Clinical Trial

Biofeedback After Stroke

Enrolling by Invitation
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Record status
This record was last updated August 29, 2025 (before its estimated December 2025 completion). Its status may not reflect the trial's current state.
Summary
Studies show that the use of electromyographic biofeedback combined with other therapies contributes to the reduction of upper limb spasticity after stroke. However, there is a lack of literature regarding the best protocols to use in clinical practice, as well as functional outcomes after this therapy. The objective of this research project will be to investigate the effect of electromyographic biofeedback on spasticity in individuals post-stroke in the sub-acute phase, and its outcomes regarding upper limb function and participation in activities of daily living. The study will be a randomized, triple-blind clinical trial in which the 45 participants will be divided into two groups: the experimental group will receive electromyographic biofeedback combined with functional training, and the control group will receive functional training with placebo biofeedback alone. The study hypothesis is that the use of electromyographic biofeedback contributes to improved functional outcomes and participation in activities of daily living in patients with upper limb spasticity resulting from stroke.
Trial Details
NCT Number NCT07149129
Lead Sponsor Universidade Federal do Paraná
Collaborators: UTFPR
Conditions Stroke
Enrollment 45 participants
Start Date 2025-08
Primary Completion 2025-12 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2025-08-29