Participate in a Study

Currently, more than 6 million Americans have Alzheimer’s disease, the most common form of dementia. By 2050, that number is projected to triple. Though so many are affected, challenges in finding volunteers hinder our efforts at developing a cure. As a research volunteer, you champion the effort to prevent, slow, and, one day, cure Alzheimer’s disease and related dementias

Participation in research is the only way we can hope to find cures for diseases such as Alzheimer's disease and promote normal healthy brain aging for all.

We have a variety of studies for individuals with and without memory loss. To discuss how you can participate please call us at (859) 323-5550. Alternatively, you can give us some basic information by completing our online research interest form and we will get back in touch with you soon. Click here to access the research interest form.

 

Featured Studies

University of Kentucky Alzheimer’s Disease Center Brain Aging Research Study

The UK- Center brain aging research program is our longest-running research study for individuals with and without memory problems. This is a unique opportunity to contribute to ongoing research in the areas of Alzheimer's disease and normal aging. Read Brain Aging Flyer Here.

SMArT-HS Study
One in five persons diagnosed with Alzheimer's disease actually have LATE  (Limbic associated TDP-42 encephalopathy), formerly known as Hippocampal Sclerosis of Aging. SMArT-HS is a phase IIa study to assess the safety and tolerability of nicorandil (currently commonly used for chest pain) in people who are 75 years or older with memory complaints.  Download Flyer Here.

EVOKE Studies
We are doing this study to see if the new medicine called semaglutide can help people with early Alzheimer’s disease. This will be done by comparing semaglutide against placebo on the effect on cognition and daily functioning. Alzheimer’s disease is a brain disease that with time can cause dementia. The disease develops slowly and affects memory and other brain functions. As the disease gets worse, the person may need help with basic activities in their daily life.

What will this study look at?
This study will look mainly at changes in cognition (memory and other brain functions) and on daily functioning during treatment with semaglutide or placebo.

This is done by:

  1. Comparing the tests taken at the start of the study with those taken at end of the study
  2. Collecting information about your health, cognition, ability to perform daily activities and general wellbeing
  3. Taking different blood samples and measurements during the study to monitor your health.

Conditions for being considered for participating in the study:

  • You (may) have early Alzheimer’s disease.
  • You are at least 55 years old and not older than 85 years.
  • You have a study partner (a next of kin or someone you have a close relationship to), who is willing to take part in the study and share information about you. Your study partner may also accompany you during discussions with the study doctor.

Download the study flyer

The Alzheimer Prevention Trials Webstudy (APT)
The APT Webstudy - aptwebstudy.org - is an online memory and thinking research tool aimed at accelerating enrollment into Alzheimer’s clinical trials by identifying and tracking individuals who may be at higher risk for developing Alzheimer’s. Participation in the APT Webstudy involves taking online memory and thinking testing four times per year. You may be eligible to participate if you are age 50 or older and are interested in being part of future Alzheimer’s disease prevention trials. Click here to download the study flyer.

The AHEAD Study
The purpose of the AHEAD study is to evaluate whether BAN-2401, a study drug, can help reduce the risk of developing Alzheimer’s disease dementia among individuals who are cognitively normal and have intermediate or elevated levels of amyloid. Participation in this research study will involve visits every two to four weeks over a four-year period to receive the study drug via infusion. Participants will receive either the study drug or a placebo. You may be eligible to participate if you are ages 55-80, are in good general health, and are able to have an MRI scan. 

Click here to download the study flyer
Click here for the AHEAD study FAQ factsheet

The INVOKE study  Recruitment and study enrollment are currently on hold, please check back for updates

The purpose of the INVOKE study is to determine whether a new medication can delay the disease progression in those with early Alzheimer’s disease. Participation in this study lasts about two years and involved monthly infusions of a study drug or placebo. You may be eligible if you are 50-85 years old, have early Alzheimer’s disease and do not live in a long-term care or skilled nursing home.

VIVA-MIND Clinical Trial

The University of Kentucky Sanders-Brown Center on Aging is a site for the VIVA-MIND clinical trial, designed especially for early AD

The VIVA-MIND trial is designed to determine if the study drug, varoglutamstat, can stabilize or slow memory and thinking problems that increase in early AD.

In early AD, a specific and toxic form of the amyloid protein accumulates in the brain. This toxic protein, called N3pE, appears to damage brain cells and surrounding tissues and activates a strong inflammatory response.

The amyloid protein N3pE is not found in healthy individuals and increases with AD progression. VIVA-MIND researchers suspect that N3pE may play a major role in the decline of memory and thinking skills in early AD.

While many older adults feel as though their memory isn’t as good as it used to be, there are distinct differences between normal cognitive aging and the decline observed in people on the AD trajectory. People with early AD experience a measurable decline in memory, verbal ability, decision-making, and judgment.

Click here for the Viva Mind informational flyer
Click here for the Viva Mind tri-fold brochure

AMOR-KY Study

Assessment of Medication Optimization in Rural Kentucky Appalachian Patients With Mild Cognitive Impairment or Dementia
The AMOR-Kentucky study will examine the impact of a pharmacist-physician patient-centered medication therapy management deprescribing intervention to address inappropriate medication use in patients with cognitive impairment in underserved, lower socioeconomic populations in rural Appalachian Kentucky. The results of this study will provide valuable insights on how to expand and implement deprescribing interventions using telemedicine to reduce the prevalence and the associated healthcare costs of medication-related problems in patients with mild cognitive impairment, Alzheimer's disease, and other dementias in rural areas throughout the US. The investigators will assess the potential use of telemedicine in this population by performing an initial single-arm, unblinded study of the medication therapy management (MTM) describing intervention in rural/underserved Kentucky Appalachian populations with cognitive impairment and/or dementia using potentially inappropriate medications (n=50). Following initial recruitment and clinical evaluation, engaged participants will have their medication list reviewed by a pharmacist-clinician team to identify targets for deprescribing intervention. The intervention will be engaged remotely with the participant and their caregiver, and the MTM team at 4 weeks post initial evaluation and then reinforced at a 3-month timepoint. This approach will be carried forward through a telemedicine practice at the University of Kentucky that is comprised of approximately 500 patient-caregiver dyads throughout rural areas of Appalachian Kentucky.

Download the AMOR-KY Flyer

The DIVERSE VCID Study

As awareness of dementia increases, it is common for individuals to seek clinical evaluation for cognitive complaints.
Black American and Hispanic/Latinx Americans are at greater risk than White Americans for developing dementia, likely reflecting historical and present-day systemic racism and social inequities that affect brain health. In fact, social determinants of health strongly contribute to the increased prevalence of vascular brain disease in older adult populations from diverse backgrounds. Neuroimaging studies performed as part of cognitive assessment frequently identify incidental White Matter Hyperintensitites (WMH), usually ascribed to microvascular disease by radiologists, raising patient concerns about their brain health and future risk for dementia.
To date, however, we are not aware of any studies that have comprehensively examined the impact of individual and combined MRI measures of white matter injury on cognitive performance among a diverse, non-demented, stroke free population with cognitive complaints over an extended period of observation. To study this problem directly, the US National Institute of Neurological Disorders and Stroke (NINDS) has commissioned Diverse VCID, a 6-year study of 2,250 Americans from diverse backgrounds to understand the role that WMH play in developing Alzheimer's disease and other dementias. The University of Kentucky Sanders-Brown Center on Aging is a partner site for this study.

The results of this study will be used to develop and validate a predictive risk model to inform future care.

Download DIVERSE VCID Study Flyer

The ADVISE Study

The Sanders-Brown is a participating site for the ADVISE study, a study of the effects of CY6463 in participants with Alzheimer's Disease with vascular pathology. This study is being conducted to test the safety, tolerability, and pharmacokinetics of the investigational drug CY6463 compared with placebo in individuals who are aged 60 years or older and have Alzheimer's disease (AD) along with common cardiovascular risk factors.

Download the ADVISE Informational Flyer

Social and Behavioral Studies


Harmony at H.O.M.E.

Are You a Caring for Someone with Dementia? Researchers at the University of Kentucky invite you to participate in a research study which offers the Harmony at H.O.M.E. (Help Online Modifying the Environment) telehealth program. The program provides training and tools for care partners to assess and modify the home to promote activity engagement and behavior regulation for the person with dementia. This study is led by The University of Kentucky Sanders-Brown Center on Aging faculty member Elizabeth Rhodus, Ph.D.
For more information, please click the following link:  https://www.ccts.uky.edu/participate-research/current-studies/are-you-caring-someone-dementia

Download Flyer

Ongoing Studies Closed for Enrollment

A4: Anti-Amyloid for Asymptomatic Alzheimer’s

The purpose of the A4 study is to evaluate the study treatment (solanezumab) for people with normal cognition who are at risk for developing Alzheimer’s disease on the basis of having biomarker evidence of amyloid. This study will test the hypothesis that decreasing amyloid burden during the preclinical stages of Alzheimer’s disease will delay future cognitive decline. Participants will receive treatment for three years with either the anti-amyloid infusion drug or the placebo. (www.a4study.org). You may be eligible to participate if you are ages 65-85, have normal cognition, and are able to have an MRI scan. 


BAN-2401

The purpose of the BAN-2401 study is to examine whether an anti-amyloid medication may slow or stop the progression of Alzheimer’s disease in people with mild cognitive impairment and mild Alzheimer’s disease. We hope to find out whether the study medication can reduce the amount of amyloid in the brain that might be causing the memory and thinking problems. Participation in this research study lasts two years and involves bi-weekly infusions of the study drug or a placebo (www.nia.nih.gov/alzheimers/clinical-trials/ban2401-early-alzheimers-disease). You may be eligible to participate if you are ages 50 or older and have either mild cognitive impairment or mild Alzheimer’s disease. 

Clarity-AD

The purpose of the Clarity study is to evaluate whether BAN2401, a study drug, may slow or stop the progression of memory problems among individuals with mild cognitive impairment or mild Alzheimer’s disease. Participation in this research study will involve visits every two weeks over an 18-month period to receive the study drug via infusion. Participants will receive either the study drug or a placebo. An extension is currently planned for individuals who complete the study to have the chance to be guaranteed the drug for up to two years. You may be eligible to participate if you are ages 50-90, are in good general health, and are able to have an MRI scan. Click here to download the study flyer.

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