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Clinical Trials/NCT06472557
NCT06472557
Recruiting
Not Applicable

Spinocerebellar Ataxia Type 27B Natural History Study (SCA27B-NHS)

University Hospital Tuebingen9 sites in 4 countries300 target enrollmentJune 4, 2024

Overview

Phase
Not Applicable
Intervention
SCA27B risk subjects
Conditions
Spinocerebellar Ataxia Type 27B
Sponsor
University Hospital Tuebingen
Enrollment
300
Locations
9
Primary Endpoint
Friedreich Ataxia Rating Scale - Neurological Examination Part E (upright stability) from baseline to 2-year follow-up
Status
Recruiting
Last Updated
26 days ago

Overview

Brief Summary

This international, multi-center, multi-modal, and prospective observational cohort study aims to validate trial outcomes for capturing disease progression in Spinocerebellar Ataxia Type 27B (SCA27B), with combined multi-modal capture of clinical outcome assessments, digital-motor assessments, and molecular biomarkers.

Detailed Description

The investigators will perform an international, multi-center, multi-modal, and registry-based standardized prospective Natural History Study (NHS) in Spinocerebellar Ataxia Type 27B (SCA27B), including the presymptomatic phase of the disease (i.e. presymptomatic subjects at risk for SCA27B). Participants will be assessed annually. Clinical data, including clinician-reported outcomes and patient-focused outcomes, will be entered into a clinical database customized to the requirements of this specific study (SCA27B Registry; www.ataxia-registries.org). Digital-motor outcomes comprise digital gait assessment by wearable sensors, and digital assessment of upper limb movements by Q-Motor. At all study visits, participants will be asked to donate biosamples; and participants can elect to participate in sampling of blood, urine, CSF, and/or a skin biopsy. Based on this multimodal protocol, the study aims to determine the most sensitive, comprehensive, and reliable outcome measures for future therapeutic trials in SCA27B.

Registry
clinicaltrials.gov
Start Date
June 4, 2024
End Date
December 31, 2028
Last Updated
26 days ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Prof. Dr. Matthis Synofzik

Principal Investigator, Leading Consultant

University Hospital Tuebingen

Eligibility Criteria

Inclusion Criteria

  • SCA27B: genetic diagnosis of ≥250 uninterrupted GAA repeat expansions in FGF14
  • SCA27B risk subject: asymptomatic first-degree relative of SCA27B participant with known or unknown carrier status
  • 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

  • SCA27B: Missing informed consent
  • SCA27B risk subjects: Missing informed consent
  • Unrelated healthy controls: Missing informed consent, or concurrent neurological, orthopedic, or other diseases interfering with the motor assessments

Arms & Interventions

SCA27B risk subjects

First-degree relatives at risk for SCA27B, both with known and unknown carrier status, will be included to capture presymptomatic disease stages. Target sample size for the risk cohort is 50 participants

Unrelated healthy controls

Unrelated healthy controls may undergo the same study procedures as the SCA27B cohort to determine age-related effects on the multimodal outcomes. Target sample size for the control cohort is 50.

SCA27B

Participants with genetically confirmed SCA27B (OMIM 620174), i.e. ≥250 uninterrupted GAA repeat expansions in FGF14, will be recruited. Target sample size for the SCA27B cohort is 200 participants.

Outcomes

Primary Outcomes

Friedreich Ataxia Rating Scale - Neurological Examination Part E (upright stability) from baseline to 2-year follow-up

Time Frame: 24 months

Severity of ataxia in the gait and balance domain will be assessed by application of part E of the neurological examination of Friedreich Ataxia Rating Scale (FARS-E). The total score is calculated as the sum of 7 items, yielding a total score between 0 and 28. Hereby, higher FARS-E scores indicate more severe functional impairment.

Secondary Outcomes

  • Change of Scale for the Assessment and Rating of Ataxia (SARA) from baseline to 2-year follow-up(24 months)
  • Patient Global Impression of Change (PGI-C) from baseline to 1-year and 2-year follow-up(24 months)
  • Friedreich Ataxia Rating Scale - Activities of Daily Living (FARS-ADL) from baseline to 2-year follow-up(24 months)
  • Digital gait and balance assessment from baseline to 2-year follow-up(24 months)

Study Sites (9)

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