Viewing Study NCT05196737



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Last Modification Date: 2024-10-26 @ 2:22 PM
Study NCT ID: NCT05196737
Status: COMPLETED
Last Update Posted: 2023-11-22
First Post: 2021-12-09

Brief Title: DDN in Stroke--COBRE
Sponsor: Medical University of South Carolina
Organization: Medical University of South Carolina

Study Overview

Official Title: Neurophysiological Characterization of Dry Needling in People With Spasticity Due to Stroke--COBRE
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CDN
Brief Summary: The study team is recruiting 20 adults with spasticity due to chronic stroke for a 7 day study over 2 weeks In people with chronic stroke one of the most common and disabling problems is spasticity increased muscle tone or muscle stiffness The purpose of this research study is to examine effects of dry needling on the nervous system pathways between the muscle spinal cord and brain in people with spasticity due to chronic stroke Dry needling is a procedure in which a thin stainless steel needle is inserted into the skin to produce a muscle twitch response It is intended to release a knot in the muscle and relieve pain

The total study duration is 7 visits over 2 weeks There will be 4 visits the first week and 3 visits the second week The first visit will take about 15 hours during which study staff will determine the best placement of electrodes and create a cast of the participants leg to aid them in quickly placing the electrodes on the remainder of the visits The second and fifth visits will last about 35 hours and all other visits will last about 15 hours Dry needling will take place on the fifth visit only During each visit the participant will be asked to participate in examinations of reflexes muscle responses to non-invasive nerve stimulation and leg function
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
5P20GM109040 NIH None httpsreporternihgovquickSearch5P20GM109040