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Culturally competent hospice care: a guide for nurses and families
Culturally competent care fits the patient's language, beliefs, food, faith and family, instead of asking the patient to fit the hospice. In nursing it is a skill set: ask, listen, adapt and check back. Federal rules require every hospice to give patients information in a language and manner they understand. This guide covers the standards, the law and the bedside.
Reviewed by our medical director, October 13, 2026

On this page (8 sections)
- What does cultural competence mean in hospice and nursing?
- What does culturally competent care look like at the bedside?
- What are the National CLAS Standards?
- What is the patient's right to information in a language they understand?
- How do interpreter services work in hospice?
- How does an assessment ask about culture and spirituality without assuming?
- For families: how do you tell the team what matters?
- Common questions
What does cultural competence mean in hospice and nursing?
Cultural competence is the ability of a clinician, and the organization behind the clinician, to give care that works for people whose language, beliefs and family life differ from their own. The CLAS Standards call it care that is effective, understandable, respectful and responsive to a person's beliefs, language and health literacy.
Nurse educators pair it with cultural humility: treat each patient as the expert on their own culture, and ask rather than assume. In hospice, pain medicine, feeding, who hears the prognosis and what happens after death are all shaped by culture, and there is little time to get them right.
What does culturally competent care look like at the bedside?
Language
Someone who gets by in English may still want a qualified interpreter for a prognosis or medicine conversation. Offer one before, not after.
Food
A family may bring broth or a traditional dish when the patient eats little. Explain what a fading appetite means without refusing the food, and respect fasting rules.
Religious practice at the bedside
Prayer, scripture, icons, a rosary, a Qur'an or incense may be part of the room. Ask before moving anything, and whether prayer times should shape visits.
Family decision-making
In some families one elder speaks for everyone; in others, decisions are shared. Ask who the patient wants involved, while protecting the patient's own right to decide.
Beliefs about disclosing a prognosis
Some families ask that the patient not be told, believing that naming death hastens it. Do not lie. Ask the patient how much they want to know and who should hear it.
Rituals at the time of death
Washing by family or clergy, a particular position, time undisturbed, or burial within a day may matter. Ask early and tell the funeral home. See signs that death is near.
Gender of the caregiver
A patient may prefer an aide of the same gender for bathing, or want a relative present. Ask at the first visit and plan staffing around it when possible.
What are the National CLAS Standards?
The National Standards for Culturally and Linguistically Appropriate Services in Health and Health Care are 15 standards from the HHS Office of Minority Health. The principal standard asks organizations to provide effective, equitable, understandable and respectful care that responds to diverse cultural health beliefs, preferred languages, health literacy and other communication needs.
The other 14 cover leadership and workforce; communication and language assistance (language help at no charge, qualified interpreters rather than untrained staff or minors, easy-to-understand materials); and engagement and accountability. They are not a law. They describe what the laws below expect in practice.
What is the patient's right to information in a language they understand?
Hospice patient rights (42 CFR 418.52). Before care starts, the hospice must give the patient spoken and written notice of their rights in a language and manner the patient understands. See patient rights.
Title VI of the Civil Rights Act. Every provider paid by Medicare or Medi-Cal must take reasonable steps to give people with limited English proficiency meaningful access.
Section 1557 of the Affordable Care Act (45 CFR 92.201). A qualified interpreter must be provided when needed, at no charge to the patient. A provider may not require a patient to bring an interpreter, or rely on a minor child or an accompanying adult, except in an emergency or at the adult patient's own request after an interpreter is offered. See language assistance.
How do interpreter services work in hospice?
- Step 1
The preferred language is recorded
At the first call or visit, the hospice asks which language the patient and main caregiver prefer for health conversations, and records it.
- Step 2
An interpreter is offered before each important conversation
Consent, the notice of rights, medicine teaching, prognosis and advance care planning all count. A phone or video interpreter can join a home visit.
- Step 3
Family members translate only if the patient asks
Relatives may sit in, but may soften or skip what the nurse says. The patient decides, after being offered a qualified interpreter. The nurse then checks understanding with teach-back.
How does an assessment ask about culture and spirituality without assuming?
Medicare requires the hospice comprehensive assessment (42 CFR 418.54) to cover physical, emotional, psychosocial and spiritual needs. Good assessments use open questions:
- Is there anything about your background, beliefs or traditions we should know as we care for you?
- How much do you want to know about what lies ahead, and who should decide if you cannot?
- Are there foods, prayers, practices or objects that are important to you right now?
- Is there anything that should or should not happen at the time of death and in the hours after?
The answers go into the plan of care so the whole team works from them. The chaplain is offered, never required.
For families: how do you tell the team what matters?
You do not have to wait to be asked. Tell the nurse or social worker at the first visit, or call the office. A hospice nurse answers the phone 24 hours a day, 7 days a week, and can visit when needed.
- Which language you want for medical conversations
- Who speaks for the family, and who should hear news first
- Food, prayer times, fasting, modesty and the gender of the aide
- What should happen at the time of death, including clergy, washing and the funeral home
If something is done wrong, say so. You have the right to voice a grievance without fear of reprisal. Grief support continues for 13 months after a death, and you can tell the bereavement support team what fits your traditions.
Common questions
What is cultural competence in nursing?
Care that fits the patient's language, beliefs, values and family structure. It takes awareness of your own assumptions, knowledge of common differences, the skill to ask, and the habit of adapting care to the answers.
What are examples of culturally competent care?
An interpreter before a prognosis conversation. Asking who the patient wants involved in decisions. An aide of the gender the patient prefers. Respect for fasting rules. Rituals at the time of death planned before they are needed.
How do you provide culturally competent care?
Ask open questions at the first assessment, record the answers in the plan of care, use qualified interpreters, check understanding with teach-back, and ask again as the illness changes.
Why does cultural competence matter in hospice?
The time is short and the decisions are personal. Pain control, feeding, disclosure and what happens after death all carry cultural meaning, and there is rarely a second chance.
What should a nurse do when the family does not want the patient told the prognosis?
Do not argue and do not go around the family. Ask the patient, with an interpreter if needed, how much they want to know and who should receive information. Many patients let a relative handle the details. If the patient wants to know, that right comes first.
About this page
- Written by
- Beta Hospice care team
- Clinically reviewed by
- our medical director
- Last reviewed
- October 13, 2026
- Next review
- April 13, 2027
How we write and review this site
Sources
- HHS Office of Minority Health: National CLAS Standards (opens in a new tab)
- 42 CFR 418.52: Patient's rights (opens in a new tab)
- 42 CFR 418.54: Initial and comprehensive assessment of the patient (opens in a new tab)
- 45 CFR 92.201: Meaningful access for individuals with limited English proficiency (Section 1557) (opens in a new tab)
- HHS Office for Civil Rights: Limited English Proficiency (opens in a new tab)
- National Institute on Aging: What are palliative care and hospice care? (opens in a new tab)
These sources support the general information on this page. For one personās care and coverage, talk with the hospice team.
You do not have to decide alone.
Call (877) 258-7129 any time, or leave your number and someone from Beta's hospice team will call you. No decision is needed to call. Most families start with a question.
Only a hospice doctor, together with the personās own doctor, can confirm hospice eligibility. A website cannot.
- A nurse answers 24 hours a day, 7 days a week
- You can stop hospice at any time
- You have the right to choose your hospice
