Ireland
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Latest
Recruiting Observational

RFC1 Natural History Study

NCT05177809 · tracked via the Priya Life Science Italy tracker
Sponsor
Prof. Dr. Matthis Synofzik
Phase
Observational
Started
2021-12-14
Last updated
2026-03-31

Condition(s) studied

Ataxia

Investigational drug(s) / intervention(s)

Clinical rating scale to measure ataxia disease severity and progression

Clinical rating scale to measure ataxia disease severity and progression: SARA is a clinical scale developed by Schmitz-Hübsch et al which assesses a range of different impairments in cerebellar ataxia. The scale is made up of 8 items related to gait, stance, sitting, speech, finger-chase test, nose-finger test, fast alternating movements and heel-shin test.

Study summary

This international, multi-center, multi-modal and prospective observational study aims to determine the phenotypic spectrum and the natural progression of the RFC1 repeat expansion disease, and to seek and validate digital, imaging, and molecular biomarkers that aid in diagnosis and serve as outcome measures in future clinical trials of this novel, but frequent ataxia with late adult-onset.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * RFC1: genetic diagnosis of bi-allelic pathogenic repeat expansions in RFC1 * Unrelated healthy controls: no signs or history of neurological or psychiatric disease AND * Written informed consent AND * Participants are willing and able to comply with study procedures Exclusion Criteria: * RFC1: Missing informed consent * Controls: evidence of neuropathy, neurodegenerative disease, or movement disorder; inability to give informed consent

Primary outcome measure(s)

  • Change of Scale for the Assessment and Rating of Ataxia (SARA) from baseline to 2-year follow-up. — 24 months
    Severity of ataxia in the RFC1 cohort will be assessed by application of the Scale for the Assessment and Rating of Ataxia (SARA). The total score is calculated as the sum of 8 items, yielding a total score between 0 and 40. Hereby, higher SARA scores indicate more severe disease.

Trial sites (10)

FacilityCityRegionStatus
Department of Neuroscience, Central Clinical School, Monash University Melbourne Victoria Recruiting
Department of Neurology, Ataxia Unit, Universidade Federal de São Paulo São Paulo State of São Paulo Recruiting
Service de Neurologie, Hôpitaux Universitaires de Strasbourg Strasbourg Strasbourg Recruiting
Center for Neurology & Hertie-Institute for Clinical Brain Research, Dept. for Neurodegenerative Diseases Tübingen Baden-Wurttemberg Recruiting
German Center for Neurodegenerative Diseases (DZNE) Bonn North Rhine-Westphalia Recruiting
Department of Neurology University Hospital Schleswig Holstein Lübeck Schleswig-Holstein Recruiting
Università degli Studi di Napoli 'Federico II', c/o AOU Federico II Naples Napoli Recruiting
IRCCS Fondazione Stella Maris Pisa Italy Recruiting
Centre of Brain Research Neurogenetics Research Clinic, University of Auckland Auckland New Zealand Recruiting
Koç University Hospital, KUTTAM-NDAL Istanbul Turkey (Türkiye) Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05177809 on ClinicalTrials.gov ↗ ← All trials in Italy