Actively Recruiting
Investigating the Impact of Afferent Stimulation on Proprioceptive Function in Post-Stroke Rehabilitation
Led by Julio S. Lora Millán · Updated on 2025-07-20
20
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this study is to assess the functionality of a sensory stimulation device that uses mechanical vibrations and low-intensity electrical currents to deliver proprioceptive feedback to stroke patients regarding their movements.
CONDITIONS
Official Title
Investigating the Impact of Afferent Stimulation on Proprioceptive Function in Post-Stroke Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy subjects with no neurological or orthopedic conditions affecting upper limb movement
- No upper limb surgery within the past 6 months for healthy subjects
- Adequate physical condition to perform the study session
- Sufficient cognitive ability to understand and follow experimental procedures
- Stroke survivors with ischemic or hemorrhagic stroke causing upper limb motor impairments
- Chronic stroke condition
- Stroke survivors able to follow instructions and actively participate
- Mini-Mental State Examination (MMSE) score greater than 24
- Fugl-Meyer Motor Assessment upper limb score between 35 and 53 indicating mild-to-moderate impairment
- Upper limb hypertonia score below 3 on the Modified Ashworth Scale
- Signed informed consent to participate voluntarily
You will not qualify if you...
- Acute musculoskeletal disorders
- Peripheral vascular diseases
- Acute cardiopulmonary conditions
- Acute neurological disorders
- Restricted mobility of upper limb joints for any reason
- Pain causing impaired upper limb mobility
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Universidad Rey Juan Carlos
Móstoles, Madrid, Spain, 28933
Actively Recruiting
Research Team
J
Julio S. Lora Millán, PhD in Automation and Robotics
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
2
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