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Recruiting No phase listed Observational Accepts healthy volunteers

PREVENT ALL ALS Study

ClinicalTrials.gov ID: NCT06581861

Public ClinicalTrials.gov record NCT06581861. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 7, 2026, 8:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

PREVENT ALL ALS - Longitudinal Biomarker Study for Participants Who Are Genetically at Risk for Amyotrophic Lateral Sclerosis (ALS)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The ALL ALS Clinical Research Consortium is establishing research to collect a wide range of samples, clinical information and measurements from Amyotrophic Lateral Sclerosis (ALS) symptomatic, ALS gene carriers and control cohorts. This consortium is begin funded by the National Institutes of Health/National Institute of Neurological Disorders and Stroke (NIH/NINDS) and managed by two clinical coordinating centers (CCC) at Barrow Neurological Institute and Massachusetts General Hospital. The clinical sites are distributed across the country, and led by a group of collaborative principal investigators. Once data and samples are collected and harmonized, it will be made available to research community for future research into ALS and related neurological diseases. PREVENT protocol is specific for asymptomatic participants who are genetically at risk for ALS. The participants will be followed for up to 36 months (3 years), and will include 4 in-person on-site visits once a year and 6 off-site(remote) visits once in 4 months. The study includes collection of medical history, clinical outcomes, and blood samples once in 4 months. Additionally, the participants will complete patient reported outcomes and speech recordings once in 4 months. Participants may also provide optional Cerebrospinal Fluid (CSF) samples.The participants may also opt into a sub-study if they are interested in genetic testing for ALS causative genes. The sub-study will involve a minimum of 3 visits over a course of 2-3 months. This will include a screening/pre-test genetic counseling visit, a return of genetic results and a post-test counseling visit.

Study identification

NCT ID
NCT06581861
Recruitment status
Recruiting
Study type
Observational
Phase
Not listed
Enrollment
600 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 25, 2024 (Actual)
Primary completion
Jan 31, 2029 (Estimated)
Completion
Jul 25, 2029 (Estimated)
Last update posted
Aug 24, 2026

2024 – 2029

United States locations

U.S. sites
31
U.S. states
26
U.S. cities
31
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35294 Recruiting
Barrow Neurological Institute Phoenix Arizona 85013 Recruiting
University of California San Diego La Jolla California 92037 Recruiting
University of California Irvine Orange California 92868 Recruiting
University of California, San Francisco San Francisco California 94143 Recruiting
University of Colorado Anschutz Medical Campus Aurora Colorado 80045 Recruiting
Hospital for Special Care New Britain Connecticut 06053 Recruiting
Georgetown University Washington D.C. District of Columbia 200007 Recruiting
Mayo Clinic Jacksonville Florida 32224 Recruiting
Saint Alphonsus Regional Medical Center Boise Idaho 83704 Recruiting
Northwestern University Chicago Illinois 60611 Recruiting
Indiana University Indianapolis Indiana 46202 Recruiting
John Hopkins University Baltimore Maryland 21205 Recruiting
Nih/Ninds Bethesda Maryland 20892 Recruiting
Massachusetts General Brigham Boston Massachusetts 02145 Recruiting
University of Michigan Ann Arbor Michigan 48109 Recruiting
Henry Ford Health Detroit Michigan 48202 Recruiting
University of Minnesota Minneapolis Minnesota 55455 Recruiting
Washington University St Louis Missouri 63110 Recruiting
University of Nebraska Medical Center Omaha Nebraska 68198 Recruiting
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 Recruiting
Columbia University New York New York 10032 Recruiting
Duke University Durham North Carolina 27705 Recruiting
Ohio State University Columbus Ohio 43221 Recruiting
Providence ALS Center Portland Oregon 97213 Recruiting
Penn State Health Hershey Pennsylvania 17033 Recruiting
Temple University Philadelphia Pennsylvania 19140 Recruiting
Texas Neurology Dallas Texas 75206 Recruiting
University of Utah Salt Lake City Utah 84132 Recruiting
Virginia Commonwealth University Richmond Virginia 23298 Recruiting
University of Washington Seattle Washington 98195 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06581861, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 24, 2026 · Synced Oct 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06581861 live on ClinicalTrials.gov.

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