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Clinical Research Directory

Browse clinical research sites, groups, and studies.

5 clinical studies listed.

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Stroke, Cardiovascular

Tundra lists 5 Stroke, Cardiovascular clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT06911671

EMG Control Assistance Virtual Reality Interface Coupled With Cerebellar-iTBS for Arm Recovery After Stroke (ERICA)

The investigators hypothesize that a myoelectric (EMG) controlled virtual reality (VR) interface allows for effective upper limb motor recovery of stroke patients. EMG control offers the possibility to alter visual feedback according to the recorded muscle activity in real-time. By manipulating the motion of a virtual hand associated with the recorded muscle patterns, assistance can be provided to stroke patients by correcting the error between the actual (dysfunctional) and a reference (functional) muscle pattern. Thus, through such an assistive EMG control algorithm, patients will be able to perform reaching movements with the virtual hand despite their motor impairment. By gradually reducing assistance, it is hypothesized that the salient error in the task space provided as visual feedback will systematically change the muscle patterns, thereby driving adaptation of the dysfunctional muscle patterns, enhancing motor recovery. Moreover, due to its relevant role in motor learning, it is expected that cerebellar stimulation will favor the underlying processes of adapting cerebello-cortical plasticity involved in motor learning. Therefore, it is hypothesized that an assistive EMG control algorithm in combination with cerebellar transcranial magnetic stimulation will further enhance upper limb recovery.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2026-02-03

1 state

Stroke
Stroke, Cardiovascular
RECRUITING

NCT06569121

Efficacy of a Telehealth Delivered Group Lifestyle Balance for People Post Stroke (tGLB-CVA)

Investigators will conduct a randomized controlled trial (RCT) to assess intervention efficacy of telehealth delivery of the GLB-CVA (tGLB-CVA) compared to a 6-month wait-list control (WLC) in partnership with a diverse group of patient partners and peer mentors.

Gender: All

Ages: 18 Years - 85 Years

Updated: 2026-01-21

1 state

Stroke, Acute
Stroke
Stroke, Cardiovascular
+2
RECRUITING

NCT06483230

Implementation of IVS3 for Upper Limb Motor Recovery

This study measures participant satisfaction and upper extremity function in outpatients with chronic stroke when exposed to the IVS3 device. Investigators hypothesize that treatment with the IVS3 device will be feasible and tolerable for use in the outpatient setting.

Gender: All

Ages: 18 Years - Any

Updated: 2025-10-29

1 state

Neglect, Hemispatial
Stroke, Cardiovascular
Mirror Movement
+1
RECRUITING

NCT04038697

Ischemic Conditioning Improves Walking Function Post Stroke

This innovative study will address scientific and clinical areas relatively unexplored in chronic stroke that could lead to greater recovery of walking. Ischemic Conditioning (IC) is a non-invasive, simple procedure that improves motor function, exercise performance and cardiovascular function in healthy controls, but it has never been applied to the stroke population. We postulate that IC enhances the recruitment of motoneurons and results in positive neural adaptations, improves vascular endothelial function and peripheral blood flow, and together these improvements result in an increased capacity to exercise and faster walking speed. Future studies will examine the effects of IC and traditional therapy at different time points of recovery post stroke, durability of IC, molecular mechanisms of neural and cardiovascular adaptation and the efficacy compared with other adjuncts.

Gender: All

Ages: 18 Years - 85 Years

Updated: 2025-04-25

1 state

Stroke
Stroke, Ischemic
Stroke Hemorrhagic
+1
NOT YET RECRUITING

NCT05046106

MLC1501 Study Assessing Efficacy in STROke Recovery

This is a multi-center, randomized, double-blind, placebo-controlled, dose-response study of MLC1501 in patients with stroke. Eligible participants will be randomized in a 1:1:1 ratio to orally receive MLC1501 low-dose twice a day, MLC1501 high-dose twice a day, or matching placebo for 24 weeks.

Gender: All

Ages: 18 Years - Any

Updated: 2023-03-16

Stroke
Stroke, Ischemic
Strokes Thrombotic
+4