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A Study of Neurodegeneration and Neuronal Fluctuations in Lewy Body Disease and Alzheimer's Disease

Neurodegeneration and Neuronal Fluctuations in Lewy Body Disease and Alzheimer Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06057909
Enrollment
90
Registered
2023-09-28
Start date
2024-04-05
Completion date
2027-06-01
Last updated
2026-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease, Healthy, Lewy Body Disease

Brief summary

The purpose of this research study is to investigate how the brain, memory, thinking, and motor behavior change both in individuals with movement and/or cognitive disorders, as well as healthy individuals. Researchers will look at measurements of memory, thinking, brain wave and muscle activity, daily functioning, and brain scans to learn more about brain disorders such as Alzheimer disease and Lewy body disease.

Interventions

DIAGNOSTIC_TESTMagnetic Resonance Imaging

Test that looks at the structure of the brain.

DIAGNOSTIC_TESTElectroencephalography

Non-invasive technique to measure brain waves

DIAGNOSTIC_TESTElectromyography

Technique to evaluate muscle activity

Sponsors

Mayo Clinic
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 95 Years
Healthy volunteers
Yes

Inclusion criteria

* Use English as their primary language. * Be willing to undergo health and cognitive assessments, as well as brain MRI and EEG study. * Will be encouraged to have an available study partner (also called a "co-participant") who is familiar with the participant's daily functioning. * This study will be limited to healthy individuals, and patients who have a clinical diagnosis made by a board-certified neurologist of Lewy body disease or Alzheimer disease. * All individuals must be capable of providing informed consent and complying with the trial procedures. Realizing the challenge of obtaining informed consent from cognitively impaired individuals, time is specifically scheduled to foster an informative, supportive interview with the participant and caregiver/legal guardian (typically a spouse or child according to Arizona law and IRB guidelines). * Ongoing participation will be maintained by strict adherence to inclusion/

Exclusion criteria

, clinical appropriateness (as determined by participant's physician and proxy/family), as well as by expressed wishes of family members/caregivers/proxy discussed at each study visit (as appropriate). * All participants will receive copies of the signed ICFs (including signatures of those obtaining consent). * All participants have the right to withdraw from the study at any time.

Design outcomes

Primary

MeasureTime frameDescription
Diffusion-weighted MRI (dMRI)BaselineMeasures diffusion of water molecules and cellular-level constraints
Electroencephalography (EEG)BaselineMeasures brain-wave activity

Countries

United States

Contacts

CONTACTSara Dresler
dresler.sara@mayo.edu480-301-6279
PRINCIPAL_INVESTIGATORShannon Chiu, MD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026