NIH-funded research P30 center grant

UCSF Clinical Core for Dementia and Memory Disorders

Official title: Core B - Clinical Core

Funded at University of California, San Francisco · NIH-11378121 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check NIH RePORTER for its current status.

This program collects detailed medical and cognitive information and follows people with early‑onset or atypical Alzheimer's and related dementias to help improve diagnosis and care for diverse communities.

Quick facts

Grant typeP30 center grant
Study typeNIH-funded research
Funding institutionUniversity of California, San Francisco
NIH-funded
Lab location1 site (San Francisco, United States)
Project IDNIH-11378121 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are people with early‑onset, atypical, or frontotemporal forms of dementia (including suspected Alzheimer’s, prion disease, or traumatic encephalopathy) and their caregivers who can return for follow‑up visits.

Less likely to help

People without cognitive concerns or those who cannot travel to UCSF for clinical visits are unlikely to receive direct benefits from participation.

What this research studies

You would receive detailed cognitive testing, medical evaluations, imaging, and biosample collection and be followed over time so clinicians can track how symptoms change. The Core focuses on early‑onset and atypical Alzheimer's, frontotemporal dementia, prion disease, and traumatic encephalopathy and includes substantial Chinese and Latino participation to reflect San Francisco demographics. Collected data and samples are shared with researchers at UCSF and beyond to define molecular subtypes and predictors of disease trajectory. The Core also works to validate practical cognitive assessments and care models that can be used in everyday clinical practice.

Why it matters

Potential benefit: If successful, this could lead to earlier, more accurate diagnoses and care tailored to specific dementia subtypes and to better tools for diverse patient groups.

How similar studies have gone: Other Alzheimer Disease Research Centers have successfully used deep phenotyping and longitudinal follow‑up to improve understanding of disease subtypes and diagnostic tools, so this approach is well established.

Where this research is happening

  • University of California, San Francisco
    San Francisco, United States
    Active

Researchers

  • Principal investigator: Possin, Katherine Laurel — University of California, San Francisco
  • Study coordinator: Possin, Katherine Laurel

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About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.