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Набор скоро начнётся NCT07220707

Wearable Technology to Assist Gait and Mobility in the Older Adult

Наблюдательное Older Adults Who Use an Assistive Device for Mobility

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Wearing the Accelera device.
Кому может быть актуально
Состояния в реестре: Older Adults Who Use an Assistive Device for Mobility. Базовые параметры: от 65 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Pilot Study to Assess the Role of Accelera Stochastic Resonance Wearable Technology to Assist Gait and Mobility in the Older Adult

Обзор

This study assesses whether a small wearable ankle bracelet device can improve gait and mobility in the older adult. Before wearing the bracelet, participants will answer a brief questionnaire, have gait and mobility assessed via 3 CDC approved tests and an app, then wear the device and repeat these gait and mobility assessments, and complete a questionnaire.

Подробное описание

This is a pilot, observational study with 20 volunteers at Jefferson's Ferry Independent Living. Before the Accelera ankle bracelets are applied, participants will complete a pre-study questionnaire. They will then complete 3 tests that the Centers for Disease Control (CDC) recommends for fall risk assessment, namely the chair stand test, 4-point balance test, and timed up and go test, while using their usual mobility assist devices. If the participants provide optional consent, they will undergo video-based gait/mobility analysis of information derived from the HIPAA compliant Onform video recording app, while they are using their usual mobility assistance devices, if any. In other words, a video recording is made with the app and stored on the apps' HIPAA compliant platform. With the faces obscured, measurements of their gait/mobility will be performed using additional programs as indicated in the Data section. After bracelet application, volunteers will then be encouraged to resume their normal ambulation' (while using their usual mobility assistive devices) for about 30 minutes at the study location as described below. The same 3 tests will be repeated after 30 minutes, along with a post-study questionnaire, and if they consented to video recording above, then repeat videorecording with the Onform video recording app would be performed. With the faces obscured, measurements of their gait/mobility will be performed using additional programs as indicated in the Data section. At this point, the ankle bracelets will be removed - with the subjects having worn them for about 1 hour total. There will be an additional up to 1 hour for completion of the pre- and post-study questionnaires, for a total study session duration of about 1.5 - 2 hours. At each session, we will apply these bracelets to a minimum of 1 patient per session. These sessions will occur at the Wellness Center/gym or other designated area at Jefferson's Ferry 1x per week, with a minimum of one patient for up to 8 patients/week if no holidays, until 20 patients have completed the study. To address infection control, a disposable sock will provide a physical barrier between the device and patient, while still allowing the patient to feel the stochastic resonance.

Вмешательства

  • Устройство Wearing the Accelera device
    Wearing the Accelera device prior to retesting gait and mobility

Первичные конечные точки

  • Performance on mobility/gait assessments and subjective evaluation by participant [Срок оценки: from enrollment to the end of the single study session for that participant]
Вторичные конечные точки (1)
  • sensory thresholds for the device [Срок оценки: while wearing the ankle bracelet device]

Критерии участия

Критерии включения

  • 65+ years old residing at Independent Living at Jefferson's Ferry
  • Express interest in the ankle wearable device
  • Have capacity as measured by being alert and oriented to person, place, and time
  • Can communicate in English and provide written consent
  • Able to walk and stand unsupported by others and feel ankle vibrations at maximum amplitude.
  • Answers "Yes" to at least one: worry about falling, had a fall within last year, feel unsteady when walking, enrolled in a fall prevention program, or use/have used assistive devices, such as canes or walkers

Критерии исключения

Participants are excluded from the study if any of the following criteria apply:

  • Diagnosed with neurodegenerative diseases (such as Parkinson's, Alzheimer's, or Amyotrophic Lateral Sclerosis (ALS))
  • Disability from a stroke or other major neurologic disorder resulting in leg paralysis
  • Active ulcers/rashes/infections on feet or legs, or using orthotics other than arch supports or over the counter knee/ankle supports
  • Significant lymphedema/peripheral edema/or large ankle size that prevents ankle wearable device application or functionality
  • Cannot give written consent
  • Unable to walk today or generally use wheelchairs
  • Unable to participate due to medical or cognitive reasons
  • Any lower extremity amputation other than one toe
  • On anticoagulants or antiplatelet agents other than aspirin
  • Unable to participate due to other medical or cognitive reasons
  • Age under 65 years

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

США · 1 центр
  • Jefferson's Ferry — South Setauket

Публикации

  • Priplata AA, Patritti BL, Niemi JB, Hughes R, Gravelle DC, Lipsitz LA, Veves A, Stein J, Bonato P, Collins JJ. Noise-enhanced balance control in patients with diabetes and patients with stroke. Ann Neurol. 2006 Jan;59(1):4-12. doi: 10.1002/ana.20670. PMID 16287079
  • Priplata AA, Niemi JB, Harry JD, Lipsitz LA, Collins JJ. Vibrating insoles and balance control in elderly people. Lancet. 2003 Oct 4;362(9390):1123-4. doi: 10.1016/S0140-6736(03)14470-4. PMID 14550702
  • Liu W, Lipsitz LA, Montero-Odasso M, Bean J, Kerrigan DC, Collins JJ. Noise-enhanced vibrotactile sensitivity in older adults, patients with stroke, and patients with diabetic neuropathy. Arch Phys Med Rehabil. 2002 Feb;83(2):171-6. doi: 10.1053/apmr.2002.28025. PMID 11833019
  • Galica AM, Kang HG, Priplata AA, D'Andrea SE, Starobinets OV, Sorond FA, Cupples LA, Lipsitz LA. Subsensory vibrations to the feet reduce gait variability in elderly fallers. Gait Posture. 2009 Oct;30(3):383-7. doi: 10.1016/j.gaitpost.2009.07.005. Epub 2009 Jul 25. PMID 19632845
  • Collins JJ, Imhoff TT, Grigg P. Noise-enhanced tactile sensation. Nature. 1996 Oct 31;383(6603):770. doi: 10.1038/383770a0. No abstract available. PMID 8893000

Идентификаторы

NCT: NCT07220707 · 2025-00142

Первоисточники (государственные реестры)

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