Post Stroke Recovery

2

Review clinical trials related to Post Stroke Recovery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Combined Functional Electrical and Transcranial Direct Current Stimulation for Foot Drop

This study aims to determine if combining the treatments of transcranial direct current stimulation (tDCS) and functional electrical stimulation (FES) will better help persons with stroke who have difficulty lifting their toes. As part of the treatment, subjects will receive electrical stimulation through pads on their scalp (similar to what one may have received in physical therapy previously to an arm or leg). This protocol is called transcranial direct current stimulation (tDCS). Subjects will also receive electrical stimulation through pads on their leg. This is called functional electrical stimulation (FES). During treatment sessions, subjects will also perform leg activity/strengthening exercises. The aim is to evaluate whether combining FES and tDCS within a PT session would reduce foot drop as indicated by improvements in the amount of toe clearance and ankle motion persons with stroke.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saint Joseph's University, PhiladelphiaUpdated: May 18, 2026Locations: 1
Eligibility criteria

18 years or older [+3]

An inability to repeat and understand 2-step commands. [+2]

Status: Recruiting

Personalised Health Motor and Cognitive Assistance System for RehAbilitation (PHRASE)

This study is a multicentric randomized controlled trial evaluating the effectiveness of digital technology, specifically a smartphone with integrated VR-and AR-based intervention, for at-home rehabilitation after stroke. The study focuses on combined motor and cognitive training for patients in the late subacute and chronic phases post-stroke. The intervention is provided through the Rehabilitation Gaming System application RGSapp, a goal-oriented, first-person virtual reality (VR) and augmented reality (AR) mobile application for upper limb rehabilitation. A total of seventy participants will be randomly assigned (1:1 ratio) to either the RGSapp intervention or conventional therapy/standard of care for six weeks. The primary outcome is motor function improvement (upper limb), assessed using the Action Research Arm Test (ARAT). Secondary outcomes include changes in cognitive function, depression, usability, adherence, validity of remote assessments, and healthcare costs.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Eodyne Systems SLUpdated: Jan 6, 2026Locations: 2
Eligibility criteria

Patients presenting an ischemic or intracerebral haemorrhagic stroke, ≥ 3 months... [+7]

Presence of a condition or abnormality that, in the opinion of the investigator,... [+3]