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Study identifier: NCT07306104 Synced from ClinicalTrials.gov · July 29, 2026
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The Effect of Long-term Daily Stimulation of the Brain With Pulsed Electromagnetic Fields on Parkinsons Disease

Condition: PARKINSON DISEASE (Disorder)  ·  Sponsor: University of Southern Denmark

PhaseNA
Planned participants90
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The goal of this clinical trial is to learn to what extent daily stimulation of the brain with transcranial pulsed electromagnetic fields (T-PEMF) works to treat persons with Parkinson's Disease. The main questions it aims to answer are: * How does 6 months of daily treatment (30 minutes/day) with T-PEMF affects neuro-mechanical and molecular biological factors compared with placebo treatment in persons with Parkinson's disease? * How does 12 months of daily treatment (30 minutes/day) with T-PEMF affects neuro-mechanical and molecular biological factors in persons with Parkinson's disease an does 12 months of T-PEMF alters the need for medication intake? The neuro-mechanical outcomes are compared with the "natural" progression of the disease as well as with a healthy reference group. Furthermore, it will be examined whether 12 months of T-PEMF treatment alters the need for medication intake. Participants in the intervention group will: * receive one 30 min treatment session daily for 12 months * receive either T-PEMF or sham treatment for the first 6 months * receive active T-PEMF treatment the last 6 months * visit for tests before treatment initiation, after 6 months of treatment and after 12 months of treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Anne Sofie Bøgh Malling, Ph.d.  ·  +45 28903733  ·  amalling@health.sdu.dk

Bente Rona Jensen, Professor  ·  brjensen@health.sdu.dk

Always discuss trial participation with your own doctor first.

Locations (2)

Odense University HospitalOdense, DenmarkRecruiting
University of Southern DenmarkOdense, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT07306104