Wireless Nerve Stimulation Device To Enhance Recovery After Stroke
Last updated on July 2021Recruitment
- Recruitment Status
- Not yet recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Chronic Stroke
- Ischemic Stroke
- Stroke
- Upper Extremity Paresis
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Crossover AssignmentIntervention Model Description: Prospective, double blind, randomized placebo controlled, plus open-label extensionMasking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Device Feasibility
Participation Requirements
- Age
- Between 22 years and 79 years
- Gender
- Both males and females
Description
Not Provided
Not Provided
Tracking Information
- NCT #
- NCT04534556
- Collaborators
- The University of Texas at Dallas
- University of Texas Southwestern Medical Center
- National Institute of Neurological Disorders and Stroke (NINDS)
- Investigators
- Principal Investigator: Michael Kilgard, PhD University of Texas at Dallas Principal Investigator: Robert Rennaker, PhD University of Texas at Dallas Study Director: Seth Hays, PhD University of Texas at Dallas Principal Investigator: Jane Wigginton, MD University of Texas Southwestern Medical Center Principal Investigator: Rita Hamilton, DO Baylor Scott & White Institute for Rehabilitation Study Director: Michael Foreman, MD, FACS Baylor Health Care System Study Director: Richard Naftalis, MD, FAANS, FACS Baylor Health Care System Study Director: Mark Powers, PhD Baylor Health Care System Study Director: Ann Marie Warren, PhD Baylor Health Care System
Get Well Soon