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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04586777
Other study ID # 44067
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date January 15, 2014
Est. completion date January 8, 2021

Study information

Verified date January 2021
Source University of Kentucky
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate the effects of non-invasive stimulation of the spinal cord in people with spinal cord injury.


Description:

This study will use a non-invasive form of spinal stimulation, called transvertebral direct current stimulation, or tvDCS. It currently is not clear what effects this type of stimulation has on the excitability of the brain and spinal cord in people with spinal cord injury. In this study, subjects will participate in 3 sessions, with at least 1 week in between sessions, during which they will get a different condition of tvDCS. We will test the excitability of the brain and spinal cord before and after tvDCS in each session.


Recruitment information / eligibility

Status Terminated
Enrollment 27
Est. completion date January 8, 2021
Est. primary completion date January 8, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18 to 65 years of age - Motor incomplete spinal cord injury classified as B, C, or D by the American Spinal Injury Association Impairment Scale (AIS) - More than 12 months post-injury - Lesion at of above thoracic level T8 - Body mass index <30 (in order to facilitate reliable location of body landmarks guiding stimulation) - Severe gait deficit Exclusion Criteria: - Unstable cardiopulmonary conditions - History of seizure, head injury with loss of consciousness, severe alcohol or drug abuse, and/or psychiatric illness - Cognitive deficits severe enough to preclude informed consent - Positive pregnancy test of being of childbearing age and not using appropriate contraception - Ferromagnetic material in the brain or in the spine (except for titanium for segmental fixation of the spine) - Cardiac or neural pacemakers - Fixed contractures in the lower extremities - Uncontrolled diabetes - Severe osteoporosis - Severe spasticity - Decubitus ulcers which interfere with harness support or walking - Severe orthostatic hypotension

Study Design


Intervention

Device:
transvertebral direct current stimulation (tvDCS)
tvDCS is a painless, non-invasive form of spinal stimulation which delivers safe, low levels of electrical current to the spinal cord through the back. It is believed to be able to influence the excitability of the brain and spinal cord.

Locations

Country Name City State
United States University of Kentucky at Cardinal Hill Rehabilitation Hospital Lexington Kentucky

Sponsors (1)

Lead Sponsor Collaborator
University of Kentucky

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in corticospinal excitability This will be measured using transcranial magnetic stimulation to evoke responses in muscles of the lower leg. Immediately before tvDCS, Immediately after tvDCS
Primary Change in spinal cord excitability Hoffmann's reflex will be used to assess spinal cord excitability. For this text, pulses of electrical stimulation will be applied to the back of the knee and the response will be measured from the calf muscle. Immediately before tvDCS, Immediately after tvDCS
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