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Multi-Modal Digital Monitoring of Disease Symptoms in Spinocerebellar Ataxia

2026년 9월 25일 업데이트: 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).

연구 개요

상태

아직 모집하지 않음

상세 설명

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.

연구 유형

관찰

등록 (추정된)

25

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Maryland
      • Lutherville, Maryland, 미국, 21093
        • Johns Hopkins University School of Medicine
        • 연락하다:
        • 수석 연구원:
          • Liana Rosenthal, MD PhD
    • New York
      • New York, New York, 미국, 10032
        • Columbia University Irving Medical Center/Neurological Institute of New York
        • 수석 연구원:
          • Sheng-Han Kuo, MD
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

Adults with SCA

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 관찰 모델: COHORT
  • 시간 관점: PROSPECTIVE

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Physical Activity Monitoring - Daily Number of Steps (count)
기간: 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)
기간: 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)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Scale for the Assessment and Rating of Ataxia (SARA)
기간: 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 (%)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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

기타 결과 측정

결과 측정
측정값 설명
기간
Digital Fine Motor Control Assessment - Number of taps (count)
기간: 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)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 12월 15일

기본 완료 (추정된)

2028년 12월 31일

연구 완료 (추정된)

2029년 1월 31일

연구 등록 날짜

최초 제출

2026년 9월 16일

QC 기준을 충족하는 최초 제출

2026년 9월 25일

처음 게시됨 (실제)

2026년 10월 1일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 1일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 25일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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