Agitation in Alzheimer's Clinical Trials

Advancing Neurology Research

Caring for Someone with Alzheimer's Disease and Agitation?

Clinical Trials May Help Explore Potential Treatment Options

Agitation is one of the most common neuropsychiatric symptoms of Alzheimer’s disease. It is generally described as emotional distress accompanied by excessive motor activity, verbal outbursts, or aggressive behavior that is not explained by another medical or psychiatric condition. Reported estimates suggest agitation affects a substantial share of people living with Alzheimer’s dementia at some point in the course of the disease.

Agitation can appear at any stage but is often more frequent and more severe as the disease progresses. It may show up as pacing, restlessness, repeated questioning, resistance to personal care, verbal outbursts, or physical aggression. These symptoms can disrupt daily routines, increase safety risks at home, and add significant strain for family members and caregivers.

If you are caring for an adult with Alzheimer’s disease who experiences agitation, Revival Research Institute is conducting Agitation in Alzheimer’s Clinical Trials to evaluate an investigational treatment approach for adults living with this condition.

Are You Eligible to Participate?

To qualify for the Agitation in Alzheimer’s Clinical Trials, participants must:

*Additional criteria may apply.

Participation is free of cost. To learn more or determine whether your loved one may qualify, complete the form below. A member of our research team will contact you to discuss potential eligibility.

This field is for validation purposes and should be left unchanged.
Who is this information for?*(Required)

Please provide YOUR contact information only.

Name(Required)
Best Time to Call(Required)
User Agreement(Required)
This is our Privacy Policy.

Agitation in Alzheimer's Clinical Trials Flyer

About Agitation in Alzheimer's Clinical Trials

Managing agitation in Alzheimer’s disease often requires a combination of caregiver strategies, environmental adjustments, and ongoing medical supervision. Because symptoms can change in frequency and intensity over time, families frequently look for additional options beyond what is currently available.

Revival Research Institute is conducting Alzheimer’s with Agitation Research Studies in Texas for adults with a clinical diagnosis of Alzheimer’s disease who experience agitation. The study is designed to evaluate the safety and efficacy of an investigational treatment being studied for agitation associated with Alzheimer’s dementia.

*All study-related procedures and study treatments are provided at no cost to eligible participants. No insurance is required to participate.

*To take the next step, submit the form above, and our research staff will contact you to determine if your loved one qualifies. A brief discussion about their health and medical history may be required.

Get Started
What to Expect?

If you are caring for an adult with Alzheimer’s disease and agitation, they may qualify for Agitation in Alzheimer’s Clinical Trials exploring potential treatment options. After completing the interest form above, a member of our research team will contact you for a brief pre-screening discussion to determine whether the initial eligibility requirements are met.

If the participant qualifies, an Informed Consent Form (ICF) will be reviewed and signed. This document explains the study procedures, potential risks, possible benefits, and participant responsibilities before any decision to participate is made. Depending on the participant’s capacity to consent, a legally authorized representative may need to provide consent, with the participant’s assent, in line with the study protocol and applicable regulations.

Once consent is provided, the participant may be invited to one of Revival Research Institute’s study sites for additional screening evaluations. These assessments may include a physical examination, review of medical history, vital signs, laboratory testing, cognitive and behavioral assessments, and other evaluations required by the study protocol.

Participants who meet all study requirements may be enrolled in the study. Our team will make sure you and your loved one fully understand what participation involves and what to expect throughout the study duration. You are encouraged to ask questions at any time.

Age Icon
Age
≥55 to 90 years old
Condition Icon
Condition
Agitation Associated with Alzheimer’s Disease
Location Icon
Location
Texas

Agitation in Alzheimer's Disease
A Common Neuropsychiatric Symptom

Alzheimer’s disease is a progressive neurodegenerative condition that affects memory, thinking, and behavior. Alongside cognitive decline, many people with Alzheimer’s develop neuropsychiatric symptoms, and agitation is among the most frequently reported. It is assessed clinically using caregiver-reported tools and structured behavioral scales rather than a single laboratory test.

Agitation in Alzheimer's May Present Through:

Common Features Associated with Agitation in Alzheimer's Disease Include:

The presentation and severity of agitation can vary depending on the stage of Alzheimer’s disease, the individual’s environment, and other contributing medical factors.

Frequently Asked Questions

Your Guide to Agitation in Alzheimer's Disease

Got questions about agitation in Alzheimer’s disease? You’re not alone.

We’ve compiled answers to some of the most common questions about agitation in Alzheimer’s, including its causes, symptoms, assessment, treatment, and clinical trial participation. Still have questions? Contact our research team for more information. Call us at +1 (248) 721-9539, we’ll be happy to assist you.

Agitation is a neuropsychiatric symptom of Alzheimer's dementia. It is generally described as emotional distress along with excessive motor activity, verbal outbursts, or aggressive behavior that causes distress or interferes with daily functioning and is not better explained by another condition.

Agitation is linked to the underlying changes Alzheimer's disease causes in the brain, and it can be triggered or worsened by other factors: pain, infection, medication side effects, poor sleep, overstimulation, unfamiliar surroundings, or difficulty communicating a need.

Assessment usually combines a clinical evaluation with caregiver-reported information about behavior. Clinicians may use structured tools such as the Cohen-Mansfield Agitation Inventory (CMAI) or the Neuropsychiatric Inventory (NPI), along with a medical review to rule out other causes such as pain or infection.

Management is individualized. Non-drug approaches are typically tried first and may include adjusting the environment, establishing consistent routines, and caregiver-focused strategies. In some cases a physician may also consider medication, with ongoing monitoring. Treatment decisions should always be made with a qualified healthcare provider.

In many cases, yes. When a participant is unable to provide informed consent independently, a legally authorized representative may provide consent on their behalf, with the participant's assent, as permitted by the study protocol and applicable regulations. Most agitation studies also require a caregiver or study partner who can attend visits and report on symptoms.