Sundowning: What It Is And How To Deal With It

Sundowning: What It Is And How To Deal With It

Learn about sundowning in Alzheimer's patients and discover strategies to alleviate stress for caregivers in Alzheimer's home care.

When your loved one has Alzheimer’s disease, late afternoon and evening can become some of the most difficult hours of the day. You may feel like the parent you spent time with earlier has suddenly become more anxious, confused, restless, suspicious, irritable, or upset—and you may be exhausted just as their need for reassurance increases.

These changes may be related to sundowning, a pattern of increased confusion, agitation, anxiety, pacing, or other behavioral changes that can occur in the late afternoon and continue into the evening for some people living with Alzheimer’s disease or another dementia. Sundowning is not a separate disease; it is a symptom pattern that can be affected by fatigue, changes in light, overstimulation, disrupted routines, unmet physical needs, or changes in the person’s internal sleep-wake cycle.

For family caregivers, sundowning can feel deeply personal. Your mom may accuse you of keeping her from going home when she is already in her own house. Your dad may repeatedly ask to leave, become angry when you try to redirect him, pace near the door, or resist the bedtime routine that usually goes smoothly. It is understandable to feel frustrated, worried, sad, or unsure what to do next.

The most important thing to remember is that these behaviors are not your loved one’s fault, and they are not a sign that you are failing as a caregiver. Alzheimer’s changes how the brain processes time, surroundings, emotions, and physical discomfort. A consistent routine, a calmer environment, attention to possible triggers, and reliable support can make evenings more manageable for everyone.

Look for Possible Triggers

Sundowning can be more intense when your loved one is hungry, thirsty, tired, uncomfortable, in pain, constipated, needs to use the restroom, is too warm or cold, or is overwhelmed by noise and activity. Because Alzheimer’s can make it harder for someone to recognize or explain what they need, distress may show up as agitation rather than a clear request for help.

Before assuming a behavior is “just sundowning,” take a calm, practical approach. Think through what may have changed in their day or environment.

Consider checking whether your loved one:

  • Has eaten enough food and had enough to drink.
  • Needs to use the restroom or may be experiencing constipation.
  • Is showing signs of pain, discomfort, illness, or medication side effects.
  • Is overtired after a busy day, visitors, errands, or appointments.
  • Has spent too much time in a noisy, crowded, or overstimulating setting.
  • Is confused by dim lighting, shadows, mirrors, television sounds, or unfamiliar surroundings.
  • Has missed their normal meal, activity, medication, or bedtime routine.

Keeping a simple note or journal for a week or two can be helpful. Record when symptoms begin, what happened beforehand, what your loved one ate and drank, their sleep and activity patterns, and which responses seemed to help. This can reveal patterns—such as agitation after late-day television, long afternoon naps, missed snacks, or an overly busy schedule—and give you useful information to share with their healthcare provider.

A sudden or substantial change in behavior should not automatically be attributed to Alzheimer’s. Contact the person’s medical provider if symptoms are new, severe, rapidly worsening, associated with pain or illness, or creating a safety concern. Medical issues, medication changes, poor sleep, infection, dehydration, and other conditions can worsen confusion or agitation.

Bring in Alzheimer’s Home Care

Evening care can be especially difficult because it often arrives at the end of a long day. You may have been working, managing your own household, attending appointments, preparing meals, and responding to your loved one’s needs for hours. When confusion or agitation begins just as your own energy is depleted, it can become harder to remain calm and patient—even when you love your parent deeply.

Alzheimer’s home care can provide meaningful support during these demanding hours. A trained caregiver can offer familiar, steady companionship; help maintain a predictable routine; assist with meals and hydration; provide supervision; and use calm, respectful communication when your loved one becomes distressed.

Rather than trying to reason your parent out of confusion, a caregiver can focus on reassurance, redirection, and comfort. For example, if your mother insists she needs to “go home,” the caregiver may acknowledge the feeling—“You want to be somewhere that feels safe”—and then gently redirect her toward a familiar photo album, a cup of tea, calming music, or another soothing activity. This approach avoids arguing about facts your loved one may no longer be able to process.

Home care can also give families respite during the time of day that may be most emotionally draining. You may use caregiver visits to prepare dinner for your own family, complete errands, take a walk, rest, or simply have a few quiet moments to reset. That support is not a replacement for your role as a daughter, son, spouse, or family member. It can help you preserve your energy so that your time together feels more connected and less consumed by tasks and crisis management.

Create a Predictable Rhythm

People living with Alzheimer’s often feel more secure when the day follows a familiar rhythm. A predictable schedule can reduce the number of decisions your loved one has to make and may reduce the uncertainty that contributes to late-day distress.

Try to keep wake-up time, meals, medications, activities, and bedtime as consistent as possible. The goal is not to create a rigid schedule that causes stress if something changes. Instead, it is to create recognizable patterns that help your loved one know what to expect.

A calming evening routine might include:

  • Turning on lights before the room becomes dim or shadowy.
  • Offering a light snack and a drink.
  • Using the restroom and changing into comfortable clothing.
  • Lowering noise from televisions, phones, household chores, and visitors.
  • Listening to familiar music, looking at family photos, or reading together.
  • Completing a simple, familiar activity such as folding towels or sorting cards.
  • Beginning the bedtime routine at approximately the same time each evening.

Daytime habits matter, too. Exposure to daylight, time outside or by a bright window, safe physical activity, and meaningful activity earlier in the day may support better sleep at night. Try to schedule appointments, bathing, errands, and more demanding activities during the morning or early afternoon, when your loved one may be more alert. Limiting long or late-day naps and avoiding caffeine later in the day may also help protect nighttime sleep.

Make Meals and Hydration Steady

Hunger, thirst, low energy, and fatigue can make anyone more irritable. For a person with Alzheimer’s, those unmet needs may be harder to identify and communicate. By late afternoon, your loved one may not be able to tell you, “I skipped lunch,” “I have a headache,” or “I need something to drink.” Instead, they may appear angry, restless, confused, or resistant.

Consistent mealtimes can help create comfort and reduce avoidable triggers. Offer meals and snacks at approximately the same times each day, and make hydration easy by offering water or other preferred beverages throughout the day—not only when your loved one asks.

A light snack in the late afternoon may be particularly helpful. Consider something familiar and easy to eat, such as fruit, yogurt, cheese and crackers, toast, soup, or another food that fits their dietary needs and preferences. If chewing, swallowing, diabetes, food allergies, or other health conditions are a concern, follow the guidance of their medical team.

You can also make meals less stressful by reducing distractions. Serve food in a well-lit, comfortable setting, limit competing television noise, and avoid presenting too many choices at once. If your loved one becomes overwhelmed by a full plate, smaller portions or simple finger foods may feel more manageable.

Home care providers can help with meal planning, grocery shopping, food preparation, serving meals, cleanup, and gentle encouragement to eat and drink. This can give families peace of mind that daily nutrition and hydration are receiving consistent attention, especially when they cannot be present for every meal.

Lower Evening Stimulation

As daylight fades, shadows, reflections, household noise, fatigue, and unfamiliar activity can all become more confusing for a person with Alzheimer’s. What seems ordinary to you—a television program, the sound of dishes being put away, a mirror in a hallway, or several people talking at once—may feel overwhelming or even threatening to your loved one.

Try to create an evening environment that feels familiar, quiet, and easy to understand.

Helpful adjustments can include:

  • Turn on lights before dusk to limit dark corners and confusing shadows.
  • Use night-lights in the bedroom, hallway, and bathroom for safer overnight orientation.
  • Reduce loud television, news programs, fast-paced shows, phone alerts, and multiple conversations.
  • Keep familiar photos, favorite blankets, comfortable clothing, and meaningful objects nearby.
  • Limit late-day visitors or schedule social activity earlier, if crowds tend to increase agitation.
  • Cover mirrors if reflections appear to confuse or distress your loved one.
  • Keep pathways clear and remove clutter that may increase fall risk during pacing or nighttime waking.

Calming activities can redirect anxious energy without demanding too much concentration. Depending on your parent’s interests and abilities, you might try gentle music from an earlier era, familiar hymns, a favorite movie, looking through photographs, a simple puzzle, folding towels, coloring, reading aloud, or a short supervised walk. Familiar and soothing activities are generally more helpful than asking your loved one to complete a complicated task or explain why they are upset.

Respond With Reassurance

When sundowning leads to anger, accusations, pacing, or repeated questions, it can be tempting to correct your loved one or insist that they remember the facts. But arguing, quizzing them, or repeatedly saying “That’s not true” often increases distress because the confusion feels real to them in that moment.

Instead, focus on the feeling beneath the words. Speak slowly, use a calm tone, offer brief reassurance, and redirect attention when possible.

For example:

  • If your parent says, “I need to go home,” you might say, “You want to feel safe. I’m here with you, and you’re safe.”
  • If they ask repeatedly when dinner is, you might say, “Dinner is taken care of. Let’s have a small snack while we wait.”
  • If they are anxious about a person who is not present, you might say, “You miss them. Let’s look at this photo together.”
  • If they become upset by a task, step back, simplify the environment, and try again later rather than pushing through.

Avoid taking harsh words or accusations personally. Alzheimer’s can change emotional regulation and perception, and the behavior may reflect fear, discomfort, fatigue, or confusion—not your relationship with your loved one. The National Institute on Aging recommends remaining patient, speaking calmly, listening to concerns, avoiding arguments, and reassuring the person that they are safe.

If your loved one becomes physically aggressive or you feel unsafe, prioritize safety. Give them space, avoid restraining them unless immediate safety requires it, remove yourself from the situation if possible, and seek emergency help when there is an immediate risk of harm. Be sure to tell emergency responders that the person has dementia so they can respond appropriately.

You Do Not Have To Manage It Alone

Sundowning can make evenings feel unpredictable, but support and preparation can reduce stress for both your loved one and your family. A thoughtful routine, attention to physical needs, a calmer home environment, and compassionate responses can all help make late-day symptoms more manageable.

If you or an aging loved one is considering Alzheimer’s home care in Bozeman, MT, contact Experience Professional Care Solutions at (406) 551-6700. Their care team can help you explore a personalized plan for companionship, daily routines, meal support, personal care, caregiver respite, and dementia-focused support at home.

Experience Professional Care Solutions provides exceptional home care in Bozeman, Belgrade, Livingston, Three Forks, Manhattan, and surrounding areas.

For additional education and support, families can also explore the dementia and Alzheimer’s resources on the Experience Professional Care Solutions Resources page.

 

Sources for some of our tips:

Facebook
Twitter
LinkedIn
Pinterest
Alzheimer's home care can help establish routines with meals and activities to help reduce sundowning.

Related Posts

We’re now Experience Professional Care Solutions!

Same caring team as Qualicare MT, with a new name and website to better serve you.