Auxilium Vitae Rehabilitation Centre
Volterra, 56048, Italy
NCT Number: NCT02496026
The objective of the study is to evaluate the effectiveness of transcranial direct current stimulation (tDCS) integrated with wrist robot-assisted treatment. In detail, the anodal stimulation on the impaired hemisphere will be used associated with a robotic treatment.
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Notify Me18 year–79 year
All sexes
Interventional
Not applicable
Volterra, 56048, Italy
As for transcranial direct current stimulation a HDC kit (ATES/EB NEURO, Firenze, Italy) will be used as device. It is a new device generation of stimulator able to provide an effective stimulation pattern.
As robotic device the InMotion wrist robot (Interactive Motion Technologies Inc., Watertown, MA, USA) will be used. It is an end-effector robotic device able to assist as needed the wrist movements.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients receive robotic rehabilitation session while tDCS stimulator is switched on
Patients receive robotic rehabilitation session while tDCS stimulator is switched off.
Time frame: 6 weeks
Impairment level measure according to ICF
Time frame: 6 months
Impairment level measure according to ICF
Time frame: 6 weeks
Impairment level measure according to ICF
Time frame: 6 months
Impairment level measure according to ICF
Time frame: 6 weeks
Impairment level measure according to ICF
Time frame: 6 months
Impairment level measure according to ICF
Time frame: 6 weeks
Activities level measure according to ICF
Time frame: 6 months
Activities level measure according to ICF
Auxilium Vitae Volterra
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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