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Impact of Multichannel Transcranial direct current stimulation on motor functions in stroke survivors

A Study on Efficacy of Multichannel Transcranial Direct Current Stimulation on Cognitive Domains, Motor Functions of Paretic Hand and Gait in Subacute Stroke Survivors

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022998
Enrollment
60
Registered
2020-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: G968- Other specified disorders of central nervous system

Interventions

Intervention1: Multi channel tDCS: Multi channel (tDCS) +Functional Electrical Stimulation +Saebo Flex+ Conventional Rehabilitation 4 weeks Control Intervention1: Sham Multichannel tDCS: sham Multi

Sponsors

Punjabi University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subacute stroke survivors. 2.Males and females 3.Individuals of the age group (40- Years). 4.Modified Ashworth Scale Score 5.Preserved Range of Wrist Extension (â??10 Degrees). 6.Individuals who are able to walk 7. Individuals with mild cognitive Impairment Mini Mental State Examination (MMSE) Score (18-23). 8.Individuals, who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Individuals diagnosed with hemorrhagic stroke 2.Individuals with a history of neurological disease other than stroke. 3.Individuals with a history of musculoskeletal injury/disease affecting upper Extremity and lower extremity. 4.Individuals with Psychosomatic Illness/ Disease. 5.Individuals with severe cardiovascular & respiratory problem 6.Individuals with uncontrolled hypertension 7.Individuals with any systemic illness. 8.Pregnant women 9.Individuals with metallic Implants. 10.Visual analog scale for pain score >4 in the upper Extremity/lower extremity. 11.Participation in other pharmacological & rehabilitation studies during the study period. 12.Individuals with hypersensitivity or hypoensitivity disorders. 13.Non Cooperative Individuals.

Design outcomes

Primary

MeasureTime frame
Fugl Meyer Assessment Electroencephalography Timepoint: 04 Weeks

Secondary

MeasureTime frame
Montreal Cognitive Assessment Nine Hole Peg Test Grip Strength Pinch Strength Wisconsin gait scale Stroke Specific Quality of Life scale tDCS adverse effect questionnaire Timepoint: 04 Weeks

Countries

India

Contacts

Public ContactNarkeesh Arumugam

Punjabi UNiversity, Patiala

narkeesh@gmail.com9417802662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 16, 2026