Neuromuscular training following concussion: a feasibility study using a virtual platform
During Phase 1 of this study, we will enroll at least n=40 total subjects who are healthy individuals. Subjects will be randomized to one of two study groups and followed throughout the duration of the 8-week NMT intervention period (Figure 3). This study will focus on the assessment of healthy individuals between the ages of 18-40. We will review any and all adverse events as a research team to determine the best course of action should an adverse event occur. For Phase 2 of this study, we will enroll at least n=30 total subjects who are healthy individuals to be tested only at a singular initial visit (Figure 3). This phase of the study will not include randomization or any form of follow-up. This study will focus on the one-time assessment of healthy individuals between the ages of 18-40. We will review all adverse events as a research team to determine the best course of action should an adverse event occur.
MoreAdult
Phase 1 Inclusion criteria consist of being 18-40 years of age at the time of enrollment and report being uninjured and physically able at the time of enrollment. Exclusion criteria consist of having a pre-existing neurological disorder, lower extremity injury at the time of enrollment, or a physician diagnosed concussion <6 months before enrollment. Phase 2 Inclusion criteria consist of being 18-40 years of age at the time of enrollment, report a history of concussion >6 months and <3 years at time of enrollment, and report being uninjured and physically able at the time of enrollment. Exclusion criteria consist of having a pre-existing neurological disorder, lower extremity injury at the time of enrollment, or a physician diagnosed concussion <6 months before enrollment.
Outcomes Research
Department Specific Free Standing Clinic
David Howell, PhD
Protocol Number: 20-3169
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