Skip to content

Effects of Human-Robot Integration Therapy on Recovery of Hand Dysfunction and Brain Networks in Patients with Post-stroke

Effects of Human-Robot Integration Therapy on Recovery of Hand Dysfunction and Brain Networks in Patients with Post-stroke

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123687
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Stroke

Interventions

Human-Robot Integration Therapy Group, HRIT group:With the assistance of the Flexible Mobile Robot (Medical Device Registration No. 20192191549, Model: RSD RS5, Ruishide, Nanjing, China), therapists c
Robot-Assisted Therapy Group,RAT group:Based on the Brunnstrom selection, the patient completes corresponding grasping therapy programs for the whole hand, three fingers, two fingers, and single finge

Sponsors

Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. patients with first stroke based on the 2019 Chinese diagnostic criteria for major cerebrovascular diseases and neuroimaging confirmation; 2. patients aged 18-80 years within 30 days-180 days; 3. good compliance. Can complete the treatment task; 4. voluntarily signed informed consent; 5. FMA-UE <= 60 points.

Exclusion criteria

Exclusion criteria: 1. Vital signs are unstable; 2. patients suffering from synesthesia, blindness or complete somatosensory loss; 3. severe cardiopulmonary dysfunction; 4. orthopaedic conditions (e.g. fixation contractures, shoulder subluxation and severe arthritis); 5. patients suffering from unilateral spatial neglect with a score of less than 44 on the Star Deletion Test; 6. those with a positive Mini-Cog test or a communication disorder that prevents informed consent or compliance with the study assessment; 7. participation in another clinical trial; 8. patients with mini-strokes; 9. patients who do not require upper limb rehabilitation.

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test,ARAT;

Secondary

MeasureTime frame
Active Range of Motion,AROM;Modified Barthel Index,MBI;Functional Near-Unfrared Spectroscopy;Maximum Grip force;Fugl-Meyer Assessment of Upper Extremity,FMA-UE);Motor Activity Log;

Countries

China

Contacts

Public ContactChen Yong

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

ychen713@163.com+86 27 8424 6337

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026