Effect of Transcutaneous Electrical Nerve Stimulation on Post-stroke Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of Texas Southwestern Medical Center

About this trial

The subjects will be asked to attend minimum 15 separate sessions, 6 for testing changes in reflex behaviors, 3 for testing changes in the influence of descending motor tracts on spinal motor neurons, 3 for each testing functional movement in response to a trip event and cross-tilt walking adaptation pattern, as part of their participation in the research study. The estimated amount of time to enroll and collect the data for each of the subjects is four months' time. The data will be analyzed and ready for grant preparation (if successful) in approximately four months after the start of the study.

Eligibility criteria

Qualifiers

History of single unilateral stroke with subsequent lower limb hemiparesis on either side (> 6 months since onset)

Ability to walk as part of activities of daily living

Age between 18 and 80

Disqualifiers

Presence of concurrent severe medical illness including unhealed pressure sore, active or untreated infection, thromboembolic disease, severe contracture, osteoporosis, heterotropic classification, lower limb fracture, severe pulmonary disease or cardiovascular instability, uncontrolled seizure, uncontrolled diabetes

History of any neurological injury other than a single stroke

Has received a Botox injection in the lower extremity within the last 4 months

Any cognitive deficit that would prevent informed consent or ability to perform the experiment

Trial design

Treatments tested in this trial

  • InTENSity 10 TENS Stimulator

Treatment groups

100 Participants
are divided into 1 treatment group