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Clinical study on rewarding occupational therapy combined with tDCS to promote the rehabilitation motivation of stroke patients

Clinical study on rewarding occupational therapy combined with tDCS to promote the rehabilitation motivation of stroke patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090224
Enrollment
Unknown
Registered
2024-09-26
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Stroke

Interventions

tDCS + Reward-based Occupational Therapy Group :1.(tDCS) VC-8000F (), 1.5mA, 5cm×7cm, F3 F7 dlPFC ( 10-20 ),().. 1 , 20min, 15 , 3 . 2. OT brunnstrom ,41,3tDCS ,, 20 , 5 ,3 15 . 21 .3 21 ,.brunstr
Sham Stimulation + Reward-based Occupational Therapy (OT) Group :Sham Stimulation + Reward-based Occupational Therapy
Sham Stimulation + Routine Occupational Therapy (OT) Group :Sham Stimulation + Routine Occupational Therapy

Sponsors

Yueyang Hospital of Intergrated Tradition Chinese and Western Medicine Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Patients diagnosed with stroke by clinical evaluation and comprehensive imaging examination 2. Age =18 and = 80 years old, gender is not limited, right-handed; 3. No cognitive impairment or communication disorder, with a score of 26 or more on the Mini-Mental State Examination (MMSE); First onset; Course of disease =6 months 4 Brunnstrom stage I-VI; 5. Can endure the evaluation process for half an hour to an hour; 6. The subject and his legal guardian understand and agree to participate in this study and jointly sign the informed consent form; 7. The subject's recovery motivation rating scale is below 25 points; 8. The score of the Subjective Indifference Assessment Scale - Clinical Clinician Version is =35 points.

Exclusion criteria

Exclusion criteria: 1. Patients with severe systemic diseases such as cardiopulmonary diseases who are unable to tolerate rehabilitation therapy 2. Patients with confirmed mental illness, severe depression (with suicidal tendencies), epilepsy, or a family history of mental illness or epilepsy 3. The presence of severe systemic diseases such as diabetes and uremia 4. Severe joint contracture 5. Suffering from consciousness disturbance caused by any reason 6. According to safety guidelines, there are contraindications for transcranial direct current/magnetic stimulation (TMS/tDCS) and functional magnetic resonance imaging (fMRI) examinations, such as metal foreign bodies or other implanted electronic devices in the body 7. Auditory or visual impairments that may affect assessment and treatment 8. Using drugs that alter cortical excitability (antiepileptic drugs, sedatives, hypnotics, etc.) 9. Significant pain, sleep disturbances, and mental disorders

Design outcomes

Primary

MeasureTime frame
Rehabilitation Motivation Scale ;

Secondary

MeasureTime frame
Apathy Evaluation Scale, Clinician Version ;Active Rehabilitation Efficacy Ratio ;Fugl-Meyer upper limb assessment ;Function Independent Measure ;ICF-based Activities and Participation Assessment Scale ;fNIRS;fMRI ;STEF;

Countries

China

Contacts

Public ContactDongsheng Xu; Wenxi Li

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai

liwenxi2012@126.com+86 159 2104 5260

Outcome results

None listed

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