warning symptoms, driving rules and a follow-up appointment. He nods and says he understands. In the taxi, he cannot remember which tablet is for what. At home, he stops one of the medicines because it makes him dizzy. Two weeks later he is readmitted. He was told everything. He understood almost none of it. The problem was not him, and it was not the nurse’s intention. The problem was how the teaching was done.
Why patient education matters
Effective patient education is associated with:
- Better self-management of long-term conditions such as diabetes, heart failure, asthma and COPD.
- Safer use of medicines and fewer medication errors at home.
- Fewer emergency visits and hospital readmissions.
- Earlier recognition of warning signs and complications.
- Better recovery after surgery.
- Reduced anxiety and greater confidence.
- More informed decision-making and shared decision-making.
- Improved patient satisfaction and trust.
Patient education is also an ethical and often a legal duty, linked to informed consent and patients’ rights to information about their care. Professional codes, including the International Council of Nurses Code of Ethics, recognise nurses’ responsibility to provide information that people need to make decisions and maintain their health.
Why patients forget
Understanding why information is not retained helps nurses teach more effectively:
- Too much information at once: working memory can hold only a few items at a time.
- Stress and anxiety: illness, pain, fear and unfamiliar environments reduce the ability to absorb information.
- Medical jargon: unfamiliar terms are quickly forgotten or misunderstood.
- Physical factors: pain, fatigue, medicines that affect concentration, hearing and vision problems.
- Cognitive impairment: delirium, dementia or learning disability.
- Timing: teaching given in a rush at discharge, when people are focused on going home.
- Relevance: information that does not connect to what the person cares about is less likely to be remembered.
- Health literacy and language barriers.
How adults learn
Adult learning theory, often associated with Malcolm Knowles’ concept of andragogy, suggests that adults learn best when:
- They understand why they need to learn something.
- Learning builds on their existing experience and knowledge.
- They are involved in planning and directing their learning.
- The information is relevant to their immediate problems and goals.
- Learning is practical and problem-centred rather than abstract.
- They feel respected and in control.
In practice, this means starting with what the patient already knows and wants to know, connecting new information to their daily life, and focusing on practical skills.
Domains of learning
- Cognitive: knowledge and understanding, such as knowing what a medicine is for.
- Psychomotor: practical skills, such as using an inhaler, injecting insulin or changing a dressing.
- Affective: attitudes, beliefs, feelings and motivation, such as confidence to manage a condition or willingness to change a habit.
Effective education addresses all three. A patient may know how insulin works but be too frightened to inject it, or may be able to perform a skill without understanding when to seek help.
Health literacy
Health literacy is the ability to find, understand, evaluate and use health information and services to make decisions about health. It includes reading and numeracy skills, but also the ability to navigate health systems, communicate with professionals, and judge the reliability of information.
Low health literacy is common worldwide. Surveys in several high-income countries have found that a substantial proportion of adults have limited health literacy, and rates are higher among older adults, people with lower levels of formal education, people with limited proficiency in the local language and people from disadvantaged communities. However, anyone can struggle with health information, especially when unwell or stressed.
Limited health literacy is linked to poorer health outcomes, more hospital admissions, less use of preventive services, poorer medication use and higher mortality among older adults.
Universal precautions for health literacy
Because it is impossible to tell someone’s health literacy just by looking at them, and because people often hide difficulties out of embarrassment, experts recommend a “universal precautions” approach: communicate clearly with everyone, rather than trying to identify who needs extra help. This includes using plain language, limiting information to key points, using teach-back and providing clear written materials for all patients.
Signs that someone may be struggling
- Saying “I’ll read this later” or “I forgot my glasses”.
- Bringing a family member to read for them.
- Not asking any questions.
- Missing appointments or not following instructions.
- Identifying medicines by colour or shape rather than name.
- Incomplete forms.
These signs should prompt a respectful, supportive approach rather than judgement.
Assessing learning needs
Before teaching, assess:
- What the person already knows and believes about their condition and treatment.
- What they want to know and what worries them most.
- What they need to know to stay safe, the essential “survival skills”.
- Readiness to learn: physical state, pain, anxiety, emotional readiness.
- Barriers: language, vision, hearing, cognition, literacy, cultural factors, financial constraints.
- Preferred learning style: some people prefer to read, others to watch a demonstration, listen, or practise hands-on.
- Who else should be involved: family members or carers who will help at home.
- Practical circumstances: living situation, access to food, medicines and transport, and daily routine.
Asking open questions such as “What do you know about your condition?” and “What concerns you most about going home?” helps shape teaching around the person.
Plain language: how to explain clearly
- Use everyday words: “high blood pressure” rather than “hypertension”; “kidney” rather than “renal”; “swelling” rather than “oedema”; “take with food” rather than “administer post-prandially”.
- Explain necessary medical terms simply, if the patient will hear them again.
- Use short sentences and an active voice.
- Focus on two or three key messages at a time, starting with the most important.
- Be specific: “Take one tablet in the morning with breakfast” rather than “Take once daily”.
- Explain the why: people are more likely to follow advice they understand.
- Use numbers carefully: natural frequencies (“2 out of 100 people”) are easier to understand than percentages or relative risks.
- Use analogies and examples that connect to everyday life.
- Slow down and pause to allow questions.
- Avoid acronyms and abbreviations.
The teach-back method
Teach-back is one of the most effective, evidence-based techniques for confirming understanding. It involves asking patients to explain in their own words what they have been told, or to demonstrate a skill. It is not a test of the patient; it is a check of how well the nurse has explained.
How to use teach-back
- Explain one key concept in plain language.
- Ask the patient to explain it back, using a non-shaming question such as: “I want to make sure I explained this clearly. Can you tell me how you are going to take this new medicine when you get home?” or “When you get home, your wife will ask what the nurse said. What will you tell her?”
- If the explanation is incomplete or incorrect, explain again in a different way, and check again.
- Repeat until the patient can explain correctly.
Avoid closed questions such as “Do you understand?” or “Any questions?”, which usually lead to “yes” and “no” regardless of actual understanding.
For practical skills, “show-me” works similarly: ask the patient to demonstrate using an inhaler, injecting insulin or checking blood glucose, and correct technique gently.
Teach-back takes only a minute or two once practised, and studies show it improves understanding, self-care and, in some conditions, readmission rates.
Chunk and check
Rather than delivering all the information at once, break it into small chunks, teaching one key point at a time and checking understanding with teach-back before moving on. This reduces overload and makes it easier to correct misunderstandings early.
Written materials
Written information reinforces verbal teaching and gives patients something to refer to at home. To be effective, written materials should:
- Be written in plain language at a reading level accessible to most adults.
- Use short sentences, bullet points and clear headings.
- Focus on actions: what to do, when and how.
- Use a clear font size (at least 12 point, larger for older readers) and plenty of white space.
- Include simple pictures or diagrams that support the message.
- Be available in the languages commonly spoken by patients.
- Be tested with patients before wide use.
- Include contact details and when to seek help.
Personalise materials by highlighting or writing down the key points for the individual patient, such as their specific medicine times or warning signs. Never rely on leaflets alone: handing over paper is not the same as teaching.
Visual aids, demonstrations and practice
Many people learn better with pictures, models, videos and hands-on practice. Effective tools include:
- Medicine charts with pictures and times of day.
- Anatomical models and diagrams.
- Short videos demonstrating skills.
- Practice devices such as demonstration inhalers and injection pens.
- Pictograms for people with low literacy or language barriers.
Practical skills should be demonstrated, then practised by the patient with feedback, ideally more than once before discharge.
Digital health education
Apps, websites, text message programmes, telehealth and online videos offer new ways to educate and support patients. They can provide information at the patient’s own pace, send reminders and allow remote monitoring. However, not all digital resources are reliable, and digital exclusion affects many older adults, people on low incomes, people in rural areas and people with limited digital skills. Recommend trusted sources, check that patients can access and use the tools, and always offer non-digital alternatives. Help patients evaluate online information and generative AI chatbots critically, encouraging them to check with healthcare professionals.
Culture, language and patient education
Culture shapes beliefs about health and illness, how information is shared, the role of family in decisions, dietary practices, religious observances, and attitudes to medicines and traditional remedies. Culturally responsive education involves:
- Asking about patients’ beliefs, practices and preferences rather than making assumptions.
- Adapting advice to fit cultural practices, for example dietary advice based on traditional foods, or medicine timing around religious fasting.
- Respecting the role of family while ensuring the patient’s own voice is heard.
- Using professional interpreters, not family members, especially children, for important information.
- Providing translated materials that are culturally adapted, not just literally translated.
- Working with community health workers and peer educators who share patients’ language and culture.
Working with interpreters
- Brief the interpreter beforehand about the purpose of the session.
- Speak directly to the patient, not the interpreter.
- Use short sentences and pause regularly.
- Use teach-back through the interpreter.
- Allow extra time.
Motivating behaviour change
Much patient education aims to support behaviour change: taking medicines regularly, stopping smoking, changing diet, increasing activity, monitoring symptoms. Information alone rarely changes behaviour. Effective approaches include:
Motivational interviewing
Motivational interviewing is a collaborative, person-centred way of talking that strengthens a person’s own motivation for change. Core skills, often summarised as OARS, are:
- Open questions: “What would you like to be different about your health?”
- Affirmations: recognising strengths and efforts.
- Reflective listening: reflecting back what the person says to show understanding.
- Summaries: drawing together what has been discussed.
Rather than telling people what to do, motivational interviewing helps them explore their own reasons for change, resolve ambivalence and choose their own goals.
Goal setting
Help patients set specific, realistic, small goals, such as “walk for 10 minutes after lunch five days this week”, rather than vague aims like “exercise more”. Achieving small goals builds confidence (self-efficacy).
Addressing barriers
Ask what might get in the way, such as cost, side effects, work schedules, family responsibilities or fear, and problem-solve together.
Ongoing support
Follow-up calls, support groups, self-management programmes and peer support help sustain change over time.
Teaching families and carers
Family members and carers often play a central role in managing medicines, recognising warning signs and supporting recovery. With the patient’s consent, involve them in education sessions, teach them practical skills, provide them with written information and contacts, and acknowledge the stress of caring. Carers of people with dementia, stroke or complex needs may need extra training and support.
Discharge education
The transition from hospital to home is a high-risk time. Effective discharge education:
- Starts early, ideally from admission, rather than in the final hour.
- Focuses on key survival skills: medicines (what, when, why, side effects), warning signs and what to do, activity and diet, wound or device care, and follow-up appointments.
- Uses teach-back for each key point.
- Provides a clear, written summary including an up-to-date medicine list and contact numbers.
- Involves family and carers.
- Checks practical arrangements: can the patient get their medicines, equipment and transport to appointments?
- Includes follow-up, such as a phone call within a few days of discharge.
A simple framework for warning signs is a traffic light plan: green (doing well, continue usual care), amber (warning signs, contact a nurse, pharmacist or healthcare provider) and red (emergency, call emergency services).
Patient education for specific groups
Children and young people
Use age-appropriate language, play, pictures and stories. Involve parents, but also speak directly to children and adolescents. Teenagers need increasing independence and confidential opportunities to ask questions.
Older adults
Allow extra time, minimise background noise, check hearing aids and glasses, use larger print, and involve carers where appropriate. Do not assume older people cannot learn new skills.
People with cognitive impairment or learning disabilities
Use simple language, pictures, repetition and routine. Easy-read materials, involvement of carers and reasonable adjustments, such as longer appointments, help.
People with sensory impairments
Use large print, braille or audio formats for people with visual impairment, and sign language interpreters, written information and clear lip-reading conditions for people who are deaf or hard of hearing.
Documenting patient education
Documentation shows what education was provided, supports continuity and is part of the legal record. Record:
- What was taught, and by what methods.
- Who was present (patient, family, interpreter).
- Materials provided.
- The patient’s response, including teach-back results and skill demonstrations.
- Any barriers identified and how they were addressed.
- Further education needed and plans for follow-up.
Evaluating patient education
Evaluation asks whether the education achieved its goals. Short-term evaluation includes teach-back and skill demonstration. Longer-term evaluation may look at self-management, adherence, symptom control, readmissions and patient-reported confidence. Feedback from patients helps improve materials and teaching methods.
Overcoming common barriers for nurses
- Lack of time: integrate teaching into routine care, such as explaining medicines while giving them. Teach-back takes only a minute or two and saves time by preventing problems later.
- Interruptions: choose quieter times and places where possible.
- Lack of materials: advocate for high-quality, plain-language materials in relevant languages, and share good resources with colleagues.
- Lack of training: seek training in health literacy, teach-back and motivational interviewing.
- Short hospital stays: start education early and link with community services for follow-up.
Teaching about medicines: a practical script
Medicines are one of the most important and most misunderstood areas of patient education. A simple structure for each medicine helps patients remember:
- Name: “This is called amlodipine.”
- Purpose: “It lowers your blood pressure, which protects your heart and brain.”
- How and when: “Take one tablet each morning, with or without food.”
- How long: “This is a long-term medicine. Keep taking it even when you feel well, unless your healthcare provider tells you to stop.”
- Common side effects and what to do: “Some people get swollen ankles. If that happens, tell your nurse or pharmacist; do not just stop it.”
- Warning signs: “If you feel faint or very dizzy, sit down and contact us.”
- Check: “Can you tell me what this tablet is for and when you will take it?”
For patients on several medicines, a personalised medicine chart showing each medicine, its purpose, and the time of day to take it, with a tick box for each dose, is often more useful than individual leaflets. Encourage patients to bring all their medicines to appointments for a “brown bag” review, and to keep an up-to-date list on paper or their phone.
Teaching practical skills
Skills such as using inhalers, injecting insulin, checking blood glucose, managing stoma care, caring for wounds or using a peak flow meter require more than verbal explanation. A proven sequence is:
- Explain the purpose of the skill and why each step matters.
- Demonstrate the whole skill at normal speed.
- Demonstrate again slowly, explaining each step.
- Let the patient talk you through it while you perform it.
- Let the patient perform it while you watch and give feedback.
- Repeat practice on different occasions until the patient is confident and accurate.
Studies of inhaler technique show that a large proportion of patients use their inhalers incorrectly, which significantly reduces how much medicine reaches the lungs. Checking technique at every opportunity, not just once, is one of the simplest high-impact interventions nurses can make.
Patient education is closely linked to shared decision-making, a process in which professionals and patients make decisions together, based on the best available evidence and the patient’s values and preferences. It is particularly important when there is more than one reasonable option, such as choosing between treatments for prostate cancer, deciding whether to start a preventive medicine, or planning end-of-life care. Nurses support shared decision-making by explaining options and their benefits and risks clearly, using decision aids where available, helping patients clarify what matters most to them, and making sure their preferences are communicated to the wider team. A helpful framework is the three questions patients can ask: “What are my options? What are the possible benefits and risks of each option? How likely are these benefits and risks to happen to me?”
Communicating risk
Many patients struggle to understand risk, and the way risk is presented strongly influences decisions. Good practice includes:
- Using absolute numbers (“this medicine reduces the chance of a stroke from 4 in 100 to 3 in 100”) rather than relative risk alone (“reduces stroke by 25 percent”).
- Using the same denominator when comparing risks (“2 in 100 versus 5 in 100”).
- Presenting both benefits and harms.
- Using visual aids such as pictographs showing 100 figures.
- Avoiding vague words like “rare” or “common” without numbers, since people interpret them very differently.
Group education and self-management programmes
Group education, such as structured education programmes for diabetes, cardiac and pulmonary rehabilitation, antenatal classes and self-management courses for long-term conditions, can be highly effective. Groups allow patients to learn from each other, share experiences, reduce isolation and build confidence. Many programmes are led or co-led by nurses, and some are delivered by trained peer educators living with the same condition. Nurses can support attendance by explaining the benefits, addressing barriers such as transport or work, and following up with patients who do not attend.
Health education in the community
Beyond individual patients, nurses educate communities through schools, workplaces, religious venues, community groups, radio and social media. Community health education addresses topics such as vaccination, nutrition, hygiene, maternal and child health, mental health, sexual health and prevention of non-communicable diseases. Working with trusted community leaders, using local languages and examples, and listening to community concerns, rather than simply delivering messages, makes health education more effective. Misinformation, particularly online, is a growing challenge; nurses are among the most trusted sources of health information and can counter it by engaging respectfully, acknowledging concerns and offering accurate, accessible information.
Teaching for common conditions: key messages
Every condition has its own essential knowledge. Some examples of the “must know” points nurses commonly teach:
- Diabetes: what blood glucose targets mean, how to recognise and treat low blood sugar, sick-day rules, foot care, and the importance of regular checks for eyes, kidneys and feet. See our type 2 diabetes guide.
- Heart failure: daily weighing, recognising fluid build-up, fluid and salt guidance, and when to seek help for breathlessness or rapid weight gain.
- Asthma and COPD: correct inhaler technique, the difference between preventer and reliever inhalers, recognising worsening symptoms, and following a written action plan.
- Anticoagulants: taking doses consistently, recognising bleeding, interactions with other medicines and foods, and informing other professionals.
- After surgery: wound care, signs of infection, pain management, mobility, and when to resume normal activities.
- New parents: feeding, safe sleep, recognising illness in a newborn, and maternal warning signs after birth.
- Mental health: understanding the condition, how treatments work, early warning signs of relapse, and where to get help in a crisis.
Condition-specific teaching should still follow the same principles: prioritise, use plain language, check understanding and personalise.
The emotional side of learning
A new diagnosis often brings shock, grief, fear and denial. People may not be ready to learn practical details while they are still absorbing the news. Recognising emotional readiness is part of good teaching. Acknowledge feelings (“This is a lot to take in”), give essential safety information first, and offer to return to other topics later. Some people cope by wanting every detail; others want only the minimum. Respect these differences. Over time, as people adjust, they often become eager to learn more. Linking patients with others who live with the same condition can be particularly powerful at this stage.
Building self-efficacy
Self-efficacy is a person’s belief in their ability to succeed in a specific task, such as managing their diabetes or giving their own injections. It is one of the strongest predictors of whether people take on new health behaviours. Nurses build self-efficacy by:
- Mastery experiences: letting patients practise skills successfully, starting with small steps.
- Role models: sharing examples of others like them who have succeeded.
- Encouragement: giving specific, genuine praise for effort and progress.
- Managing anxiety: helping people interpret nervousness as normal rather than a sign they cannot cope.
Patients who leave hospital saying “I can do this” are far more likely to manage well at home than those who leave with a folder of information but no confidence.
Nurses as learners too
Patient education skills can be developed throughout a career. Watching experienced colleagues, asking for feedback on teaching, attending courses in health literacy and motivational interviewing, and reflecting on what worked and what did not all help. Asking patients directly, “Was there anything I explained that was confusing?” provides valuable insight. Nurses who teach well often say they learn as much from patients as patients learn from them.
Common mistakes in patient education
- Information dumping: giving everything at once, usually at discharge. Prioritise and spread teaching over the stay.
- Asking “Do you understand?”: almost everyone says yes. Use teach-back instead.
- Relying on leaflets alone: written materials support teaching but do not replace it.
- Using jargon without noticing: words like “chronic”, “negative result”, “NPO” or “titrate” can confuse or alarm.
- Ignoring the family: the person managing medicines at home may not be the patient.
- Talking at patients rather than with them: education is a conversation, not a lecture.
- Assuming understanding from education level: even highly educated people struggle when ill or anxious.
- Not following up: understanding and confidence often fade without reinforcement.
A worked example: teaching a new inhaler
Mrs B, aged 70, has just been diagnosed with COPD and prescribed a new inhaler. The nurse begins by asking what she knows about COPD and how she feels about using an inhaler. Mrs B says she is worried she will do it wrong. The nurse explains in plain language that the inhaler opens her airways to make breathing easier, then demonstrates the technique with a placebo device, explaining each step. Mrs B tries it while the nurse watches, and the nurse notices she breathes in too fast. The nurse gently shows her again and Mrs B tries again, this time correctly. The nurse then asks, “Can you tell me when you will use this inhaler and what you will do if your breathing gets worse?” Mrs B answers accurately. The nurse writes the key points on a simple action plan, invites Mrs B’s daughter to the next session, and records the teaching and teach-back result. At the next visit, the nurse checks technique again. This short, focused sequence is more effective than a long lecture or a stack of leaflets.
Measuring health literacy in practice
Formal health literacy assessment tools exist, such as short screening questions and validated questionnaires, and they are useful in research and service planning. In everyday clinical practice, however, the universal precautions approach is usually more practical than formal testing. One simple, widely used screening question is: “How confident are you filling out medical forms by yourself?” Answers of “somewhat”, “a little” or “not at all” suggest the person may benefit from additional support. Whatever the result, every patient benefits from clear, plain-language communication.
Creating a learning-friendly environment
The setting matters as much as the message. Busy wards, noisy clinics and rushed conversations at the bedside make learning difficult. Where possible, choose a quiet moment and place, sit down at the patient’s eye level, make sure they are comfortable and not in pain, close curtains or doors for privacy, and turn off televisions or other distractions. Make sure the patient has their glasses and hearing aids. Sitting down, even briefly, makes conversations feel less rushed and more respectful, and research suggests patients perceive nurses who sit as spending more time with them.
Organisational support for patient education
Individual nurses can teach well, but organisations shape whether good patient education is possible. Helpful organisational measures include training all staff in health literacy and teach-back, providing high-quality plain-language and translated materials, ensuring access to professional interpreters, building education into care pathways and electronic records, protecting time for discharge teaching, employing specialist nurse educators for complex conditions, involving patients in designing materials, and measuring outcomes such as patient understanding and readmissions. Health systems that treat patient education as a core part of care, rather than an optional extra, see better outcomes and more confident patients.
Key messages
- Patients forget much of what they are told; focus on what matters most.
- Assume everyone benefits from clear, plain-language communication.
- Use teach-back and show-me instead of “Do you understand?”
- Break information into small chunks and check understanding after each.
- Combine verbal teaching with written, visual and hands-on methods.
- Respect culture and language, and use professional interpreters.
- Support motivation and confidence, not just knowledge.
- Start discharge teaching early, involve families and arrange follow-up.
- Document what was taught and how well it was understood.
Every conversation with a patient is a chance to teach. Small, well-planned moments of teaching, repeated over time, add up to people who understand their health and feel able to manage it.
Teaching over the phone and by video
Telehealth has become a common way to follow up patients and provide education. Without face-to-face cues, it is even more important to speak slowly, use plain language, check understanding frequently with teach-back, and ask patients to show devices or medicines to the camera where possible. Confirm the patient’s identity and privacy at the start, make sure they have their medicines and materials to hand, and send a written summary afterwards by a method they can access. Offer an in-person visit when remote education is not working well.
When patients and families leave a conversation able to say what they will do, why it matters and when to ask for help, education has done its job.
Frequently asked questions
How much information should I give?
Focus on the two or three most important things the patient needs to know and do, check understanding, and add more as they are ready.
What if the patient refuses education?
Explore why. They may be anxious, in pain, overwhelmed or prefer a family member to be present. Offer later opportunities and written information, and document the conversation.
Is it patronising to use teach-back?
Not if done respectfully. Framing it as checking your own explanation makes it comfortable for patients.
Can I use family members as interpreters?
Professional interpreters should be used for important clinical information. Family members may be used for simple conversations if the patient prefers, but never children for clinical matters.
How do I teach someone who cannot read?
Use verbal explanations, pictures, demonstrations, colour coding, pictograms and teach-back, and involve family members the patient trusts.
But how can I teach properly with so little time?
Time pressure is real. But effective education is not about long sessions; it is about focusing on what matters most and checking understanding. Use every interaction as a teaching moment, prioritise survival skills, use teach-back for the key points, involve families, and make sure follow-up is arranged. Advocate within your organisation for protected time for discharge education, specialist educators for complex conditions, and good-quality materials. A few minutes of effective teaching can prevent days in hospital.
Your next step: On your next shift, replace “Do you understand?” with a teach-back question for at least three patients, such as “Can you tell me in your own words how you will take this medicine at home?”, and notice what you learn.
Related: Medication safety: the complete guide · Nursing ethics: the complete guide
Sources: World Health Organization (health literacy and health promotion resources), Agency for Healthcare Research and Quality (Health Literacy Universal Precautions Toolkit; teach-back resources), Kessels RP (patients’ memory for medical information), Knowles MS (adult learning theory), Miller WR and Rollnick S (Motivational Interviewing), European Health Literacy Survey, Institute for Healthcare Improvement (Always Use Teach-back!).



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