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High-definition Transcranial Direct Current Stimulation for Facilitating Hand Function Recovery After Stroke

Using Neuroimage and Computational Modeling to Customize High-definition Transcranial Direct Current Stimulation Protocols for Facilitating Hand Function Recovery After Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03875677
Enrollment
25
Registered
2019-03-15
Start date
2019-04-10
Completion date
2020-06-01
Last updated
2021-09-13

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

Conditions

Stroke

Brief summary

Transcranial direct current stimulation (tDCS) had recently been shown having feasibility in modulating cortical excitability transiently during motor training in a noninvasive way. The findings support that tDCS and motor practice can positively promote post-stroke motor learning to improve upper-limb motor recovery after stroke. A randomized controlled trial will be conducted with three groups: HD-tDCS, conventional tDCS and sham HD-tDCS. A 10-session training will be provided to evaluate the effectiveness of transient modulation of cortical excitability through tDCS with clinical assessment scores.

Interventions

DEVICEHD-tDCS group

5 sintered Ag/AgCl ring electrodes will be used at a radius of \ 5cm. The electrodes will be placed inside plastic electrode holders which will be filled with gel to have better contact with the scalp.

DEVICEConventional tDCS group

A pair of 25 cm2 rubber electrodes enclosed in saline-soaked sponges and affixed to the head with rubber bands.

DEVICESham HD-tDCS group

A pair of 25 cm2 rubber electrodes enclosed in saline-soaked sponges and affixed to the head with rubber bands.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Hemiparesis subsequent to first-ever unilateral stroke for more than 6 months; 2. MCP and PIP finger joints can be extended to 180° passively; 3. Sufficient cognition to follow the experimental instructions

Exclusion criteria

1. Severe hand spasticity or hand deformity; 2. History of alcohol or drug abuse or epilepsy; 3. Bilateral brain infarcts; 4. Severe cognitive deficits; 5. Comprehensive aphasia; 6. Contraindications to tDCS

Design outcomes

Primary

MeasureTime frameDescription
Action Research Arm Test (ARAT)3-month after the 10th session trainingThe ARAT has total 19 items, divided into 4 categories (grasp, grip, pinch, and gross arm movement). It ranges from 3 to 0 (best to worse).

Secondary

MeasureTime frameDescription
Fugl-Meyer Assessment (Upper Extremity)3-month after the 10th session trainingThe maximum score is 66, divided into 33 items in the form of a 3-point scale (0-2), 0 is cannot perform and 2 performs fully.
Wolf Motor Function Test (WMFT)3-month after the 10th session trainingThe WMFT measures upper limb ability through timed and functional tasks. It has 17 items, ranging from 0 to 5 (worse to best).
Magnetic Resonance ImagingBaselineFunctional magnetic resonance imaging

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026