Portland, ORNCT06613204Now EnrollingIRB Ready

Frontotemporal Dementia Clinical Trial in Portland, OR

Access cutting-edge frontotemporal dementia treatment through this clinical trial at a research site in Portland. Study-provided care at no cost to qualified participants.

Sponsored by Oregon Health and Science University

Quick Self-Assessment

See if you qualify for this Portland location

Preparing your pre-screening questions…

Expert Care in Portland

Access frontotemporal dementia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related frontotemporal dementia treatment provided free

Apply for This Portland Location

Check if you qualify for this frontotemporal dementia clinical trial in Portland, OR

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Portland

    Convenient for OR residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Portland site if eligible
  4. 4Begin participation

About This Frontotemporal Dementia Study in Portland

The purpose of this nationwide study is to test STELLA-FTD (Support via Telehealth: Living and Learning with Advancing Alzheimer's Disease)-FTD, an intervention to specifically address the needs of family Care Partners of persons with frontotemporal degeneration (FTD). STELLA-FTD is a multicomponent videoconference-based intervention designed to facilitate effective use of community and peer resources to foster effective management of behavioral and psychological symptoms of dementia. The study is recruiting families from across the United States.

Sponsor: Oregon Health and Science University

Who Can Participate

Inclusion Criteria

Family Care Partner
Adult caring for family member with FTD.
Provides 4 or more hours of care/week. Does not have to reside with.
Identifies at least 2 moderately upsetting behaviors in the person with FTD.
Speaks and understands English to be able to participate in intervention.
Owns a telephone (smartphone, cell phone or landline).
Has email and mailing address to receive computer, study materials and surveys.
Provides informed consent to participate in the research.
Lives in the US Inclusion Criteria: Person with FTD
Diagnosis of FTD
Family member of a Care Partner (this can be a relative, spouse, or close kin that is considered family).
Lives in US

Exclusion Criteria

Person with FTD
No Frontotemporal Degeneration diagnosis.
Unable to leave Care Partner during STELLA-FTD sessions.
Enrolled in hospice. Exclusion Criteria: Family Care Partner
Unable to find activity for Care Recipient during STELLA-FTD sessions to allow Care Partner to work privately with Guide and other Care Partners.
Hearing and/or vision problems severe enough to prevent participation.
Refuses to be video-recorded during STELLA-FTD sessions.
Unwilling or unable to adequately follow study instructions and participate in study procedures.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Portland?

Yes, this clinical trial (NCT06613204) has an active research site in Portland, OR that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Frontotemporal Dementia Treatment Options in Portland, OR

If you're searching for frontotemporal dementia treatment options in Portland, OR, this clinical trial (NCT06613204) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Portland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced frontotemporal dementia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all frontotemporal dementia clinical trials near you to find additional studies recruiting in your area.

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Ready to Join in Portland?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Portland, OR