CAUTION: Investigational device. Limited by Federal (or United States) law to investigational use.
Alzheimer's Disease Clinical Study
U: The Mind Company is currently enrolling participants for a clinical study of Axis, an investigational non-invasive brain stimulation device. This page provides information to help you determine whether you or someone you know may be eligible to participate.
About This Study
Who Can Participate
You may be eligible if you:
- Are between 55 and 85 years of age
- Have a diagnosis of mild-to-moderate Alzheimer's disease
- Have a designated study partner (caregiver or family member) who can attend sessions with you
- Are able to provide informed consent or have a legally authorised representative who can
You are not eligible if you:
- Have a pacemaker, cochlear implant, or other active implanted device
- Have a history of epilepsy or unprovoked seizures
- Have active psychiatric conditions that would interfere with participation
- Have metal implants in or around the head
- Are currently enrolled in another interventional clinical study
What's Involved
- [NUMBER — CONFIRM] in-clinic stimulation sessions over [DURATION — CONFIRM] weeks
- Each session lasts approximately [SESSION LENGTH — CONFIRM] minutes
- Sessions take place at [LOCATION — CONFIRM]
- You will also complete brief cognitive assessments at the start, midpoint, and end of the study
- Participation is voluntary and you may withdraw at any time
How to Express Interest
If you are interested in learning more or wish to check your eligibility, please contact our research team:
We will respond within [X] business days to discuss next steps. Expressing interest does not commit you to participation.
This study is registered on ClinicalTrials.gov.
Identifier: NCT07182058
Axis is an investigational device and has not been approved by the U.S. Food and Drug Administration. This page is intended for individuals considering participation in a clinical study, not for promotional purposes.