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Effectiveness of Intelligent Rehabilitation Robot Training System Combined With Repetitive Facilitative Exercise on Upper Limb Motor Function After Stroke: a Randomized Control Trial.

Not Applicable
Completed
Conditions
Stroke
Interventions
Other: repetitive facilitative exercise
Device: intelligent rehabilitation robot training system
Other: conventional therapy
Registration Number
NCT06435624
Lead Sponsor
Nanjing Mingzhou Rehabilitation Hospital
Brief Summary

The goal of this clinical trial is to learn if intelligent rehabilitation robot training system combined with repetitive facilitative exercise (RFE) work to treat stroke in adults. The main questions it aims to answer are:

Does drug intelligent rehabilitation robot training system combined with RFE improve the upper limb motor function of participants? Can the combination of intelligent rehabilitation robot training system and RFE achieve better effects?

Researchers will compare 3 groups (RFE, intelligent rehabilitation robot training system under RFE, and conventional therapy) to see if intelligent rehabilitation robot training system and RFE works to treat stroke.

Participants will:

Receive treatment for 4 weeks Receive scale and instrument testing before and after treatment

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
81
Inclusion Criteria
  • patients (18 to 74 years old) who suffered a first or second unilateral stroke
  • chronic stroke (over 6 months from the onset)
  • obvious upper limb movement disorders (FMA-UE scores from 25 to 42)
  • ability to understand and follow simple directions
Exclusion Criteria
  • pregnant or lactating
  • upper extremity contracture, pain, or trauma
  • perceptual, apraxic, or cognitive deficits that lead to inability to follow verbal instructions
  • unable to maintain sitting posture
  • cerebellar lesion
  • clinically unstable medical disorders
  • inability to provide informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RFE grouprepetitive facilitative exerciseRepetitive facilitative exercise (RFE)
Combined groupintelligent rehabilitation robot training systemIntelligent rehabilitation robot training system under repetitive facilitative exercise (RFE)
CT groupconventional therapyConventional therapy (CT)
Combined grouprepetitive facilitative exerciseIntelligent rehabilitation robot training system under repetitive facilitative exercise (RFE)
Primary Outcome Measures
NameTimeMethod
Fugl-Meyer Assessment for Upper Extremity (FMA-UE)From enrollment to the end of treatment at 4 weeks

The FMA-UE consists of 33 items across nine components, including reflex action, synergy, and coordination, with a maximum score of 66 points. Each items is scored from 0 (no ability) to 2 (full ability), with higher scores indicating better upper limb motor function.

Active Participation ProportionFrom enrollment to the end of treatment at 4 weeks

Active Participation Proportion (APP) is measured using the benchmark evaluation system within the intelligent rehabilitation robot training system. The robotic arm's mechanical sensor continuously detects the force exerted by the patient during the test game and quantifies APP as the ratio of the patient's applied force to the total force required to complete the task (%). A higher APP indicates greater voluntary effort in movement execution. Since the test game difficulty is fixed, APP increases as the patient's motor ability improves.

Trajectory DeviationFrom enrollment to the end of treatment at 4 weeks

Trajectory Deviation (TD) is assessed by comparing the actual motion trajectory with a predefined reference trajectory using the intelligent rehabilitation robot training system. TD is calculated as the mean Euclidean distance (in mm) between discrete points along the actual movement path and the nearest corresponding points on the reference trajectory. This metric provides a measure of point-specific accuracy and precision in following the ideal movement path, with smaller TD values indicating better trajectory control.

Trajectory Tracking ErrorFrom enrollment to the end of treatment at 4 weeks

Description:

Trajectory Tracking Error (TTE) quantifies the cumulative deviation between the actual movement path and the predefined reference trajectory. It is computed as the sum of absolute differences in trajectory length between the two paths (in mm). TTE reflects overall movement efficiency and smoothness, capturing the patient's ability to maintain an optimal movement path throughout the task. A lower TTE indicates better movement planning and motor control.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Nanjing Mingzhou Rehabilitation Hospital

🇨🇳

Nanjing, Jiangsu, China

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