Plantar Heel Pain

About Plantar Heel Pain

  • Plantar heel pain describes pain under the heel, most often near the plantar-medial calcaneus. A typical pattern includes pain with the first steps after rest and pain during or after prolonged standing, walking or running (Koc et al., 2023; Morrissey et al., 2021).
  • Plantar fascia-related heel pain is a clinical presentation rather than a diagnosis established by one test or imaging finding. The terms plantar fasciitis and plantar fasciopathy are also used, but other bone, fat-pad, neural, inflammatory, vascular and referred causes can produce heel pain (Koc et al., 2023; Morrissey et al., 2021).
  • Scope: This pathway supports assessment and nonoperative care for adults with nontraumatic plantar heel pain. It does not cover acute traumatic injury, postoperative care, or serious, systemic, inflammatory, neurological, vascular or referred disease as the primary condition.

About CCG Care Pathways

Purpose

CCG is a knowledge translation resource of the Canadian Chiropractic Association. Its care pathways help chiropractors and other clinicians organize conservative care for musculoskeletal conditions. Each pathway outlines the main steps of the clinical encounter and supports decisions about assessment, care, monitoring, referral, co-management, and discharge. The pathways provide a structured approach to care, not a fixed prescription.

Development

Pathways draw on relevant clinical practice guidelines, systematic reviews, peer-reviewed literature, and safety or professional sources. These sources inform, but do not determine, pathway content. Their findings reflect the questions, populations, outcomes, methods, and judgments used and may not apply to every person. Condition-specific sources are identified by author or organization and year, with full citations in one reference list at the end of the pathway.

Principles of Care

Musculoskeletal conditions are shaped by physical, psychological, social, cultural, and environmental factors, so no single approach fits everyone. Good care is ethical, evidence-informed, person-centred, culturally responsive, and tailored to the patient’s goals, preferences, circumstances, and response. Shared decision-making and informed consent guide care. Education, active rehabilitation, and self-management support recovery, functioning, participation, and long-term health. Regular reassessment shows whether the plan is helping and when to continue, adapt, stop, refer, co-manage, or discharge.populations.

Pathway Flow at a Glance

The pathway follows a recurring clinical cycle: understand the person and their goals; screen for safety and referral needs; develop a working clinical profile; agree on a plan and relevant outcomes; provide care; reassess response and safety; and continue, adapt, stop, refer, co-manage, or discharge as appropriate.

Disclaimer

CCG care pathways support professional clinical judgment; they do not replace it or the advice of a qualified provider. They are not prescriptive, authoritative, or regulatory and are not intended for diagnosis or billing. Clinicians remain responsible for practicing within their competence and scope, meeting applicable legal and regulatory requirements, obtaining informed consent, recognizing emergencies, and arranging referral or co-management when needed.

Plantar Heel Pain Care Pathway

1. Record Keeping

Accurate, timely, and sufficiently detailed documentation supports safe, high-quality care. The record should reflect clinically relevant patient interactions, clinical reasoning, decisions, care provided, and progress over time. Documentation should meet the legal, regulatory, privacy, retention, and organizational requirements that apply where the clinician practices. A structured format, such as SOAP, may support consistency, clarity, and continuity and can be adapted to the encounter and practice setting.

Subjective: Record the patient’s concerns, symptoms, functioning and participation, goals, preferences, relevant history and context, and response or adverse effects from previous care.

Objective: Record relevant examination findings, outcome measures, diagnostic test results when available, and clinically important changes.

Assessment: Record the clinical interpretation of findings, working diagnosis or clinical profile, differential and safety considerations, relevant risk factors or modifiers, and the patient’s progress or response.

Plan: Record care provided or proposed, education and self-management, consent and patient decisions, changes to the plan, agreed outcomes and reassessment point, referrals or co-management, follow-up, and discharge planning.

Document at the time of the encounter or as soon as practicable. Corrections and additions should preserve the integrity of the record. Clear records support patient safety, shared decision-making, communication, continuity, and accountability.

2. Informed Consent
  • Definition: A continuing process in which a capable patient, or an authorized substitute decision-maker when required, voluntarily agrees to a proposed examination or intervention after receiving and understanding the information needed to make an informed choice.
  • Key Aspects:
    • Prior to interaction: Obtain consent before beginning an examination, procedure, or treatment, except where applicable law permits otherwise. Explain what is proposed and why. Revisit consent when the plan or material information changes.
    • Voluntarily and specific: must be voluntary and specific to the proposed care. Consider the patient’s capacity for the decision at the time it is required and follow applicable requirements for substitute decision-making when the patient lacks capacity. The patient may ask questions, refuse, place limits on, or withdraw consent.
    • Transparent process: Use honest, plain, and accessible communication. Offer interpretation or other communication support when needed and consider language, culture, health literacy, disability, and prior trauma. Written or digital information may support but does not replace discussion.
    • Patient understanding and agreement:
      • Diagnosis/prognosis: Explain relevant findings, the clinical impression or working diagnosis, important uncertainty, and the expected course in understandable language.
      • Treatment plan: Discuss the nature and purpose of proposed care, expected benefits, material risks and side effects, burdens, reasonable alternatives, the option of no intervention, and the likely consequences of accepting or declining.
      • Questions: Invite questions, explore goals and preferences, allow appropriate time for a decision, and confirm understanding, for example using teach-back.
    • Documentation: Record the consent discussion and decision, including material information provided, questions, capacity or substitute decision-maker where relevant, consent, refusal, limits or withdrawal, and any need to revisit consent. Follow documentation requirements applicable to the jurisdiction and practice setting.
3. Health History
  • Use culturally safe, trauma- and violence-informed care. Explain why questions matter, seek permission before sensitive topics, and adapt communication to the patient’s language, identity, culture, disability and previous health care experiences (Public Health Agency of Canada, 2018).
  • Patient and contextual information: age; sex and gender when clinically relevant; preferred language and communication needs; work or school; caregiving; footwear needs and access; and the activities, roles and cultural or community connections important to the patient.

Primary concerns

  • Context and onset: side and location; gradual or sudden onset; duration and course; first episode or recurrence; recent change in standing, walking, running, sport, work, footwear or other load; direct impact or injury; and whether symptoms are improving, stable, fluctuating or worsening.
  • Symptom pattern: first-step pain after sleep or rest; pain during or after weight bearing; morning, evening, night or rest pain; severity and irritability; focal or diffuse pain; and response over the next day after activity.
  • Aggravating and relieving factors: standing, walking, running, stairs, hills, barefoot walking, hard surfaces, footwear, stretching, rest, pacing, supports and symptom-relieving strategies.
  • Associated symptoms and participation: swelling, warmth, redness, skin or nail change, wound, bruising, stiffness, burning, tingling, numbness, weakness, calf symptoms or systemic illness; effects on sleep, mobility, self-care, work or school, caregiving, exercise, sport and other valued activities.
  • Body systems review: constitutional and infectious; neurological; cardiovascular and peripheral vascular; respiratory; musculoskeletal and bone health; inflammatory or immune; endocrine or metabolic; skin; haematologic; gastrointestinal and genitourinary; reproductive; sleep; cognition; and mood symptoms that may change safety, the differential diagnosis, care or referral.
  • Health, lifestyle and history: diabetes, neuropathy, vascular disease, inflammatory arthritis, gout, cancer, infection, osteoporosis or other bone-health concerns; previous lower-limb injury, surgery or hospitalization; current medicines and supplements, including corticosteroids and anticoagulants; physical activity, training and occupational standing or walking; footwear; nutrition and low energy availability when relevant; sleep; smoking; alcohol or substance use; and family history relevant to inflammatory, vascular or bone health.
  • Social determinants of health: work demands and control, income, housing, food security, transportation, safety, discrimination, social support and access to suitable footwear, activity options and care when these may shape health or participation (Public Health Agency of Canada, 2026).
  • Previous care and responses: advice, activity changes, stretching, exercise, taping, footwear, heel cups, orthoses, hands-on care, dry needling, shockwave therapy, medicines or injections tried; what helped or did not help; adverse effects; and reasons an approach was difficult to use or continue.
  • Patient perspective: understanding of the problem, priorities, preferences, cultural context, concerns, expectations, confidence with weight bearing and previous experiences of care.
  • Flag review: check Red Flags and refer to the separate fixed Orange Flags and Yellow Flags modules when relevant.

Outcome measures

4. Red Flags: Possible Serious Conditions and Other Causes of Plantar Heel Pain

Red flags are prompts for clinical reasoning, not diagnoses on their own. Interpret the whole presentation, new change and combination of findings, and use clinical judgement.

ACTION: Arrange emergency assessment immediately:

  • Foot or ankle infection with systemic illness: rapidly spreading redness, warmth or swelling; severe or rapidly worsening pain; a wound or drainage; fever or rigors; confusion, faintness or other signs of systemic illness, especially with diabetes, immunosuppression, recent surgery or injection (National Institute for Health and Care Excellence, 2025).
  • Pulmonary embolism: sudden shortness of breath, pleuritic chest pain, haemoptysis, fainting, unexplained tachycardia or low oxygen saturation, with or without leg symptoms (Thrombosis Canada, 2025).
  • Acute limb ischaemia: sudden severe foot or leg pain with pallor or a cold limb, absent or reduced pulses, numbness, tingling or weakness (American College of Cardiology and American Heart Association, 2024).

ACTION: Arrange prompt medical assessment:

  • Local infection, septic arthritis or osteomyelitis: new marked warmth, redness or swelling; severe focal pain; a wound, ulcer or drainage; fever or chills; or infection risk from diabetes, immunosuppression, recent surgery, injection or bloodstream infection. Fever may be absent (American College of Radiology, 2022; Ravn et al., 2023).
  • Deep vein thrombosis: new unilateral calf or leg swelling, pain or tenderness, warmth or colour change without pulmonary symptoms, especially with recent surgery, hospitalization, immobilization, cancer, pregnancy or postpartum status, hormone use or previous venous thromboembolism (Thrombosis Canada, 2025).
  • Calcaneal stress or insufficiency fracture: new focal heel pain and bony tenderness after a rapid load increase or with minor or no trauma, especially with reduced bone strength, prolonged systemic corticosteroid exposure or low energy availability. Reduce impact and weight bearing until assessed (American College of Radiology, 2024).
  • Chronic limb-threatening ischaemia: ischaemic rest pain, a nonhealing foot wound or ulcer, or gangrene (American College of Cardiology and American Heart Association, 2024).
  • Malignancy or bone tumour: previous cancer, unexplained weight loss, bone swelling or an enlarging mass, unexplained fracture, or progressive bone pain that is not linked to movement or is prominent at night (National Institute for Health and Care Excellence, 2026).
  • Inflammatory arthritis or enthesitis: bilateral or multisite heel pain with prolonged morning stiffness, synovitis, several painful or swollen joints, dactylitis, psoriasis, inflammatory bowel disease, uveitis or recent gastrointestinal or genitourinary infection (National Institute for Health and Care Excellence, 2025).

ACTION: Arrange planned referral or shared care when:

  • A neural or referred source may better explain the symptoms: burning, tingling, numbness, weakness, symptoms extending beyond the heel, positive neural findings or lumbar features may need medical, neurological or other regional assessment (Koc et al., 2023).
  • Another heel condition or plantar fascia injury needs clarification: central heel pain, posterior heel pain, a sudden pop or bruising, a palpable defect, marked swelling or a pattern that does not fit plantar fascia-related heel pain may need medical, podiatric or sports-medicine assessment and imaging (Koc et al., 2023).
  • The working diagnosis remains uncertain: coordinate assessment when serious and alternative causes have not been resolved or imaging is likely to change care or referral (American College of Radiology, 2025; Koc et al., 2023).
  • Safety-net advice: seek earlier reassessment for new or worsening redness, warmth, swelling, wound, fever, night or rest pain, inability to bear weight, calf swelling, neurological or vascular change, or rapid loss of functioning. Use emergency care for the findings listed above and document the findings, action, advice and follow-through.
5. Orange Flags: Symptoms of Psychiatric Disorders Requiring Referral

Orange Flags are signs that a mental health or substance use concern may require emergency or timely assessment or shared care, and may change whether and how MSK care proceeds. They are not diagnoses. Ask directly and respectfully when concern arises, considering immediate safety, severity, change from usual, daily functioning and context. Psychosocial factors that may affect recovery but do not require separate mental health or medical assessment are addressed under Yellow Flags.

ACTION: Arrange emergency assessment now when there is immediate danger or an urgent medical need:

  • Suicide, self-harm or harm to others: current intent or plan, a recent attempt, inability to stay safe, or behaviour suggesting an immediate risk of serious harm.
  • Severe change in mental state: extreme agitation, confusion, disorganization, possible psychosis or mania with impaired judgment or unsafe behaviour, or inability to meet basic needs when this creates immediate danger.
  • Substance-related or medical emergency: suspected overdose, severe intoxication, dangerous withdrawal, delirium or another sudden change requiring urgent medical care.

When immediate safety is uncertain, do not leave the person alone while help is arranged. Follow local emergency procedures and call 9-1-1 for immediate danger or urgent medical need. If the person is thinking about suicide, call or text 9-8-8: Suicide Crisis Helpline with them or support them to do so.

If violence, abuse or exploitation is disclosed or suspected, support immediate safety and follow applicable safety and reporting requirements.

ACTION: Arrange prompt medical or mental health assessment when there is:

  • Suicide or self-harm thoughts: thoughts without immediate danger.
  • Substantial symptoms or effects: severe, persistent or worsening symptoms of depression, anxiety, trauma, possible psychosis or mania, eating problems or substance use that substantially affect daily life, decision-making or safe participation in care.
  • Other reasons for assessment: a marked change from usual behaviour or functioning; concern about medication or substance effects; a presentation outside the clinician’s competence; or a request for help.

Agree with the patient on who will be contacted, how soon and what to do if the situation worsens. Confirm that the person has connected with the service when clinically important.

ACTION: Adapt and coordinate MSK care:

  • Safe care: care may continue when it is safe and acceptable and does not delay needed assessment. Adapt communication, examination and care; obtain ongoing consent; and coordinate with other providers with the patient’s permission.
  • Continue the MSK assessment: do not assume that a mental health or substance use concern explains the MSK presentation. Continue to consider physical causes and the patient’s account.
  • Questionnaires: they may support conversation and monitoring, but do not establish a diagnosis or replace direct questions, clinical judgment or action.
  • Acceptable support: ask what type of help is acceptable and whether language, cultural, family, community or other supports are important to the patient.

ACTION: Document and follow up:

Record the concern; relevant questions and the patient’s responses; the safety decision and reasons; actions, advice and referrals; communication and consent; follow-up; and any unresolved concern. Follow applicable privacy, safety and reporting requirements.

For provincial, territorial and national services, see Mental health support: Get help (Public Health Agency of Canada 2026).

6. Yellow Flags: Factors that May Affect Recovery or Participation

Yellow Flags are personal, social, work, school, healthcare, environmental or structural factors that may influence symptoms, functioning, participation or response to care. They are contextual, not diagnoses or certain predictions, and do not mean that symptoms are psychological. They guide how care is tailored and do not by themselves require urgent referral. Explore them through conversation and ongoing outcome review, with attention to the patient’s priorities, strengths and circumstances. A separate Yellow Flag score is not required. New or worsening signs of serious physical illness follow the Red Flag process. Mental health or substance use concerns that need separate assessment, or any immediate safety concern, follow the Orange Flag process and applicable emergency or safeguarding procedures.

Explore relevant factors:

  • Understanding, expectations and healthcare experiences: concerns about injury or damage, uncertainty, recovery expectations, confidence, conflicting advice, previous dismissal or harm, and trust in care.
  • Responses to symptoms and activity: worry, fear, avoidance, cycles of doing too much and then needing prolonged rest, difficulty pacing, coping, sleep, confidence in self-management, and return to meaningful activities.
  • Emotional and life context: distress, low mood, anxiety, grief, trauma, caregiving, relationship change, job loss or other major events. Ask permission before sensitive questions and limit discussion to what is relevant and acceptable to the patient.
  • Relationships, culture and strengths: supportive relationships, isolation, family and community roles, cultural or spiritual practices, identity, preferences, language and other sources of resilience.
  • Work, school and administrative context: physical and psychosocial demands, control, satisfaction, job security, accommodations, return concerns, and compensation, insurance or legal processes. Explore these neutrally and in context.
  • Social and structural conditions: consider social and structural determinants of health (Public Health Agency of Canada 2026), including income, housing, food security, transportation, childcare, access and cost of care, discrimination, racism, colonialism, neighbourhood and workplace conditions, and physical or digital accessibility.

ACTION: Respond with the patient:

  • Ask, do not assume: use open questions to understand what helps, what gets in the way, what matters and what feels feasible. Ask about strengths and protective factors, not only difficulties. Do not treat a person’s circumstances, culture or choices as a deficit.
  • Plan together: integrate relevant findings into shared goals, education, self-management, physical activity or exercise, and participation in meaningful activities. Adapt communication, setting, pace, cost and access where possible.
  • Connect and coordinate: with the patient’s consent, consider appropriate clinical, social, workplace, school, community, Indigenous or culturally specific supports. Clarify who will do what and follow up when the connection is important to the plan.
  • Review response to care: reassess the patient’s account and the pathway’s selected outcomes at clinically relevant points. If progress differs from expected, review the clinical impression, care plan, access and other barriers; do not automatically attribute the outcome to Yellow Flags.
  • Document: record relevant factors and strengths, the patient’s priorities and preferences, agreed actions, consent, referrals or coordination, follow-up, and any change requiring the Orange Flag process.
7. Physical Examination

Select examination elements that answer a clinical question or may change care. Adapt the examination to the patient’s presentation, comfort, consent and abilities.

  • Consent and comfort: explain what you propose, provide choices about positioning, draping, pace and support, and confirm ongoing consent.
  • Condition-specific safety: defer provocative testing and arrange appropriate assessment when infection, vascular disease, fracture, tumour or another serious condition is suspected.
  • Observation and gait: weight-bearing tolerance, gait, heel contact, stance time, foot posture, swelling, skin and nail changes, muscle bulk, guarding, asymmetry, footwear and use of supports.
  • Location and palpation: map the painful area and compare sides; examine the plantar-medial calcaneal tubercle and plantar fascia, central heel pad, calcaneus, Achilles insertion and nearby structures when this helps distinguish a presentation.
  • Movement and range of motion: ankle dorsiflexion in weight bearing and non-weight bearing as relevant, plantarflexion, first metatarsophalangeal extension and foot or ankle movement that may change the working diagnosis or plan.
  • Strength and load tolerance: plantarflexor and foot-muscle strength, endurance and control; note familiar pain and response during and after heel raises or another graded loading task.
  • Plantar fascia-related pattern: familiar plantar-medial heel pain with first-step loading, palpation near the medial calcaneal tubercle or passive great-toe extension supports the presentation after competing causes have been assessed. No single finding is diagnostic on its own (Koc et al., 2023; Morrissey et al., 2021).
  • Functional assessment: select safe tasks linked to the person’s goals, such as standing, walking, stairs, squat, heel raise, running, jumping or work- and sport-specific activity. Note symptoms, movement strategy, confidence, capacity and next-day response.
  • Neurological and vascular examination, when indicated: lower-limb strength, sensation, reflexes and neural provocation; pulses, skin temperature, colour, capillary refill, swelling and other tests guided by the presentation.
  • Regional and differential examination: examine the ankle, Achilles tendon, foot joints, lumbar region, peripheral nerves or other areas when the history suggests another or overlapping source.
  • Imaging: not routine for a typical plantar fascia-related presentation. It can investigate fracture, infection, tumour, plantar fascia tear, neural entrapment or another suspected cause when the result is likely to change care or referral (American College of Radiology, 2025; Koc et al., 2023).
  • Repeat and adapt the examination when needed to review progress, revisit the working diagnosis or decide whether further assessment or referral is appropriate.
8. Clinical Presentations

Working clinical presentations

Presentations can overlap or change. Use the history and examination, and imaging when it will change care. Do not infer a tissue diagnosis from pain location, one provocative test or an imaging finding alone (Koc et al., 2023).

  • Plantar fascia-related heel pain: plantar-medial heel pain that is most noticeable with the first steps after sleep or rest and may increase during or after prolonged standing, walking or running, with familiar tenderness near the medial calcaneal tubercle (Koc et al., 2023; Morrissey et al., 2021).
  • Calcaneal fat-pad pain: pain is centred under the heel and is often aggravated by barefoot walking, hard surfaces or prolonged standing, with central heel-pad tenderness rather than focal plantar-medial tenderness. Diagnostic criteria are not well established; reassess for fracture or another cause when pain is focal, severe or load-related (Chang et al., 2022).
  • Neural or referred heel pain: burning, tingling, numbness, night symptoms or pain extending beyond the heel may reflect peripheral nerve involvement or lumbar referral. Objective neurological findings or progression change the need for referral (Koc et al., 2023).
  • Plantar heel pain without a confirmed specific presentation: symptoms appear musculoskeletal after serious, inflammatory, vascular, neurological and referred causes have been assessed, but the available findings do not support a more specific pattern. Record the working impression and revisit it as the course and response to care become clearer.
9. Treatment Considerations

Develop care with the patient. Choices reflect the working presentation, safety, goals, preferences, culture, access, other health conditions, previous responses and the burden of care. Respect the patient’s right to accept, decline, limit or stop any part of care.

Treatment evidence: the intervention evidence below applies to plantar fascia-related heel pain. It does not establish the same treatment for calcaneal fat-pad pain, neural or referred heel pain, or a presentation that remains unclear (Koc et al., 2023; Chang et al., 2022).

Education, self-management, and participation

  • Explanation and shared understanding: explain the working presentation, what the examination shows, why imaging is often unnecessary and how heel symptoms can respond to changes in load and tissue capacity without implying that pain always means damage (Koc et al., 2023; Morrissey et al., 2021).
  • Activity and load: identify recent or sustained standing, walking, running, jumping or work demands linked to symptoms. Options include temporary changes to volume, frequency, intensity, surface or recovery, followed by gradual exposure toward meaningful activity (Koc et al., 2023; Morrissey et al., 2021).
  • Footwear and daily self-management: comfortable footwear, pacing, planned breaks and symptom-relieving strategies can be matched to the person’s activities, work requirements, access and response (Koc et al., 2023; Morrissey et al., 2021).
  • Participation: task changes, temporary work or school accommodations and communication with employers, coaches or teams can help maintain valued roles while standing and walking capacity is rebuilt.

Physical activity and exercise

  • Plantar fascia and calf stretching: plantar fascia-specific stretching and gastrocnemius or soleus stretching can form part of care. The type, frequency and intensity reflect irritability, goals and response (Koc et al., 2023; Morrissey et al., 2021).
  • Foot and ankle strengthening: progressive resistance exercise for the plantarflexors and other foot and ankle muscles can be used to build capacity for walking, standing, running or other goals (Koc et al., 2023).
  • Conditioning and return to activity: aerobic activity, walking or running progression and task-specific exercise can be adjusted to current capacity and advanced using symptoms, next-day response and repeated outcomes.

Hands-on and symptom-relieving care

  • Taping: rigid or elastic foot taping can be tried with other care for short-term symptom relief or to make a meaningful task easier (Koc et al., 2023; Morrissey et al., 2021).
  • Foot orthoses: prefabricated or custom orthoses can be combined with education and exercise when the person’s response indicates a useful fit. Continued use reflects benefit, tolerance, footwear and cost (Koc et al., 2023; Morrissey et al., 2021).
  • Night splints: a one- to three-month trial can be used when first-step morning pain remains a prominent concern and the person can tolerate the device (Koc et al., 2023).
  • Manual therapy and soft-tissue techniques: joint or soft-tissue care to the foot, ankle or calf can be used when relevant restrictions or symptoms limit activity. Review whether it makes active care or a meaningful task easier (Koc et al., 2023).
  • Dry needling: dry needling of relevant calf or foot trigger points can be used as an adjunct within the clinician’s scope, with response and adverse effects reviewed (Koc et al., 2023).
  • Low-level laser therapy: can be used as an adjunct for short-term pain relief in plantar fascia-related heel pain (Koc et al., 2023).
  • Extracorporeal shockwave therapy: shockwave therapy can form part of shared care for persistent plantar fascia-related symptoms when the diagnosis has been reviewed and expected benefits, discomfort, cost and availability have been discussed (Babatunde et al., 2019; Morrissey et al., 2021).

Care for other working presentations

  • Calcaneal fat-pad pain: evidence for specific nonoperative treatment is sparse. Options include temporarily reducing impact and hard-surface exposure and trying heel cushioning or taping; continuation depends on observed response (Chang et al., 2022).
  • Neural or referred heel pain: treatment follows the suspected peripheral nerve, lumbar or other source rather than a plantar fascia protocol. Repeat neurological findings when symptoms change, and use the relevant pathway or arrange referral or shared care when needed (Koc et al., 2023).
  • Plantar heel pain without a confirmed specific presentation: base care on the predominant findings and response, and revisit the differential diagnosis before using options supported only for plantar fascia-related heel pain.

Psychological, social and interdisciplinary support

  • Persistent pain or movement concern: psychologically informed education, graded exposure and support for confidence can be integrated when fear, distress or uncertainty is limiting activity or participation.
  • Coordinated support: communication with primary care, podiatry, physiotherapy, sports medicine, workplace, coaching, dietetic, vascular or mental health services can address needs outside one clinician’s scope, including bone-health concerns, diabetes, inflammatory disease or barriers to participation.
  • Cultural and community supports: traditional or Indigenous healing approaches, spiritual practices and community supports identified by the patient can be included when they fit the person’s goals and are coordinated safely with other care.

Medication and procedural shared care

  • Medication and injection questions: coordination with primary care, pharmacy, podiatry or another authorized clinician can address potential benefits, harms, contraindications and interactions in the context of the working diagnosis and current medicines.
  • Specialist assessment: medical, podiatric or surgical assessment can be coordinated when symptoms remain severely limiting despite an adapted plan, the diagnosis needs review or procedural options are being discussed.

Monitoring and reassessment

  • Agree on a reassessment point based on the presentation, safety, goals, care being tried, patient needs and access rather than a fixed visit schedule.
  • Repeat the baseline outcome set and review first-step and weight-bearing symptoms, functioning, participation, benefits, harms and goals. When a neural or referred presentation is suspected or symptoms change, repeat lower-limb motor, sensory, reflex and neural provocation findings.
  • Continue, adapt or stop care according to response. Revisit Red Flags, the working presentation, differential diagnosis, imaging, referral or shared care when progress differs from expectations or new safety concerns emerge.
10. Prognosis and Prognostic Factors
  • Expected course: the course varies by person. Plantar fascia-related heel pain can improve, persist, fluctuate or recur, and no universal recovery timeline applies. The course of calcaneal fat-pad pain and neural or referred heel pain is not established by plantar fascia studies (Gulle et al., 2023; Chang et al., 2022).
  • Factors associated with a less favourable course: evidence is limited and mostly low quality. Female sex and bilateral heel pain were associated with a less favourable long-term outcome in one cohort. Other reported factors predicted response to particular treatments rather than the overall course; no factor reliably predicts an individual’s recovery (Gulle et al., 2023).
  • Potential supports for recovery: a clear explanation, feasible load changes, progressive exercise, comfortable footwear or supports, confidence with weight bearing, suitable workplace accommodations, access to care and timely shared care may support functioning and participation.
  • Discussing prognosis: describe uncertainty in plain language, ask what the patient wants to know, and update the outlook using goals, repeated outcomes and the observed response over time. Do not use one test, imaging finding or prognostic factor as a fixed prediction.
11. Ongoing Follow-up

Ongoing follow-up is a shared review of whether the plan remains safe, useful, acceptable and aligned with the patient’s goals. The timing of review should reflect symptoms, risk, the care being tried, goals and access rather than a fixed visit schedule.

  • Review symptoms and safety: ask what has changed in symptoms, functioning and daily activities; review adverse effects; and check for new or worsening Red Flags and relevant Orange or Yellow Flag concerns. Arrange earlier or urgent assessment when the findings require it.
  • Review outcomes: repeat the small set chosen at baseline and use the same measures when possible. These may include the Patient-Specific Functional Scale, WHODAS 2.0, quality of life using the patient’s own rating or a measure such as WHOQOL-BREF, symptom impact, participation and the patient’s own assessment of change. Interpret measures with the patient and alongside what has changed in daily life rather than relying on a score alone.
  • Review goals, preferences and consent: ask whether care remains acceptable, feasible and worthwhile; revisit goals and priorities; and confirm consent when the plan or circumstances change.
  • Adapt care: continue what is useful and acceptable, and change, pause or stop what is not. If progress is not sufficient from the patient’s perspective, review the clinical impression, the fit and amount of care, barriers to participation, other health or social factors and whether other expertise is needed.
  • Support self-management and participation: review the strategies the patient is using, including physical activity or exercise, symptom management, pacing and participation in work, school, caregiving, recreation or community life. Ask what is helping and which barriers can be addressed.
  • Referral and co-management: arrange emergency assessment for Red Flags requiring urgent care. Consider referral or co-management when findings or needs are beyond the clinician’s role, the patient’s condition is worsening, progress remains insufficient after the plan has been reviewed, or the patient requests another opinion.
  • Plan the next step: agree whether to continue, change the interval between visits, move toward more self-directed care, or apply the Criteria for Discharge section.
12. Criteria for Discharge

Discharge is a shared decision about ending or transferring a course of care. It does not require complete symptom resolution, a normal outcome score or a fixed number of visits.

  • When discharge may be appropriate: consider discharge when the patient’s goals have been met to a degree they consider satisfactory; the patient feels able to manage with less or no clinician involvement; the patient chooses to end care; continued care is not providing enough benefit to justify its burden, cost or time; or care is being transferred to another provider.
  • Reassess before discharge: review symptoms, functioning, participation, selected outcomes, goals, adverse effects, confidence and preferences. Check for new or worsening Red Flags and any Orange or Yellow Flag concerns that still require action. If the condition is worsening or a safety concern remains, arrange the required assessment or referral rather than routine discharge.
  • When progress has slowed: review the clinical impression, response to care, goals, barriers and access, other health or social factors, and other reasonable options before deciding with the patient whether to continue, change or end care.
  • Plan after discharge: agree on self-management, physical activity or exercise, symptom management, pacing and participation in work, school, caregiving, recreation or community life. Explain which changes should prompt earlier or urgent assessment and when and where to seek care.
  • Future access to care: explain how the patient can return if symptoms recur, functioning declines, or goals or demands change. Any planned future review or supportive care should have an agreed purpose, expected benefit and review point.
  • Referral or transfer: explain the reason, share a relevant summary with the patient’s consent, and clarify who will address outstanding concerns when possible. Avoid an unintended gap in care when safety or ongoing needs remain.
  • If the patient ends care or does not return: respect the patient’s right to stop. Record what is known and unknown about the outcome, advice or referral offered, attempts to communicate when clinically warranted, and any unresolved safety concern. Follow applicable record keeping and communication requirements.
  • Documentation: record the reason care ended, the patient’s status and selected outcomes, goals and preferences, unresolved concerns, advice and self-management plan, referral or transfer details, and how to seek care again if needed.

References and Resources

Disclosure: Generative artificial intelligence tools assisted with drafting, editing, and reference organization. They did not approve the pathway or replace clinical judgment. CCG reviewers verified all content.