The aim of this study is to determine whether a 4-week treatment of repetitive transcranial magnetic stimulation (rTMS) can alleviate the symptoms of neuropathy in individuals with diabetic neuropathy. The study will involve using questionnaires, nerve assessments, sensory tests, blood flow measurements, and blood tests to monitor any changes in symptoms after the rTMS intervention.
Age range
20 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Modified Toronto Clinical Neuropathy Score
Timeframe: Immediately before intervention, immediately following intervention, 4 weeks after intervention
PROMIS-29 v2.0 Profile
Timeframe: Immediately before intervention, immediately following intervention, 4 weeks after intervention
Patient Perceived Global Index of Change (PGIC)
Timeframe: Immediately following intervention, 4 weeks after intervention
Pain catastrophizing scale-EN-SF
Timeframe: Immediately before intervention, immediately following intervention, 4 weeks after intervention