Dementia Care Plan Template

A dementia care plan is the plan you make with a patient and their caregiver after a diagnosis of dementia or mild cognitive impairment: test results, stage, function, medicines, behavior, safety, support, and who decides if the patient can’t. Copy the free template, see a new mild Alzheimer’s plan and a moderate mixed dementia plan with evening agitation, and check what goes in each part.

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  • Two filled examples

Blank dementia care plan template

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DEMENTIA CARE PLAN

Patient: [Name, date of birth]
Visit date: [Date]
Visit type: [Cognitive assessment and care planning visit, or plan review]
Present: [Patient, caregiver, other family, interpreter]
History from: [Patient, caregiver or another informant, records, other clinicians]
Clinician: [Name, credentials]

DIAGNOSIS AND COGNITIVE TESTING
Changes noticed: [What the patient and caregiver have noticed, when it started, and how fast it is changing]
Cognitive tests: [Each tool with its score, date, and the patient's years of schooling: MoCA, Mini-Cog, MMSE, or another]
Workup: [Blood tests, brain imaging, hearing and vision checks, mood screen, with results]
Diagnosis: [Mild cognitive impairment or dementia, and the likely cause: Alzheimer's, vascular, Lewy body, frontotemporal, or mixed]
Stage: [Mild, moderate, or severe, and any staging scale used]
How it was shared: [Words used, who was there, the patient's reaction and questions]

FUNCTION
Self-care: [Bathing, dressing, toileting, transfers, continence, eating: on their own, with prompting, or with help]
Household tasks: [Money, medicines, meals, shopping, transport, phone, housework: who does each now]
Mobility and falls: [Walking aid, falls in the past year, injuries]
Hearing and vision: [Aids worn, and checks due]

MEDICATIONS
Reconciled list: [Each medicine and dose, the source checked, and who manages them at home]
Medicines that cloud thinking: [Anticholinergics, sedatives, sleeping pills, opioids: stopped, tapered, or kept, and why]
Dementia medicine: [Cholinesterase inhibitor or memantine: started, continued, changed, or not used, and why]
Dose steps and side effects: [Starting dose, when to raise it, and what to watch for]
Help with medicines: [Blister packs, organizer, reminders, or supervised doses]

BEHAVIOR AND MOOD
Symptoms: [Low mood, anxiety, apathy, agitation, sleep change, hallucinations, delusions, wandering]
Pattern and triggers: [Time of day, how often, what sets it off, what settles it]
Causes checked: [Pain, constipation, infection, hearing loss, medicines, sleep, delirium]
Non-drug plan: [Routine, activity, light and noise, how the caregiver responds]
Medicine for symptoms: [Started or not, the reason, the risks discussed, and the date to review or stop]

SAFETY
Driving: [Driving, stopped, or referred for a driving assessment, and any report the rules where you practice require]
Firearms: [None, locked, or removed, and who holds the key]
Wandering: [Episodes, ID bracelet, door alarm, location device]
Home and cooking: [Stove, fall hazards, living alone, emergency call system]
Money and scams: [Who helps with finances, bank alerts, recent losses]
Abuse or neglect: [Asked, with the patient alone where possible; concerns and action]

CAREGIVER AND SUPPORTS
Main caregiver: [Name, relationship, lives with the patient or not, phone]
Caregiver strain: [Sleep, health, work, mood, and any strain scale score]
Education given: [Topics covered and materials]
Support for the caregiver: [Respite, support group, counseling, their own clinician]
Community services: [Alzheimer's organization, day program, home care, meals, transport: referrals and dates]

ADVANCE CARE PLANNING
Capacity today: [For which decisions, and how you judged it]
Decision-maker: [Name, relationship, and how named]
Legal documents: [Powers of attorney and advance directive: on file, or steps to complete them]
Conversation: [Held today, booked, or recorded in a separate advance care planning note]

OTHER CONDITIONS
Conditions that affect the plan: [Blood pressure, diabetes, heart disease, stroke, sleep, alcohol, weight, continence, pain]
Changes for them: [Targets eased, medicines simplified, tests stopped]

FOLLOW-UP
Next contact: [Phone call or visit, date, and who]
Plan review and retesting: [Date for review and repeat cognitive test]
Call sooner if: [Sudden worse confusion, a fall, side effects, or the caregiver can't cope]
Copies to: [Patient, caregiver, other clinicians, and services]

Signed: [Clinician name, credentials, date]

Use it for

  • After a new diagnosis
  • Mild cognitive impairment
  • Cognitive care planning visits
  • Changes in behavior
  • Day programs and home care

Two filled examples. Every part, filled in.

Each one follows the template. Use them to judge how much detail every part needs.

Dementia care plan: newly diagnosed mild Alzheimer’s dementia

Family practice, cognitive assessment and care planning visit with her husband

Diagnosis and cognitive testing

74-year-old woman, retired bank teller, 14 years of schooling. Her husband first noticed 2 years ago that she repeated questions and forgot recent conversations. In the past 6 months she has missed 2 bills, left the stove on twice, and got lost driving to her sister’s house on a road she has used for decades. She says her memory is “not what it was” but feels she copes. Mini-Cog 2 of 5 at her annual visit 6 weeks ago: 2 of 3 words recalled, clock abnormal. MoCA 19 of 30 today, with most points lost on delayed recall, orientation, and the executive tasks. Blood tests: CBC, electrolytes, calcium, glucose, creatinine, TSH, and B12 normal. MRI: atrophy of both hippocampi, mild small vessel change, no stroke or mass. GDS-15 score 2. Mild hearing loss in both ears on a whisper test. Diagnosis: dementia, most likely due to Alzheimer’s disease, given the slow onset, the memory-first pattern, and the MRI. Stage: mild. Shared with her and her husband using the words dementia and Alzheimer’s. She was tearful, then said it was a relief to have a name for it, and asked first about driving.

Function

Self-care: independent in all 6 areas, Katz ADL 6 of 6. Household tasks: Lawton IADL 5 of 8. Her husband now pays the bills and fills a weekly pill organizer. Since the stove incidents she cooks only when he is home. Still shops with a list, does the laundry and housework, and uses the phone. Walks 30 minutes most days; no falls. Reading glasses; no hearing aids.

Medications

Reconciled with her pharmacy: amlodipine 5 mg daily, atorvastatin 20 mg daily, vitamin D 1,000 units daily, and an over-the-counter night-time pain reliever with diphenhydramine most nights for 3 years, for sleep. Stop the diphenhydramine product: it is anticholinergic and likely adds to her confusion. Plain acetaminophen if she needs it for pain. Sleep plan instead: the same wake time every day, a morning walk outdoors, and no naps after 2 p.m. Start donepezil 5 mg at bedtime; raise to 10 mg after 6 weeks if she tolerates it, at the slower end of the usual range, to limit nausea. Move it to the morning if she has vivid dreams. Pulse 72 and regular; no fainting; not on a beta-blocker. Side effects to watch for: nausea, diarrhea, poor appetite, vivid dreams, muscle cramps, dizziness, or a slow pulse. Benefit expected to be modest: it may keep her thinking and daily function steadier for a time, and doesn’t stop the disease. Memantine not indicated at this stage. Her husband keeps filling the pill organizer.

Behavior and mood

Irritable when she can’t find things, a few times a week; settles when her husband helps without quizzing her. No low mood, with a GDS-15 of 2. No apathy, hallucinations, or wandering. Sleeps about 6 hours. Plan: a wall calendar and a notebook by the phone, keys and glasses in one bowl by the door, and keeping up her garden club and walks. Her husband will give clues rather than test her memory.

Safety

Driving: lost once on a familiar route, and her husband has seen her hesitate at intersections. Referred for a formal on-road driving assessment. She agreed not to drive until the result, and her husband will drive. Checked the reporting rules for the licensing authority where we practice, and followed them. Firearms: her husband’s hunting rifle is in a locked safe with the ammunition stored apart; she doesn’t know the code. Stove: an automatic shut-off device to be fitted this week. Money: her husband added to her bank account, alerts set for large withdrawals, and both warned about phone and email scams. Wandering: none; location sharing turned on in her phone. Abuse: asked alone, she feels safe and well treated.

Caregiver and supports

Husband, 77, retired electrician, lives with her; his own type 2 diabetes is well controlled. Coping well for now, but worried about what is ahead. Education: what to expect in mild dementia, how to help with memory without testing her, and how to spot donepezil side effects. Referred both of them to the local Alzheimer’s organization’s program for people newly diagnosed and their partners, and its early-stage support group. Their daughter lives an hour away and will join the next visit by video.

Advance care planning

Capacity today: she can make her own health care decisions and choose a decision-maker; she explained her choice and her reasons in her own words. She wants her husband to decide for her if she can’t, then her daughter. No powers of attorney or advance directive yet: lawyer appointment for powers of attorney for health care and property within the month. Advance care planning visit booked in 4 weeks with her husband and daughter, to be recorded in its own note.

Other conditions and follow-up

Blood pressure 134/78 on amlodipine: no change. Hearing loss: audiology referral, since treating it may help her follow conversations. Alcohol: 1 glass of wine a week. Nurse phone call in 2 weeks about side effects and sleep. Visit at 6 weeks to raise donepezil, with pulse and weight. Plan review in 6 months; repeat MoCA at 12 months. Call sooner for fainting, a slow pulse, vomiting, weight loss, or a sudden change in confusion. Copies to her, her husband, and the driving assessment center with the referral.

What goes in each part.

Diagnosis and cognitive testing

What led to the plan: the changes noticed, the test scores, the workup, and the diagnosis and stage, with how you shared it.

  • Changes noticed by the patient and an informant, with onset and course
  • Each cognitive test by name, with its score, date, and the years of schooling
  • Blood tests and imaging, and the treatable causes ruled out
  • The diagnosis, its likely cause, and the stage
  • How the diagnosis was shared, and the patient’s reaction

Avoid: A score in place of a diagnosis. Dementia means a decline in daily function as well as on testing, so write down the tasks the patient can no longer manage.

Function

What the patient can still do and what they need help with, so the plan matches the help in place.

  • Self-care: bathing, dressing, toileting, continence, and eating
  • Household tasks: money, medicines, meals, shopping, transport, and who does each now
  • Walking, falls, hearing, and vision
  • A scale such as the Katz ADL or Lawton IADL, if you use one

Avoid: Asking only the patient. People with dementia often rate themselves as more able than they are. Ask the caregiver too, and record both views.

Medications

A full review: medicines that make thinking worse, the dementia medicine decision, and who makes sure the doses are taken.

  • A reconciled list, including over-the-counter sleep aids and allergy pills
  • Anticholinergic and sedating medicines stopped or tapered, with the reason
  • Cholinesterase inhibitor or memantine: the choice, and why
  • The dose steps, side effects to watch for, and the date to review
  • Who manages medicines at home

Avoid: Starting a dementia medicine without clearing out the ones that work against it. Bladder pills such as oxybutynin and sleep aids with diphenhydramine are common culprits.

Behavior and mood

Behavioral and psychological symptoms, the pattern behind them, the causes you checked, and the plan, with non-drug steps first.

  • Each symptom, how often, and at what time of day
  • Triggers and what settles it, from the caregiver’s log or account
  • Pain, constipation, infection, hearing, sleep, and delirium checked
  • Non-drug steps for the caregiver to try
  • Any medicine, its risks, and when to review or stop it

Avoid: An antipsychotic as the first step. In people with dementia they raise the risk of stroke and death; keep them for severe distress or danger, at a low dose, with a date to review.

Safety

The risks that come with dementia, asked about directly, with what was agreed for each one.

  • Driving, and any assessment or report
  • Firearms in the home
  • Wandering or getting lost
  • The stove, falls, and living alone
  • Money, scams, and abuse or neglect

Avoid: Leaving driving and firearms for a later visit. Ask at the diagnosis visit, and write down what the patient and family agreed.

Caregiver and supports

Who provides the care, how they are coping, and the services that help them keep going.

  • The main caregiver’s name, relationship, and phone
  • Their sleep, health, mood, and work
  • The education you gave
  • Respite, day programs, home care, and support groups, with referral dates

Avoid: A plan that names the caregiver but never asks about them. Strain builds slowly; ask at each visit, and act before a crisis.

Advance care planning

Whether the patient can take part in decisions now, who decides when they can’t, and the documents and conversations in place.

  • Capacity today, and for which decisions
  • The decision-maker, and how they were named
  • Powers of attorney and an advance directive: on file, or steps to complete them
  • The conversation held or booked, recorded in its own note

Avoid: Waiting until the patient can no longer take part. In mild dementia most people can still name a decision-maker and say what matters to them.

Other conditions and follow-up

How dementia changes the care of other conditions, and when the plan is looked at again.

  • Conditions that affect thinking or safety, such as hearing loss, blood pressure, or pain
  • Targets eased or medicines simplified
  • The next contact and the plan review date
  • Reasons to call sooner, and who gets a copy

Avoid: Calling a sudden change in confusion the dementia getting worse. A change over hours or days is delirium until proven otherwise.

Common mistakes, and how to avoid them.

A test score as the diagnosis

A MoCA of 19 is a result, not a diagnosis. Dementia needs a decline in daily function too, so record what the patient can no longer do, and who told you.

Missing the medicines that cloud thinking

Bladder pills, older antihistamines in sleep aids, some antidepressants, and sedatives all worsen memory. Ask about over-the-counter products, and stop what you can before adding a dementia medicine.

Treating behavior before looking for a cause

Pain, constipation, infection, a full bladder, and hearing loss all drive agitation. Check them, and try non-drug steps, before any medicine for behavior.

Leaving safety for later

Driving, firearms, the stove, and money are easier to settle at diagnosis than after a crash or a scam. Ask about each, and write down what was agreed.

No caregiver in the plan

The caregiver carries out most of the plan. Name them, ask how they are coping, and arrange respite before strain becomes a crisis.

Talk it through together. Vero writes the plan.

Vero Scribe writes the dementia care plan in your template from the visit, with the patient’s consent, or from your dictation. You review and edit every section, then copy it into your record or export it to Word or PDF. Vero works in 60+ languages.

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Frequently asked questions.

What should a dementia care plan include?

The cognitive test scores and diagnosis, the stage, what the patient can and can’t do, a medication review, behavior and mood, safety including driving and firearms, the caregiver and their support, community services, advance care planning and the decision-maker, other conditions, and follow-up, with copies for the patient and caregiver.

How do you write a dementia care plan?

Start from the assessment: name each test with its score, then the diagnosis and stage. Ask the patient and caregiver about daily tasks, review every medicine, and go through behavior and each safety risk. Name the caregiver and what they need. End with who decides if the patient can’t, the services you referred to, and dates for the next contact and review.

How is a dementia care plan different from a chronic care plan?

A chronic care plan covers several long-term conditions through targets and a flare-up action plan. An advance care planning note records the full conversation about future treatment. A dementia care plan is built around cognition: test scores, function, medicines that affect thinking, behavior, safety, and the caregiver. It names the decision-maker and points to the advance care planning note for the details.

Is there a dedicated visit for cognitive assessment and care planning?

Some health plans and insurers pay for a dedicated cognitive assessment and care planning visit. They usually expect the same parts as this template: a cognitive test, function, stage, a medication review, behavior, safety, the caregiver, advance care planning, and a written plan shared with the patient and caregiver. Check the exact requirements where you practice.

Does mild cognitive impairment need a care plan?

Yes, a shorter one. Record the test scores, the treatable causes checked, such as hearing, mood, sleep, medicines, B12, and thyroid, and the risk factors to work on, such as blood pressure and activity. Cover driving and money if they already cause concern, plan ahead while decisions are easy, and retest in about a year. Cholinesterase inhibitors haven’t been shown to help in MCI; anti-amyloid treatment, where available, needs a specialist assessment.

Is this dementia care plan template free?

Yes. Copy it, or download it as a Word or text file. No account needed.

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