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Effect of mahjong game-based upper limb robot training on upper limb function in stroke patients: a functional near-infrared clinical study protocol

Effect of mahjong game-based upper limb robot training on upper limb function in stroke patients: a functional near-infrared clinical study protocol

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084049
Enrollment
Unknown
Registered
2024-05-09
Start date
2024-06-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Stroke

Interventions

Conventional rehabilitation group:The actual sample size will be calculated from the results of the pilot experiment. Subjects in CT group will be treated with clinical pharmacotherapy and conventiona
Traditional robot-assisted training (TRT) group::The actual sample size will be calculated from the results of the pilot experiment. Subjects in TRT group will be treated by clinical pharmacotherapy,
Mahjong game-based upper limb robot-assisted training (MULR) group:The actual sample size will be calculated from the results of the pilot experiment. Subjects in MULR group will accept clinical pharm

Sponsors

West China Hospital of Sichuan Univeristy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with first stroke diagnosed by CT or MRI; 2. Patients within 1 week to 6 months after the onset of stroke; 3. Patients with mild motor dysfunction (Fugl-Meyer Upper-limb score higher than 33 points); 4. The patient has no obvious cognitive dysfunction (MMSE> 21 points); 5. Sitting balance reaches level 2 or above; 6. Age between 40 and 80 years old.

Exclusion criteria

Exclusion criteria: 1. Accompanied by severe heart, lung, liver, kidney disease or other serious diseases; 2. Previous history of seizures or family history of epilepsy; 3. There are implanted metals in the body, such as pacemakers, etc.; 4. Detection of new infarct foci or worsening of secondary bleeding; 5. Severe cervical spine lesions, such as cervical spine instability or spinal stenosis.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment of Upper limb;

Secondary

MeasureTime frame
Montreal Cognitive Assessment, MoCA;Pittsburgh Rehabilitation Participation Scale, PRPS;Modified Barthel Index, MBI;Self-rating Anxiety Scale, SAS;Self-rating Depression Scale, SDS;functional near-infrared imaging assessment;

Countries

China

Contacts

Public ContactXu Yang

West China hospital of Sichuan University

xyprotk@126.com+86 177 8419 8775

Outcome results

None listed

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