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Идёт набор NCT07225582

Development of Optimal Sensory Feedback Strategies to Maximize Function After Tetraplegia

Без фазы С лечением Spinal Cord Injury Cervical Spinal Cord Injuries (Complete and Incomplete)

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: Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system.
Кому может быть актуально
Состояния в реестре: Spinal Cord Injury Cervical, Spinal Cord Injuries (Complete and Incomplete). Базовые параметры: 22 лет — 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

Development of Optimal Sensory Feedback Strategies to Maximize Function After Tetraplegia: A Sub-study of the Reconnecting the Hand and Arm to the Brain (ReHAB) Clinical Trial

Обзор

The goal of this clinical trial is to learn more about how stimulating the nerves involved in sensation (either in the limbs or in the brain) can be used to restore sensation in participants who have a spinal cord injury. Participants in this study will have already been enrolled in the "Reconnecting the Hand and Arm to the Brain (ReHAB)" study, and received small electrodes in a part of the brain that is involved in sensing touch and pressure in the hand. The ReHAB study participants will also have received electrodes around the nerves in their arm. In this clinical trial, participants will receive two types of electrical stimulation: * Intracortical microstimulation (ICMS) which involves sending small electrical pulses to the part of the brain that processes sensation. * Peripheral nerve stimulation (PNS) which involves sending small electrical pulses to the nerves in the arm that transmit sensations from the hand. Researchers will try different patterns of stimulation for both ICMS and PNS and study how the participants perceive the sensations from the different stimulation patterns. The researchers will also study how combining ICMS and PNS affects the perceived sensations.

Подробное описание

The overall goal of this study is to compare the sensations that are perceived from intracortical microstimulation (ICMS) to those perceived from peripheral nerve stimulation (PNS), and also to perceived sensations from a combination of ICMS and PNS.

Preceding study

Participants for this study will be individuals with a high-level spinal cord injury who are already enrolled in the "Reconnecting the Hand and Arm to the Brain (ReHAB)" clinical trial (ID# NCT03898804). The ReHAB clinical trial involves receiving tiny electrode arrays in the brain and small electrodes around some of the nerves in the arm. The goal of the ReHAB clinical trial is to restore arm and hand movement and sensation in individuals with paralysis from a spinal cord injury.

Goals of this clinical trial

The purpose of the proposed study is to investigate the perception and functional impact of sensory neurostimulation in participants with tetraplegia. Investigators will develop and implement novel paradigms of ICMS applied to primary somatosensory cortex (S1) and PNS applied to upper extremity nerves through chronically-implanted cuff electrodes. Investigators will also develop and assess hybrid neurostimulation paradigms involving paired application of ICMS and PNS. For each paradigm, investigators will quantify the perceived sensation with classic psychophysical methods. Investigators will also implement the approach into closed-loop tasks in virtual reality controlled through decoded cortical signals recorded from intracortical microelectrode arrays. Finally, investigators will assess the impact of each stimulation paradigm on residual sensory function.

In Aim 1, investigators will develop a novel ICMS paradigm that attempts to reproduce both the temporal and spatial activation patterns that occur in S1 during normal touch. Investigators will compare this novel paradigm to other existing ICMS encoders. Investigators will assess the impact of each ICMS encoder on perceptual response, task performance in virtual reality (VR), and residual sensory function. In Aim 2, investigators will develop novel PNS paradigms and assess the efficacy of PNS for sensory feedback in people with tetraplegia for the first time. As in Aim 1, investigators will develop and compare several PNS encoders, including those that reproduce aspects of the peripheral response to normal touch and traditional linear encoders. We will assess the impact of each PNS encoder on perceptual response, task performance in VR, and residual sensory function. In Aim 3, we will develop hybrid neurostimulation paradigms that pair ICMS with PNS. We will assess the impact of stimulation encoder and stimulation amplitude on the perceived sensations generated by hybrid stimulation. We will then investigate the impact of PNS-ICMS timing delays within the hybrid neurostimulation paradigm on the perceptual response, functional impact, and impact on residual sensory function.

All participants will participate in all aims and will receive all stimulation approaches and perform all tasks and measures. All participants will serve as their own control for the planned statistical analyses. The study will generate tens of thousands of perceptual response data points, hundreds of functional task data points, and hundreds of thousands of intracortical recordings (for exploratory analyses).

Вмешательства

  • Устройство Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system
    Participants with tetraplegia who have received intracortical arrays in the sensory cortex and peripheral nerve cuff electrodes will undergo a variety of stimulation paradigms to investigate the perception and functional impact of sensory neurostimulation.

Первичные конечные точки

  • Force matching success rate [Срок оценки: From enrollment to around two years after enrollment]
  • Object discrimination accuracy [Срок оценки: From enrollment to around two years after enrollment]
  • Discrimination threshold [Срок оценки: From enrollment until around two years post-enrollment]
  • Tactor detection threshold [Срок оценки: From enrollment to around two years after enrollment]
Вторичные конечные точки (7)
  • Sensory dynamic range [Срок оценки: From enrollment until around two years post-enrollment]
  • Projected field location [Срок оценки: From enrollment until around two years post-enrollment]
  • Sensation quality [Срок оценки: From enrollment to around two years after enrollment]
  • Naturalness rating [Срок оценки: From enrollment until around two years post-enrollment]
  • Tactor discrimination threshold [Срок оценки: From enrollment to around two years after enrollment]
  • Force matching time to target [Срок оценки: From enrollment to around two years after enrollment]
  • Posture matching success rate [Срок оценки: From enrollment to around two years after enrollment]

Критерии участия

Критерии включения

  • Enrolled in the ReHAB clinical trial and received ReHAB system components via implantation surgery.
  • Willingness and availability to follow the study protocol.

Критерии исключения

  • Lack of function or operability of all implanted ReHAB system components
  • Severe pain or other chronic medical condition that would prevent the participant from completing study-related activities

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Оценка устройства

Центры проведения

США · 1 центр
  • Case Western Reserve University — Cleveland

Идентификаторы

NCT: NCT07225582 · STUDY20190226 · R01HD117313

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗