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Clinical Trial Summary

The purpose of this study is to investigate the effectiveness of low-intensity and prolonged vibrotactile sensory stimulation on symptom relieve in fibromyalgia patients.


Clinical Trial Description

The trial will last up to 8 weeks for each subject and includes:

Three weeks treatment 1 (sham or actual) Two week washout Three weeks treatment 2 (sham or actual) Vibrotactile sensory stimulation will consist on whole-body stimulation with mechanical stimuli of pallesthetic type at high rate, low intensity and long daily duration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03227952
Study type Interventional
Source Neurovoxel SLP
Contact
Status Completed
Phase N/A
Start date September 4, 2017
Completion date May 31, 2018

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