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Harnessing Neuroplasticity to Enhance Functional Recovery During Chronic Recovery From Upper Extremity Nerve Repair
Harnessing Neuroplasticity to Enhance Functional Recovery in Allogeneic Hand Transplant and Heterotopic Hand Replant Recipients
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Individuals whom have received a unilateral allogeneic transplantation proximal to the wrist and are at the chronic stage of recovery (approx. 12 - 18 months following surgery, when Tinel's sign reaches the distal fingertips). * Individuals whom have undergone a complete amputation the hand between the wrist and elbow followed by successful re-attachment and are at the chronic stage of recovery (approx. 12 - 18 months following surgery, when Tinel's sign reaches the distal fingertips). * Individuals whom have undergone repairs of the median, ulnar, or other related or nearby nerve(s) following complex volar forearm lacerations or other injuries between the distal wrist crease and the flexor musculotendinous junctions. Individuals must be at the chronic stage of recovery (approx. 12 - 18 months following surgery, when Tinel's sign reaches the distal fingertips). Exclusion Criteria: * Individuals with significant/severe brain trauma * Serious psychiatric conditions * Chronic or severe neurological conditions. * Current pregnancy * History of seizures or unexplained loss of consciousness * Metallic implants above the chest * Certain implanted medical devices.
About the study
This study adopts a strategy that has arisen from basic neuroscience research on facilitating adaptive brain plasticity and applies this to rehabilitation to improve functional recovery in peripheral nervous system injuries (including hand transplantation, hand replantation, and surgically repaired upper extremity nerve injuries). The technique involves combining behavioral training with transcranial direct current stimulation (tDCS)-a non-invasive form of brain stimulation capable of facilitating adaptive changes in brain organization.
What is being tested
- Transcranial Direct Current Stimulation (device)
- Modified Constraint Induced Movement Therapy (behavioral)
Sponsor: University of Missouri-Columbia · Participants: 180 · Started: Aug 15, 2018
Contact the study team
- Scott H Frey, Ph.D., Ed.M. · Phone: 573-882-4572
Official record on ClinicalTrials.gov — NCT03610763
Locations in the U.S.
| Kentucky | Christine Kleinert Institute for Hand & Microsurgery, Louisville |
| Missouri | University of Missouri, Columbia Washington University School of Medicine, St Louis |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.