Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Stroke Hemorrhagic
  • Stroke Ischemic
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: The present study will be conducted in over 15 recruiting centers with a randomized double-blind design. Post-stroke patients will be randomly assigned to 3 parallel groups: Control Group (neuromotor training and sham stimulation), Experimental Group 1 (neuromotor training and cathodal tDCS over the unaffected hemisphere), Group 2 (neuromotor training and anodal tDCS over the affected hemisphere). Participants will be further partitioned on the basis of the acute/subacute and subacute/chronic stages (7-90 and 91 days from lesion onset, respectively).Masking: Double (Participant, Outcomes Assessor)Masking Description: Both participants and experimenters will be prevented from having knowledge of the assigned stimulation protocol. To do so, the investigator will create a series of numbers paired with real and sham interventions while the outcome assessor will be aware of the patient-number association only.Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 90 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04166968
Collaborators
  • Azienda Unità Sanitaria Locale di Piacenza
  • San Gerardo Hospital
  • Maggiore Bellaria Hospital, Bologna
  • Azienda Ospedaliero, Universitaria Pisana
  • Fondazione Don Carlo Gnocchi Onlus
  • Azienda Ospedaliera Universitaria Integrata Verona
  • Azienda Ospedaliero Universitaria di Cagliari
  • Ospedale Policlinico San Martino
  • I.R.C.C.S. Fondazione Santa Lucia
  • Catholic University of the Sacred Heart
  • Istituti Clinici Zucchi
  • Ospedali Riuniti di Foggia
Investigators
Principal Investigator: Carlo Miniussi, PhD IRCCS Centro San Giovanni di Dio Fatebenefratelli