Actively Recruiting
Non-invasive Neuromodulation NESA Application in the Rehabilitation of Stroke Sequelae
Led by University of Las Palmas de Gran Canaria · Updated on 2026-05-05
30
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate whether NESA microcurrents can be used as an effective treatment for various sequelae present in stroke patients, specifically in the treatment of spasticity, balance, pain; and whether it affects quality of life, performance of activities of daily living and quality of sleep.
CONDITIONS
Official Title
Non-invasive Neuromodulation NESA Application in the Rehabilitation of Stroke Sequelae
Who Can Participate
Eligibility Criteria
You may qualify if you...
- People who have suffered a stroke with an evolution between 6 months and 6 years.
- Optimal cognitive capacity and mentally competent to participate in the study and complete the required questionnaires.
- People able of standing upright, including those who need technical aids.
You will not qualify if you...
- Present some of the contraindications for a treatment with NESA XSIGNAL: pacemakers, internal bleeding, not to apply electrodes on skin in bad condition, with ulcerations or wounds, acute febrile processes, acute thrombophlebitis and/or phobia to electricity.
- Not having signed the informed consent form.
- Presenting any additional injury or pathology during the study.
- Not having the optimal cognitive capacities for understanding and participating in the study.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mariola Lledó Amat
Las Palmas de Gran Canaria, Las Palmas, Spain, 35016
Actively Recruiting
Research Team
M
Mariola Lledó Amat, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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