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Randomized parallel controlled study: Long-term efficacy of cable-driven upper limb rehabilitation robot control method on motor function recovery after stroke

Randomized parallel controlled study: Long-term efficacy of cable-driven upper limb rehabilitation robot control method on motor function recovery after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119775
Enrollment
Unknown
Registered
2026-03-03
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Stroke

Interventions

ACM group:Cable-driven upper-limb rehabilitation robot-assisted training using an admittance control method.
VCM group:Cable-driven upper-limb rehabilitation robot-assisted training using a variability-encoded control method.
ADFFCM group:Cable-driven upper-limb rehabilitation robot-assisted training using an acceleration distribution based-gradient force field control method

Sponsors

The Seventh Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Stroke patients aged between 18 and 75 years; 2. Time since stroke onset greater than 6 months, with stable clinical condition, in the subacute or chronic phase; 3. Presence of unilateral upper-limb motor impairment, manifested as reduced muscle strength, impaired motor coordination, or limited joint range of motion; hemiplegia affecting regions other than the upper limb was not included; 4. The affected upper limb retains a certain degree of voluntary motor function, making the patient suitable for movement-assisted interventions.

Exclusion criteria

Exclusion criteria: 1. Severe muscle spasticity (Modified Ashworth Scale <= 2); 2. Significant cognitive impairment (e.g., Mini-Mental State Examination score <= 24), resulting in inability to understand instructions, cooperate with training, or provide informed consent; 3. Severe structural impairments of the shoulder joint, such as instability, dislocation, or fractures, making the use of rehabilitation robotic devices unsuitable; 4. Severe cardiovascular, respiratory, or neurological diseases that prevent tolerance of the intensity and frequency of rehabilitation training; 5 Other contraindications, including active fractures, severe spasticity, uncontrolled hypertension, or cardiac arrhythmias.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Upper Limb Motor Function Assessment Scale;

Secondary

MeasureTime frame
movement distributions;movement variability;cortical blood oxygen concentration;

Countries

China

Contacts

Public ContactQiang Lin

The Seventh Affiliated Hospital of Sun Yat-sen University

linqiang@sysush.com+86 189 2249 7674

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026