Stroke Clinical Trial
— hARMoniesOfficial title:
Association of Dual Transcranial Electrical Stimulation (tDCS) to Upper Limb Robotic Therapy in Individuals With Chronic Stroke
NCT number | NCT03026712 |
Other study ID # | FSLCBM01 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2016 |
Est. completion date | December 1, 2021 |
Verified date | July 2022 |
Source | I.R.C.C.S. Fondazione Santa Lucia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The two cerebral hemispheres find themselves in a state of balanced mutual inhibition. A stroke with involvement of motor function leads to a reduced excitability in affected hemisphere M1 and to an increased excitability of contralateral M1. Stroke therefore might impair interhemispheric balance, leading to a decreased inhibition of contralesional hemisphere by ipsilesional hemisphere and, in turn, to an increased inhibition of ipsilesional hemisphere by contralesional hemisphere. Permanence of healthy hemisphere hyperactivation in chronic phase after stroke is usually index of little functional recovery and is correlated with a greater ipsilateral structural damage. Robot-mediated physical therapy is an innovative rehabilitation technique that is effective in stroke patients. In this study, the investigators will add a non-invasive brain stimulation protocol with Transcranial stimulation with direct current (tDCS) to the robotic treatment in chronic stroke patients. tDCS is a non-invasive brain stimulation technique that is able to modulate cortical excitability. The hypothesis is that dual t-DCS (ipsilesional excitation and concomitant contralesional inhibition) could restore interhemispheric balance improving the benefits of robotic therapy with Armeo Power®.
Status | Completed |
Enrollment | 80 |
Est. completion date | December 1, 2021 |
Est. primary completion date | December 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Subjects with isolated ischemic stroke, confirmed by brain imaging (MRI, CT) - subjects who retain sufficient cognitive functions and language to follow the instructions given by doctors and therapists - subjects with basal Modified Ashworth Scale score under 3 - subjects with basal Fugl-Meyer score = 3 so that they are not completely paralyzed - subjects who have signed informed consent to participate in this study - subjects that show stable conditions in the two pre-treatment evaluations, in order to avoid "Hawthorne effect" Exclusion Criteria: - subjects with chronic paretic limb deformities - subjects with complete and flaccid paralysis of all motor performances of shoulder and elbow; - subjects with severe hemineglect (Pizzamiglio battery for unilateral spatial neglect including letter cancellation test, barrage tests, reading and Wundt-Jastro area illusion test; patients diagnosed with neglect if 3 of 4 items of this battery are present) - subjects showing an increase in the Fugl-Meyer more than 2.1 points in the second pre-treatment clinical evaluation, compared to the score of the first evaluation - subjects with contraindications to the execution of transcranial magnetic stimulation - TMS - (pacemakers, metal implants) - subjects with epilepsy - Previous neurosurgical interventions - Severe upper limb osteoporosis - Upper limb strength or joint movement limitation due to previous fractures - Upper limb strength or joint movement limitation due to previous surgical interventions - Mini Mental State Evaluation (MMSE) <24 |
Country | Name | City | State |
---|---|---|---|
Italy | I.R.C.C.S. Fondazione Santa Lucia | Rome | |
Italy | Policlinico Universitario Campus Bio-Medico | Rome |
Lead Sponsor | Collaborator |
---|---|
I.R.C.C.S. Fondazione Santa Lucia | Campus Bio-Medico University |
Italy,
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* Note: There are 36 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Significant Fugl-Meyer Assessment Upper Extremity (FMA-UE) improvement in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training and at 1 and 3 months follow-up | ||
Secondary | Significant Modified Ashworth scale improvement in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training and at 1 and 3 months follow-up | ||
Secondary | Significant Action Research Arm Test (ARAT) improvement in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training and at 1 and 3 months follow-up | ||
Secondary | Significant Barthel index improvement in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training and at 1 and 3 months follow-up | ||
Secondary | Significant kinematic performance improvement, measured by ArmeoPower®, in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training | ||
Secondary | Significant rebalancing of motor evoked potential (MEP) laterality index in real dual tDCS group vs sham tDCS group | first assessment will occur within 2 days from enrollment, and will be repeated within 2 days from the end of 2 week-training |
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