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Comparing the effects of transcranial direct current stimulation (tDCS) as prior and concurrent motor priming combined with mirror therapy on the upper limb motor function recovery in chronic stroke patients: A pilot study

Comparing the effects of transcranial direct current stimulation (tDCS) as prior and concurrent motor priming combined with mirror therapy on the upper limb motor function recovery in chronic stroke patients: A pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020088
Enrollment
Unknown
Registered
2018-12-14
Start date
2018-01-22
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Stroke

Interventions

concurrent-tDCS group:30-min tDCS applied concurrently with 30-min mirror therapy
prior-tDCS group:30-min tDCS applied prior to 30-min mirror therapy
sham-tDCS group:sham-tDCS applied randomly concurrently with or prior to 30-min mirror therapy

Sponsors

The Hong Kong Polytechnic University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
38 Years to 73 Years

Inclusion criteria

Inclusion criteria: 1) Adults (aged = 18 years old) experienced a first stroke for more than 6 months; 2) Upper extremity impairment = 2nd level in Functional Test for the Hemiparetic Upper Extremity (FTHUE)); 3) Medically stable; 4) Mini-mental State Examination (MMSE) = 21, which was to make sure the participant could understand instructions and make consent; 5) Not participating in other clinical, drug or research studies at this moment; 6) Passing the tDCS Adult Safety Screen (TASS).

Exclusion criteria

Exclusion criteria: Those who had severe health conditions that required intensive medicine care such as heart failure, pneumonia, poor nutritional state or contraindications of tDCS like cardiac pacemaker, cancer, bleeding tendency, pregnancy, metal implants, history of seizure, etc. will be excluded.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment-Upper Extremity (FMA-UE);Action Research Arm Test (ARAT);Box and Block Test (BBT);

Countries

China

Contacts

Public ContactMinxia Jin

Shanghai YangZhi Rehabilitation Hospital (Shanghai Sunshine Rehabilitation Center)

jimiyiyi@sina.com+86 15250969338

Outcome results

None listed

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