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NCT06581861Active, not recruiting

PREVENT ALL ALS Study

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

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
600 (estimated)
First submitted
21 Aug 2024
Start date
25 Jul 2024
Primary completion date
31 Jan 2029
Lead sponsor
St. Joseph's Hospital and Medical Center, Phoenix
NCT number
NCT06581861

What you commit to

  • Study type: Observational
  • Planned participants: 600
  • From 25 Jul 2024 to the primary completion date, 31 Jan 2029
  • 32 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of anticoagulant medication or antiplatelet medications (aside from aspirin 81 mg) that cannot be safely withheld prior to lumbar puncture.

Other illness

  • Significant cognitive impairment, clinical dementia, or unstable psychiatric illness, including psychosis, active suicidal ideation, suicide attempt, or untreated major depression \<= 90 days (about 3 months) of screening, which in the opinion of the Investigator would interfere with the study procedures
  • Clinically significant, unstable medical condition (e.g., cardiovascular instability, systemic infection, untreated thyroid dysfunction, malignant and potentially progressive cancer) that would render the participant unlikely to be able to complete 12 months of follow-up, according to Investigator's judgment
  • Medically unable to undergo lumbar puncture (LP) as determined by the site investigator (i.e., bleeding disorder, a skin infection at or near the LP site, known or suspected intracranial or intraspinal tumor or other cause of increased intracranial pressure).
  • Allergy to Lidocaine or other local anesthetic agents.
  • Blood dyscrasia, abnormal bleeding diathesis, or the use of dialysis for renal failure.

Other

  • Evidence of neurological signs or symptoms concerning for ALS of FTD, at the discretion of the site investigator which will be communicated to the applicant along with referral for appropriate clinical follow-up.
  • Current pregnancy based on participant self-report
  • Clinical judgement of the site investigator that the participant would be unable to undergo multiple lumbar punctures.

Who the study is looking for

  • Age 18 years or older
  • Capable of providing informed consent
  • Willing to follow study procedures
  • First-degree relative of a known carrier of any ALS causative gene1 (regardless of whether ALS or FTD has actually been symptomatic in the family) OR First-degree relative of an individual with ALS and/or FTD in a family with a "compelling family history" of ALS/FTD, regardless of whether genetic testing has occurred in symptomatic family members. A "compelling family history" is defined as a pedigree with at least 2 close relatives who had ALS or FTD, with at least one of those family members having had ALS.
  • Access to a smartphone, computer, or tablet, and internet (need not be in the home - access to a public library or other available computer with internet connection is sufficient)
  • Age 18 years of age or older
  • Capable of providing informed consent
  • Willing to follow study procedures
  • Currently enrolled in the PREVENT ALS Study

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (32)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHALS-CCT, University of Puerto Rico, Medical Sciences Campus
Coordinator of this site? Confirm its status
San JuanPuerto RicoUnknown status
University of Michigan
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Ann ArborUnited StatesUnknown status
University of Colorado Anschutz Medical Campus
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AuroraUnited StatesUnknown status
John Hopkins University
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BaltimoreUnited StatesUnknown status
Nih/Ninds
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BethesdaUnited StatesUnknown status
University of Alabama Birmingham
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BirminghamUnited StatesUnknown status
Saint Alphonsus Regional Medical Center
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BoiseUnited StatesUnknown status
Massachusetts General Brigham
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BostonUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
Ohio State University
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ColumbusUnited StatesUnknown status
Texas Neurology
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DallasUnited StatesUnknown status
Henry Ford Health
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DetroitUnited StatesUnknown status
Duke University
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DurhamUnited StatesUnknown status
Penn State Health
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HersheyUnited StatesUnknown status
Indiana University
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IndianapolisUnited StatesUnknown status
Mayo Clinic
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JacksonvilleUnited StatesUnknown status
University of California San Diego
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La JollaUnited StatesUnknown status
Dartmouth Hitchcock Medical Center
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LebanonUnited StatesUnknown status
University of Minnesota
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MinneapolisUnited StatesUnknown status
Hospital for Special Care
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New BritainUnited StatesUnknown status
Columbia University
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New YorkUnited StatesUnknown status
University of Nebraska Medical Center
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OmahaUnited StatesUnknown status
University of California Irvine
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OrangeUnited StatesUnknown status
Temple University
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PhiladelphiaUnited StatesUnknown status
Barrow Neurological Institute
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PhoenixUnited StatesUnknown status
Providence ALS Center
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PortlandUnited StatesUnknown status
Virginia Commonwealth University
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RichmondUnited StatesUnknown status
University of Utah
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Salt Lake CityUnited StatesUnknown status
University of California San Francisco
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San FranciscoUnited StatesUnknown status
University of Washington
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SeattleUnited StatesUnknown status
Washington University
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St LouisUnited StatesUnknown status
Georgetown University
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Washington D.C.United StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.