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A clinical trial to study the effectiveness of transcranial direct current stimulation (A very low current brain stimulation) on upper limb movement control in stroke patients.

Efficacy of transcranial direct current stimulation (tDCS) on upper limb motor control in persons with sub-acute stroke - A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013178
Enrollment
40
Registered
2018-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Cerebrovascular accident (Stroke)

Interventions

Intervention1: Anodal Transcranial Direct Current Stimulation: Anodal Transcranial Direct Current Stimulation Intensity - 2mA, Duration - 30 min per session, 1 session per day,5 days per week for 4 c

Sponsors

D Subramanian
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Medically stable participants 2. Cortical or subcortical area lesion supplied by middle cerebral artery, Anterior cerebral artery, Posterior cerebral artery and confirmed by MRI / CT 3. Early or late subacute stage (1- 6 months) 4. Ischemic or hemorrhagic stroke 5. Arm paresis with Chedoke McMaster Arm Score of 2-6 out of 7 and Hand score of 2-6 out of 7. 6. Recurrent stroke with completely recovered previous stroke.

Exclusion criteria

Exclusion criteria: 1. Major neurological (other than stroke) / neuromuscular / orthopaedic problems 2.Major cognitive deficits 3.History of psychiatric disorders,seizure, migraine within last six months 4. Metal in cranium and other implants (cochlear, cardiac) 5. Skin sensitivity 6. Participants taking medications that could affect brain activity (e.g. epileptic and psychoactive drugs)

Design outcomes

Primary

MeasureTime frame
1. kinematic Analysis ( reach-to-grasp standardized Test Task) 2. Montreal Tonic stretch threshold measure (Spatial zones) 3. Chedoke Arm and Hand Activity Inventory (CAHAI- 7 Version) 4. Action Research Arm Test (ARAT) Timepoint: 0 weeks, 4 weeks and 8 weeks

Secondary

MeasureTime frame
1. Reaching Performance Scale 2. Composite spasticity Index 3. Upper Extremity Subset of Fugl – Meyer Motor Function Assessment (UE –FMA) 4. Patient Health Questionnaire-9Timepoint: 0 weeks, 4 weeks and 8 weeks

Countries

India

Contacts

Public ContactDr John Solomon

School of Physical and Occupational Therapy, McGill university

mindy.levin@mcgill.ca514-398-3994

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026