Health Literacy: The First Step to Empowered Self-Management


Health literacy, defined as the degree to which individuals can obtain, process, and understand basic health information and services needed to make appropriate health decisions, has become an important concept in healthcare over the past few decades. However, the current approach to health literacy focuses too heavily on functionally evaluating a patient's reading, writing, and numeracy skills. This overly simplistic view of health literacy fails to account for the complex sociocultural factors that affect a patient's ability to truly understand their health and make empowered healthcare choices.

The traditional health literacy model views poor health literacy as an individual deficit that needs to be "fixed" through education and simplified messaging. But this perspective ignores the roles that poor communication, confusing healthcare systems, and power imbalancesplay in hindering patients' capacities to manage their health. Rather than putting the onus entirely on patients to improve their literacy, the healthcare system itself needs to evolve to better empower diverse patients and meet their needs.

Socioecological Model Provides Wider Lens

Experts in health literacy and patient empowerment have called for the adoption of a socioecological model to understand the multidimensional influences on patients' capacities to obtain, process, and apply health information. This model considers health literacy as the product of intersections between individual skills and the social, cultural, political, and environmental contexts in which healthcare communication occurs.

From this viewpoint, health literacy emergence from dynamic interactions between patients and their surroundings. Improving literacy and empowerment requires going beyond functional skills to address wider systemic inequities, limited health knowledge access, cultural mismatchwith providers, and imbalanced power differentials that disempower marginalized patients.

Failure to Recognize Sociocultural Dimension

The current prevalent view of health literacy as an individual competencehas concerning implications. First, it puts the onus entirely on patients to improve their literacy through education. But gaining functional skills without addressing external barriers provides limited benefits. Patients with strong literacy skills can still be disempowered by unclear communication, confusing healthcare systems, lack of transparency, and dismissive attitudes from providers.

Second, the individual deficit perspective stigmatizes patients with poor literacy as ignorant, lazy, or unintelligent. This deficit labeling measures patients against white, educated, middle-class norms without acknowledging how societal inequities influence literacy. Framing health literacy as an individual responsibility shames already marginalized groups instead of recognizing external factors that hamper their healthcare engagement.

Finally, an individual focus overlooks how cultural backgrounds shape patients' health beliefs, communication preferences, and behaviors. Culture powerfully influences how people conceive of health and illness, what treatments they trust, their communications styles, their values around healthcare, and their willingness to question providers. Ignoring sociocultural differences alienates diverse patients from fully engaging in care.

How Systemic Factors Disempower Patients

Health literacy interventions that simply provide functional education miss the mark because they do not address systemic factors that disempower patients, even those with strong literacy skills. These disempowering forces include:


  • Health system complexity - Fragmented systems with little care coordination or transparency confuse patients and hinder their ability to navigate care.
  • Poor communication - Complex medical jargon, vague explanations, rushed consultations, and dismissive attitudes impede understanding.
  • Power differentials - Traditional physician paternalism, intimidating hierarchies, and marginalizing behaviors inhibit patients from meaningful involvement.
  • Inequitable access - Disadvantaged patients face greater barriers finding trustworthy information, getting to appointments, covering costs, and asserting their needs.
  • Cultural mismatch - White, Western biomedical values engrained in healthcare marginalize diverse cultural norms around health, illness, and communication.
  • Biased assumptions - Providers often unconsciously stereotype patients based on socioeconomic status, race, gender and make erroneous assumptions about their capacities.


All of these institutional forces undermine patients' capacities to obtain, process, understand, and apply health information. Without addressing them, health literacy initiatives will fail to truly empower patients as partners in their healthcare.

Toward True Patient Empowerment

Improving functional health literacy skills is important but insufficient for meaningful patient empowerment. The following systemic changes are also needed:


  • Simplify healthcare systems and enhance navigation aids to decrease confusion and fragmentation. Provide coordination across settings.
  • Prioritize clear communication and confirm comprehension by using teach-back. Welcome questions. Avoid jargon and condescending attitudes.
  • Share power through informed, shared decision-making. Validate patient expertise about their own lives and needs.
  • Increase access to reliable online health information through trusted portals and virtual coaches.
  • Provide professional interpreters and translated materials for non-English speakers.
  • Cultivate cultural humility among providers. Train them to understand sociocultural influences on health beliefs and behaviors.
  • Explore new models of care like community health workers and patient navigators to provide culturally attuned support.
  • Partner with communities to co-design programs. Engage patients as advisors in developing services that match their needs and preferences.
  • Advocate for policies to improve literacy accessibility and reduce systemic inequities impeding marginalized groups.


A narrow view of health literacy as an individual competence will not suffice to meaningfully empower patients. A socioecological lens illuminates the external barriers that disempower patients with both high and low functional literacy. Only by addressing system-level forces that shape health literacy emergence and embodiment will healthcare finally empower diverse patients as true partners. This requires moving beyond functional skills to re-envision healthcare systems, communication practices, and cultural perspectives.

While systemic changes are critical, improving health literacy and empowerment also relies partly on patients embracing greater self-management and personal responsibility. Patients who proactively educate themselves, ask questions, manage chronic conditions, and organize care across providers have better health outcomes.

However, the ability to self-manage requires health literacy skills and self-efficacy. Poor literacy and lack of confidence hamper patients' capacity to take ownership of health behaviors, track symptoms, coordinate care, and voice needs. Some ways to boost self-management include:


  • Health coaching and support groups to motivate behavior change and teach self-care skills. This promotes self-efficacy.
  • Plain language education materials and clear instructions for treatment plans allow patients to better adhere to regimens.
  • Tools like online patient portals and symptom trackers. This facilitates monitoring health data and involvement.
  • Reminder systems for appointments, immunizations, and medications. These tools compensate for literacy issues impeding self-management.
  • Shared decision making and motivational interviewing to empower patients to voice preferences and set health goals.
  • Directly addressing psychological and social barriers like low health self-efficacy, competing life demands, and cultural norms that may inhibit self-management.
  • Advanced care planning conversations to clarify patients' values, goals, and preferences for future treatment. This facilitates autonomy and personalized care.


While systemic change is crucial, improving individual self-management capacity through education, tools, and motivational support enables patients to take greater ownership of health behaviors. This dual approach targeting both healthcare systems and individual patients provides a multidimensional strategy to boost health literacy and empowerment. However, the onus should not fall entirely on patients. Providers and healthcare organizations must partner to fix disempowering systemic and communication barriers while supporting self-management capacity.


The relationship between health literacy and patient empowerment is complex, shaped by individual skills, sociocultural factors, and systemic barriers. While increasing functional literacy is important, empowerment crucially depends on re-envisioning healthcare delivery to dismantle disempowering forces. This requires simplifying systems, improving access, embracing cultural humility, and rectifying power imbalances.

There are reasons to be optimistic about progress. Innovative models like patient schools offer promising ways to simultaneously boost health literacy and empowerment. As pioneered by nursing scholar Roi Shternin, patient schools deliver disease-specific education to build self-efficacy and self-management skills. Combining plain language teaching with peer support and shared medical decision-making, these programs provide multidimensional literacy and empowerment benefits. Early research shows improved clinical outcomes, knowledge, patient activation, and satisfaction.

Moving forward, health literacy and empowerment initiatives must take an ecological view addressing both individual and systemic factors holistically. With thoughtful policies, committed providers, and patient partnerships, a healthcare revolution is possible. We can collectively re-engineer care delivery to foster informed, empowered patients fully equipped to manage health within supportive systems. The result will be equitable care where all patients can obtain services, understand options, and have their voices heard. The future is bright for transforming healthcare to truly embody patient-centered care ideals.


Further reading:

  1. Low Health Literacy and Health Outcomes: An Updated Systematic Review ↗
  2. The Implications of Health Literacy on Patient–Provider Communication ↗
  3. Impact of Patient Education on Chronic Disease Self-Management ↗
  4. Digital Health Interventions: Can They Help in Improving Health Literacy? ↗
  5. Peer Support in Health Care and Prevention: Cultural, Organizational, and Dissemination Issues ↗
  6. Educating Family Caregivers for Older Adults About Delirium: A Systematic Review ↗
  7. Incorporating Health Literacy in Education for Socially Responsible Physicians ↗
  8. The Role of Health Literacy in Health Outcomes and Health Disparities ↗
  9. Behavior Modification Techniques in the Management of Chronic Health Conditions ↗