Stroke Clinical Trials in Washington D.C., District of Columbia

11 studies are recruiting for stroke in Washington D.C., District of Columbia right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.

Search these by distance from you

Studies now recruiting

1. Vision Improvement Through Behavioral Rehabilitation And Neuroplasticity Training

   The VIBRANT (Vision Improvement through Behavioral Rehabilitation And Neuroplasticity Training) study is a prospective, double-blind, crossover design (within-subject) in participants with homonymous hemianopia-a type of visual field loss resulting from damage to the post-chiasmatic visual pathways…

   Stage

   Not phased

   Ages

   18 and older

   Site

   Georgetown University Medical Center, Washington D.C., District of Columbia

   Run by

   Georgetown University

   See if you can join NCT07105358 on ClinicalTrials.gov

2. Home-based Vision Rehabilitation Guided by Brain Imaging

   The BRIGHT (Behavioral Rehabilitation Through Image-Guided Home-based Training) study aims to evaluate the effectiveness of image-guided, home-based perceptual training at improving visual performance in individuals with visual field loss. Using a prospective, crossover design, BRIGHT combines visu…

   Stage

   Not phased

   Ages

   18 and older

   Site

   Georgetown University Medical Center, Washington D.C., District of Columbia

   Run by

   Georgetown University

   See if you can join NCT07635329 on ClinicalTrials.gov

3. Telerehabilitation In The Home After Stroke

   The purpose of this research study is to evaluate whether telerehabilitation targeting arm movement, when added to usual care, improves arm function and reduces global disability after stroke, compared to usual care alone. Patients with arm weakness due to stroke that happened in the past 90-150 da…

   Stage

   Not phased

   Ages

   18 to 80

   Site

   Medstar Health Research Institute, Washington D.C., District of Columbia

   Locations

   27 in total

   Run by

   University of California, Los Angeles

   See if you can join NCT06682429 on ClinicalTrials.gov

4. CoMind Early Feasibility Study

   The purpose of this research, which has been determined as non-significant risk by the central IRB overseeing the study, is to obtain information to help further develop a machine (a medical device) to measure the pressure around the brain from the outside (this pressure is called intracranial pres…

   Stage

   Not phased

   Ages

   18 and older

   Site

   Medstar Health, Washington D.C., District of Columbia

   Locations

   16 in total

   Run by

   CoMind Technologies Limited

   See if you can join NCT06368648 on ClinicalTrials.gov

5. Validation of Early Prognostic Data for Recovery Outcome After Stroke for Future, Higher Yield Trials

   VERIFY will validate biomarkers of upper extremity (UE) motor outcome in the acute ischemic stroke window for immediate use in clinical trials, and explore these biomarkers in acute intracerebral hemorrhage. VERIFY will create the first multicenter, large-scale, prospective dataset of clinical, tra…

   Stage

   Not phased

   Ages

   18 and older

   Site

   MedStar Washington Hospital Center, Washington D.C., District of Columbia

   Locations

   45 in total

   Run by

   Yale University

   See if you can join NCT05338697 on ClinicalTrials.gov

6. Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis- Magnetic Resonance Imaging

   CAPTIVA-MRI is an observational multimodal MR imaging study that is ancillary to the CAPTIVA trial [a 3-arm, double-blind Phase III trial conducted at approximately 115 StrokeNet sites randomizing patients with stroke attributed to 70-99% intracranial atherosclerotic stenosis (ICAS) to aspirin plus…

   Stage

   Not phased

   Ages

   18 and older

   Site

   MedStar Washington Hospital Center, Washington D.C., District of Columbia

   Locations

   28 in total

   Run by

   Yale University

   See if you can join NCT05907629 on ClinicalTrials.gov

7. Assistance Delivery and Muscle Coordination

   The experiment will be conducted with 15 chronic stroke survivors and 15 control subjects. Subjects will perform extension movements of the index finger of their more-impaired (stroke) or nondominant (control) hand under two different assistance types: end-effector assistance and exotendon assistan…

   Stage

   EARLY_Phase 1

   Ages

   20 to 80

   Site

   Catholic University of America, Washington D.C., District of Columbia

   Run by

   The Catholic University of America

   See if you can join NCT07011173 on ClinicalTrials.gov

8. Anticoagulation for New-Onset Post-Operative Atrial Fibrillation After CABG

   The primary objective of this study is to evaluate the effectiveness (prevention of thromboembolic events) and safety (major bleeding) of adding oral anticoagulation (OAC) to background antiplatelet therapy in patients who develop new-onset post-operative atrial fibrillation (POAF) after isolated c…

   Stage

   Phase 3

   Ages

   18 and older

   Site

   MedStar Washington Hospital Center, Washington D.C., District of Columbia

   Locations

   106 in total

   Run by

   Icahn School of Medicine at Mount Sinai

   See if you can join NCT04045665 on ClinicalTrials.gov

9. Sensory Feedback and Hand Motor Adaptation

   The following experiment will be conducted with 15 chronic stroke survivors and 15 control subjects. Subjects will perform hand movements in the virtual reality environment using a head-mounted display. Quest's onboard cameras allow real-time tracking of hand motion, estimating joint angles of the …

   Stage

   EARLY_Phase 1

   Ages

   20 to 70

   Site

   Catholic University of America, Washington D.C., District of Columbia

   Run by

   The Catholic University of America

   See if you can join NCT07598695 on ClinicalTrials.gov

10. Hand Exoskeleton Training Study

    The goal of this study is to evaluate the HandMATE device's effectiveness in the rehabilitation of stroke patients and asses if the HandMATE application is received well by stroke survivors. Participants will use the HandMate device in clinic and in the home. They will also complete clinical upper …

    Stage

    Not phased

    Ages

    21 and older

    Site

    MedStar National Rehabilitation Hospital, Washington D.C., District of Columbia

    Run by

    Medstar Health Research Institute

    See if you can join NCT06786858 on ClinicalTrials.gov

11. ReadMap: Reading in Stroke Alexia and Typical Aging

    Loss of reading ability due to stroke, called alexia, likely affects over a million Americans at any given time and causes difficulty performing many daily life functions, such as paying bills, using email/text, reading for pleasure, and reading signs in the community. Understanding the brain and c…

    Stage

    Not phased

    Ages

    18 and older

    Site

    Georgetown University Medical Center, Washington D.C., District of Columbia

    Run by

    Georgetown University

    See if you can join NCT06700005 on ClinicalTrials.gov