Paralysis of trunk muscles and the inability to sit upright is one of the major problems facing adults and children with spinal cord injury (SCI). Activity-based locomotor training has resulted in improved trunk control in children with spinal cord injury, though full recovery is not achieved in all children. Transcutaneous spinal stimulation' (TcStim), a stimulation applied over the skin to the sensory nerves and spinal cord, is a promising tool that may further enhance improvements to trunk control. The purpose of this study is to determine the feasibility (can we do it) and safety of Transcutaneous Stimulation (TcStim) in children with SCI to acutely improve sitting upright and when used with activity-based locomotor training (AB-LT). Thus, can we provide this therapy to children and do so safely examining a child's immediate response and cumulative response relative to safety and comfort. Eight participants in this study will sit as best they can with and without the stimulation (i.e. stimulation applied across the skin to the nerves entering the spinal cord and to the spinal cord) and their immediate response (safety, comfort, trunk position) recorded. Then, two participants will receive approximately 40 sessions of activity-based locomotor training in combination with the stimulation. Their cumulative response of stimulation (i.e. safety, comfort, feasibility) across time will be documented. Participation in this study may last up to 3 days for the 8 participants being observed for acute response to stimulation and up to 9 weeks for the participants being observed for cumulative response to training with stimulation. We will monitor the participants throughout the testing and training for their response to the stimulation (i.e. safety) and their comfort.
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Incidence of skin irritation
Timeframe: 1 week for Aim 1, 9 weeks for Aim 2
Faces Pain Scale-Revised (scale 0-10)
Timeframe: 1 week for Aim 1, 9 weeks for Aim 2
Visual Analog Scale (0-10)
Timeframe: 1 week for Aim 1, 9 weeks for Aim 2
Blood pressure
Timeframe: 1 week for Aim 1, 9 weeks for Aim 2
number of requests to stop the stimulation
Timeframe: 1 week for Aim 1, 9 weeks for Aim 2
Angular excursions of trunk during trunk control assessments
Timeframe: 3 days for Aim 1, 9 weeks for Aim 2