Ignite Creation Date:
2024-10-25 @ 7:58 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06541015
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-02
Brief Title:
Effect of Transcutaneous Electrical Nerve Stimulation on Post-stroke Patients
Sponsor:
None
Organization:
None
Study Overview
Official Title:
TENS Transcutaneous Electrical Nerve Stimulation Effect of Transcutaneous Spinal Direct Current Stimulation on Lower Limb Reflex Volitional and Functional Movement Post-stroke
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
TENS
Brief Summary:
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
Detailed Description:
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 During the first session the subjects will be screened and informed about the research study so they can consent to their participation They will also be oriented to the lab the equipment as well as the research team Following the orientation the remaining time will consist of approximately 3 hours of data collection The remaining will last approximately 3 hours and consist of the completion of data collection Additional sessions after 15 sessions will be optional and will be reserved for completing data collection if the subject is unable to complete a trial session or to analyze for test retest variability within the subject population 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None