Longevity & AgingResearch PaperOpen Access

Wearable Sensors Are Quietly Revolutionizing Multiple Sclerosis Monitoring

Biosensors capture subtle MS disability signals that traditional clinic visits miss—opening the door to continuous, personalized disease tracking.

Friday, May 15, 2026 0 views
Published in Curr Neurol Neurosci Rep
A person with MS wearing a sleek wrist sensor walks outdoors on a sunlit path, with translucent data graphs floating alongside.

Summary

This 2025 review from Johns Hopkins examines how biosensors and digital wearables are reshaping monitoring of people with multiple sclerosis (MS). Traditional tools like the Expanded Disability Status Scale (EDSS) are coarse, infrequent, and insensitive to subtle change. Accelerometers, inertial measurement units, instrumented walkway mats, pressure-sensing insoles, and specialized bladder and fine-motor sensors now capture gait, balance, physical activity, circadian rhythms, dexterity, and bladder function with far greater precision. A consistent finding across studies is that these technologies detect early, subclinical impairments missed by standard assessments. Longitudinal data suggest wearable-derived metrics may predict brain atrophy and disability progression, pointing toward their eventual role in clinical trials and personalized MS care.

Detailed Summary

Multiple sclerosis is a progressive immune-mediated disease where disability accumulates over years or decades, yet the primary clinical measurement tool—the EDSS—is semi-quantitative, nonlinear, and typically administered only every three to six months. This creates major blind spots for detecting early change, guiding therapy, or powering clinical trials. The authors from Johns Hopkins argue that digital biosensors can fill these gaps by providing continuous, objective, quantitative data across multiple functional domains.

The review covers six core monitoring domains. For physical activity and circadian rhythmicity, accelerometers reliably show that people with MS are more sedentary, more active-to-sedentary transition-prone, and have weaker circadian rhythm amplitude than healthy controls—differences that are amplified in progressive MS. Critically, the HEAL-MS longitudinal cohort found that within-person increases in nighttime activity and decreases in morning activity predicted faster rates of whole-brain and gray matter atrophy over roughly one year, suggesting wearable metrics may serve as leading indicators of neurodegeneration.

For gait, both non-wearable systems (optical motion capture, force platforms, instrumented walkway mats like GAITRite) and wearable IMUs reveal reduced speed, altered stride length, increased stride-to-stride variability, and instability even in early MS patients without clinically apparent disability. Wearables extend this monitoring into real-world community settings, where gait performance is consistently worse than in-clinic measurements—a finding with direct implications for how we interpret trial endpoints. Sensorized cane/crutch tips have even been proposed for patients requiring assistive devices.

Balance assessment using IMU-instrumented versions of classic tests (e.g., Balance Error Scoring System, Romberg) and force platforms demonstrates postural instability in MS that correlates with fall risk and disability. Fine motor function—captured by finger-tapping apps, instrumented stylus devices, dynamometers, and novel textile gloves—detects subtle hand dexterity deficits often missed by standard assessments, including in early disease. Bladder sensors, including wearable ultrasound and electronic bladder diaries, offer objective, non-invasive monitoring of voiding patterns and urgency that surpass subjective questionnaire data.

The overarching theme is that biosensors consistently reveal subclinical impairment that standard clinical measures miss. Longitudinal associations between wearable-derived metrics and brain imaging outcomes suggest predictive validity. However, the field faces challenges: methodological heterogeneity across studies limits cross-study comparison, commercial sleep and autonomic algorithms are not validated in MS populations, and regulatory pathways for integrating these tools into trials remain underdeveloped. Larger longitudinal validation studies are needed before clinical adoption can be recommended broadly.

Key Findings

  • Wearable accelerometers detect more sedentary behavior and weaker circadian rhythms in MS vs. healthy controls, worsening with disability.
  • Nighttime activity increases and morning activity decreases predicted faster brain atrophy in the HEAL-MS longitudinal cohort.
  • Real-world community gait measured by wearables is consistently slower than in-clinic gait, exposing a key gap in trial endpoints.
  • Biosensors capture subclinical gait, balance, and fine motor deficits even in early MS patients with no clinically apparent disability.
  • Bladder wearables and finger-tapping apps provide objective domain-specific data that outperform standard questionnaires and clinical ratings.

Methodology

This is a narrative review of current and emerging biosensor literature in MS, organized by functional domain (physical activity, circadian rhythmicity, gait, balance, fine motor function, bladder). It incorporates cross-sectional and longitudinal studies, including the authors' own HEAL-MS cohort, and synthesizes findings across wearable and non-wearable sensor modalities.

Study Limitations

Significant methodological heterogeneity across studies—different devices, placement sites, analytic pipelines, and outcome definitions—limits cross-study comparisons and generalizability. Commercial wearable sleep and autonomic algorithms have not been validated in MS populations and are likely less accurate in patients with reduced mobility or autonomic dysfunction. Most studies are relatively small and short-term; large-scale longitudinal validation and regulatory-grade standardization are still lacking.

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