Health Condition 1: - Health Condition 2: I619- Nontraumatic intracerebral hemorrhage, unspecified
Conditions
Interventions
Intervention1: Experimental Group: TDCS FOR 20 min per session, 5 sessions in a week for 5 weeks.
Control Intervention1: Control Group: Receive a procedure designed to mimic the experimental group in
Sponsors
Prabhat Gupta
Eligibility
Inclusion criteria
Inclusion criteria: Age above 18 year Patients diagnosed with hemiplegia due to ischemic and hemorrhagic stroke unilateral limb paralysis and motor dysfunction of lower limbs MOCA above 22 MAS less than or equal to 3 in the lower limb Both male and female patient Ability to maintain sitting balance independently and stand with or without minimal support Participate voluntarily and sign an informed consent formhe clinical symptoms include unilateral limb paralysis and motor dysfunction of lower limbs Montreal cognitive Assessment Stable state clear consciousness and no hearing and comprehension disabilities to complete the questionnaires Participate voluntarily and sign an informed consent form
Exclusion criteria
Exclusion criteria: MAS less than or equal to 4 Severe cognitive impairement global aphasia or perceptual deficit Tracheostomy patients Patients with serious internal diseases tumors and other malignant diseases infectious diseases and mental illnesses Contraindications for electrical stimulation devices such as with pacemakers or other implantable devices history of epilepsy or and seizures History of head trauma or head and spinal cord surgery bleeding disorders in pregnancy or lactation or planning to become pregnant in the next 6 months injuries swelling or scarring at the skin of the stimulating sites sensory disturbance or allergy to electrical stimulation Have taken muscle relaxant drugs in the past month or have received botulinum toxin injections in a spastic limb within the past 6months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cognition Balance GaitTimepoint: Baseline and 5 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of lifeTimepoint: Baseline and 5 weeks | — |
Countries
India
Contacts
Public ContactDr Saurabh Kumar
sgt university
Outcome results
None listed