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Multi-Modal Digital Monitoring of Disease Symptoms in Spinocerebellar Ataxia

25 settembre 2026 aggiornato da: BioSensics

This is an observational study. Subjects with a documented diagnosis of spinocerebellar ataxia (SCA) will be screened and recruited to participate at two clinical sites: Johns Hopkins University (JHU) and Columbia University (CU).

Researchers at BioSensics, JHU, and CU will use wearable sensors computerized speech, psychomotor, and ocular assessments to evaluate the feasibility of using digital health technologies to monitor symptoms in SCA. Researchers will also measure the Scale for the Assessment and Rating of Ataxia (SARA) and other SCA clinical assessments.

The solution will be deployed for 25 participants with SCA for approximately 12 months with 5 study visits (Screening/Baseline, Day 1, Day 30, Day 90, Day 180, Day 360).

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Descrizione dettagliata

The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of rare, autosomal dominant neurodegenerative disorders characterized by progressive degeneration of the cerebellum and its connecting pathways. The four most common subtypes (SCA1, SCA2, SCA3, and SCA6) are caused by expanded polyglutamine-coding CAG repeats, and collectively account for the majority of dominantly inherited ataxias worldwide. The cardinal feature across subtypes is progressive ataxia affecting gait, stance, limb coordination, and speech, frequently accompanied by oculomotor abnormalities and, in some subtypes, extracerebellar signs such as spasticity, peripheral neuropathy, and parkinsonism. Symptoms typically begin in adulthood and progress over many years, leading to severe disability and reduced life expectancy.

The principal means of measuring ataxia severity is the Scale for the Assessment and Rating of Ataxia (SARA), which is the most widely applied clinical outcome assessment (COA) for genetic ataxias and has been used as the primary endpoint in large natural history cohorts and randomized controlled trials. Although the SARA has demonstrated good inter-rater reliability and has been validated across multiple SCA subtypes, it is inherently subjective and semi-quantitative, requires trained personnel to administer, and may not be sufficiently sensitive to detect incremental but clinically meaningful changes over short follow-up intervals.

Movement-associated symptoms are a core feature of SCA and have a substantial negative impact on quality of life. Impairments in gait and balance contribute to falls and loss of independence, while dysarthria and impaired limb coordination affect communication and activities of daily living. Because these assessments are conducted infrequently, typically in a clinic setting, they may not accurately represent an individual's true functional status during everyday life. However, the increasing understanding of disease pathomechanisms and the development of gene-targeting and other novel therapeutic approaches have raised expectations for disease-modifying treatments. The key challenge in developing new therapeutics for SCA and other neurological disorders is that current disease assessment is largely subjective and requires in-person, in-clinic evaluation.

Digital measures, such as those proposed in this study, can provide objective, sensitive, and real-world assessments of how individuals are functioning. A growing body of evidence demonstrates that digital biomarkers derived from body-worn inertial sensors can quantify ataxia-specific gait and balance impairments, and correlate strongly with clinician-rated SARA scores.

Beyond gait and balance, multi-modal digital assessment of speech, hand function, and oculomotor control may capture complementary domains of cerebellar dysfunction that are affected in SCA. Acoustic analysis of speech can quantify dysarthria, finger tapping can characterize upper-limb bradykinesia and dysrhythmia, and oculomotor testing can capture saccadic and antisaccadic abnormalities that are characteristic of cerebellar disease.

Thus, a system that can objectively, sensitively, and frequently monitor multiple clinical domains (motor, speech, and oculomotor function) is necessary to understand the pattern of evolving impairment in individuals with SCA and to support the identification of endpoint measures for therapeutic trials. This study will evaluate the feasibility of a multi-modal digital monitoring platform in a cohort of individuals with SCA and will characterize the relationship between digital measures and established clinical and patient reported outcomes.

Tipo di studio

Osservativo

Iscrizione (Stimato)

25

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Maryland
      • Lutherville, Maryland, Stati Uniti, 21093
        • Johns Hopkins University School of Medicine
        • Contatto:
        • Investigatore principale:
          • Liana Rosenthal, MD PhD
    • New York
      • New York, New York, Stati Uniti, 10032
        • Columbia University Irving Medical Center/Neurological Institute of New York
        • Investigatore principale:
          • Sheng-Han Kuo, MD
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Adults with SCA

Descrizione

Inclusion Criteria:

  • Male or female, aged 18-75 years
  • Fluent in English (able to speak and read)
  • Able to ambulate at least 10 meters independently or with a cane, without other assistive devices, as determined by the investigator
  • Able to independently perform all study activities safely, as determined by the investigator
  • Willing and able to provide informed consent and comply with all study procedures
  • Genetically or clinically confirmed diagnosis of spinocerebellar ataxia (SCA 1, 2, 3, or 6)

Exclusion Criteria:

  • Individuals who are unable to ambulate at least 10 meters independently or with a cane.
  • Individuals with a neurological, medical, or psychiatric condition (other than SCA) that, in the investigator's judgment, would interfere with safe participation in study activities or confound the assessment of ataxia
  • Pregnant individuals, due to potential changes in gait and physical activity during pregnancy
  • Any condition that, in the investigator's judgment, would prevent the participant from completing the study procedures safely

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: COHORT
  • Prospettive temporali: PROSPECTIVE

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Physical Activity Monitoring - Daily Number of Steps (count)
Lasso di tempo: 12 months

Following each clinical visit, participants will be asked to wear a PAMSys pendant sensor, PAMSys ULM wrist sensors, and PAMSys Gait for 7 days at home. The average daily number of steps will be measured using the PAMSys pendant.

12 months
Physical Activity Monitoring - Total number of goal-directed movement (GDM)
Lasso di tempo: 12 months

Following each clinical visit, participants will be asked to wear a PAMSys ULM sensor, a wearable sensor for long-term monitoring of upper limb and activities of daily living (ADL). The sensor will record the daily number GDMs as participants perform ADLs.

12 months
Physical Activity Monitoring - Stride Velocity (m/s)
Lasso di tempo: 12 months

Following each clinical visit, participants will be asked to wear a PAMSys Gait sensor, a wearable sensor for long-term monitoring of gait during activities of daily living (ADL). The sensor will record the average stride velocity (m/s) during ADLs.

12 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Scale for the Assessment and Rating of Ataxia (SARA)
Lasso di tempo: 12 months

The SARA is an 8-item clinical sale to measure severity and progression of cerebellar ataxia. Total scores range from 0 (no ataxia) to 40 (most severe ataxia).

12 months
Digital Speech Assessment - Intelligibility (%)
Lasso di tempo: 12 months

Using a study tablet, participants will read the Rainbow Passage. Intelligibility is a digital measure of speech clarity that determines how easily a listener can understand spoken words. Intelligibility ranges scores from 0 to 100%

12 months
1 Minute Walk Test - Gait Speed (m/s)
Lasso di tempo: 12 months

Performed at each clinical visit, the participant will complete the 1 Minute Walk Test. Gait speed will be measured using LEGSys.

12 months
Digital Occulomotor Assessments - Median velocity (pixel/s)
Lasso di tempo: 12 months

Using a study tablet, participants will perform a series of oculomotor assessments (saccades). The video will be analyzed to calculate the median velocity of the pupil during saccade movements.

12 months
EuroQoL 5-Dimension 5-Level questionnaire (EQ-5D-5L)
Lasso di tempo: 12 months

The EQ-5D-5L is a standardized 5-item tool used to measure health-related quality of life. EQ-5D-5L scores are interpreted by analyzing three distinct components: a 5-digit health profiles. Each dimension uses five severity levels (1 = no problems, 2 = slight, 3 = moderate, 4 = severe, 5 = extreme/unable to).

12 months
1 Minute Walk Test with Cognitive Load- Gait Speed (m/s)
Lasso di tempo: 12 months

Performed at each clinical visit, the participant will complete the 1 Minute Walk Test with cognitive load (counting backwards). Gait speed will be measured using LEGSys.

12 months
Timed Up and Go (TUG) - Sit to Stand duration (s)
Lasso di tempo: 12 months

Performed at each clinical visit, the participant will complete the TUG Test. Sit to stand duration will be measured using LEGSys.

12 months
30S Chair Sit to Stand - Sit to Stand duration (s)
Lasso di tempo: 12 months

Performed at each clinical visit, the participant will complete the 30S Chair Sit to Stand Test. Sit to stand duration will be measured using LEGSys.

12 months
Digital Occulomotor Assessment - Median duration (s)
Lasso di tempo: 12 months

Using a study tablet, participants will perform a series of oculomotor assessments (saccades). The video will be analyzed to calculate the median duration of the pupil during saccade movements.

12 months
EQ-VAS (Visual Analog Scale)
Lasso di tempo: 12 months

The EQ VAS: The participant self-rates their overall health on a vertical thermometer-like scale from 0 to 100, where 100 is the best health the participant can imagine, and 0 is the worst health the participant can imagine.

12 months

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Digital Fine Motor Control Assessment - Number of taps (count)
Lasso di tempo: 12 months

Using a study tablet, participants will perform a series of tapping tests. The tablet will calculate the count of all recorded taps made by a finger on the screen.

12 months
Digital Fine Motor Control Assessment - Average tap rate (s)
Lasso di tempo: 12 months

Using a study tablet, participants will perform a series of tapping tests. The tablet will calculate the number of taps per second.

12 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 dicembre 2026

Completamento primario (Stimato)

31 dicembre 2028

Completamento dello studio (Stimato)

31 gennaio 2029

Date di iscrizione allo studio

Primo inviato

16 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

25 settembre 2026

Primo Inserito (Effettivo)

1 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

25 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • BioDigit SCA-02

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .