Chronic Stroke Clinical Trial
Official title:
A Wearable for Post-stroke Rehabilitative Multi-muscle Stimulation Inspired by the Natural Organization of Neuromuscular Control
Participants are seeking to unleash the full therapeutic potential of a newly developed, customizable and potentially commericializable 10-channel Functional Electrical Stimulation (FES) to rehabilitate the gait of chronic stroke survivors. Each subject will undergo 18-sessions (~1 month) FES training. Participants will utilize the theory of muscle synergies from motor neurosciences, which are defined as neural modules of motor control that coordinate the spatiotemporal activation patterns of multiple muscles, to guide our personal selections of muscles for FES. It is hypothesized that chronic stroke survivors will learn from FES stimulations, over several daily sessions, both by suppressing the original abnormal muscle synergies and by employing the normal muscle synergies as specified in the FES. It is also expected that the walk synergies of the paretic side of chronic stroke survivors should be more similar to healthy muscle synergies at the two post-training time points than before training.
Status | Recruiting |
Enrollment | 45 |
Est. completion date | June 23, 2024 |
Est. primary completion date | March 23, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 85 Years |
Eligibility | Inclusion Criteria: 1. Right-handed elderly chronic stroke survivors; age =40; =6 months post-stroke 2. Unilateral ischemic brain lesions 3. Participants should be able to walk continuously for =15 min. with or without assistive aid Exclusion Criteria: 1. Cannot comprehend and follow instructions, or with a score <21 on the mini-mental state exam; 2. Have cardiac pacemaker; 3. Have skin lesions at the locations where FES or EMG electrodes may be attached; 4. Have major depression; 5. Present with severe neglect 6. Patients with type i and ii diabetes |
Country | Name | City | State |
---|---|---|---|
Hong Kong | The Hong Kong Polytechnic University | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong | City University of Hong Kong, Shanghai Jiao Tong University School of Medicine, The Hong Kong Polytechnic University |
Hong Kong,
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* Note: There are 61 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Surface electromyographic signals from up to 14 muscles on the paretic and non-paretic side during gait. | To assess the muscle synergies, surface EMGs will be recorded from 14 muscles (tibialis anterior (TA), medical gastrocnemius (MG), soleus (SOL), vastus medialis (VM), rectus femoris (RF), hamstrings (HAM), adductor longus (AL), gluteus maximus (GM) lateral gastrocnemius (LG), vastus lateralis (VL), tensor fasciae latae (TFL), erector spinae (ES), external oblique (EO), and latissimus dorsi (LatDor)), using a wireless EMG system (Delsys; 2000 Hz). All electrodes will be securely attached to skin surface using double-sided and medical tapes. | The assessment will be performed at baseline | |
Primary | Surface electromyographic signals from up to 14 muscles on the paretic and non-paretic side during gait. | To assess the muscle synergies, surface EMGs will be recorded from 14 muscles (tibialis anterior (TA), medical gastrocnemius (MG), soleus (SOL), vastus medialis (VM), rectus femoris (RF), hamstrings (HAM), adductor longus (AL), gluteus maximus (GM) lateral gastrocnemius (LG), vastus lateralis (VL), tensor fasciae latae (TFL), erector spinae (ES), external oblique (EO), and latissimus dorsi (LatDor)), using a wireless EMG system (Delsys; 2000 Hz). All electrodes will be securely attached to skin surface using double-sided and medical tapes. | The assessment will be performed at 5.5 weeks | |
Primary | Surface electromyographic signals from up to 14 muscles on the paretic and non-paretic side during gait. | To assess the muscle synergies, surface EMGs will be recorded from 14 muscles (tibialis anterior (TA), medical gastrocnemius (MG), soleus (SOL), vastus medialis (VM), rectus femoris (RF), hamstrings (HAM), adductor longus (AL), gluteus maximus (GM) lateral gastrocnemius (LG), vastus lateralis (VL), tensor fasciae latae (TFL), erector spinae (ES), external oblique (EO), and latissimus dorsi (LatDor)), using a wireless EMG system (Delsys; 2000 Hz). All electrodes will be securely attached to skin surface using double-sided and medical tapes. | The assessment will be performed at 2.5 weeks | |
Secondary | Gait kinemetics | During FES sessions, kinematic measurements will be provided by the wearable's IMUs. During sessions of motor-impairment assessments, we will capture more precise kinematics using a 10-camera motion capture system (VICON; 200 Hz). This system tracks the 3D positions of 40 markers placed on the legs and torso, and is equipped with suitable models for reconstructing bilateral angles of the hip, knee and ankle. | The assessment will be performed at baseline | |
Secondary | Gait kinemetics | During FES sessions, kinematic measurements will be provided by the wearable's IMUs. During sessions of motor-impairment assessments, we will capture more precise kinematics using a 10-camera motion capture system (VICON; 200 Hz). This system tracks the 3D positions of 40 markers placed on the legs and torso, and is equipped with suitable models for reconstructing bilateral angles of the hip, knee and ankle. | The assessment will be performed at 5.5 weeks | |
Secondary | Gait kinemetics | During FES sessions, kinematic measurements will be provided by the wearable's IMUs. During sessions of motor-impairment assessments, we will capture more precise kinematics using a 10-camera motion capture system (VICON; 200 Hz). This system tracks the 3D positions of 40 markers placed on the legs and torso, and is equipped with suitable models for reconstructing bilateral angles of the hip, knee and ankle. | The assessment will be performed at 2.5 weeks | |
Secondary | Gait kinemetics | During FES sessions, kinematic measurements will be provided by the wearable's IMUs. During sessions of motor-impairment assessments, we will capture more precise kinematics using a 10-camera motion capture system (VICON; 200 Hz). This system tracks the 3D positions of 40 markers placed on the legs and torso, and is equipped with suitable models for reconstructing bilateral angles of the hip, knee and ankle. | The assessment will be performed at 4 weeks | |
Secondary | Fugl-Meyer assessment score (lower-limb) | Lower-limb motor function assessment | The assessment will be performed at baseline | |
Secondary | Fugl-Meyer assessment score (lower-limb) | Lower-limb motor function assessment | The assessment will be performed at 5.5 weeks | |
Secondary | Fugl-Meyer assessment score (lower-limb) | Lower-limb motor function assessment | The assessment will be performed at 2.5 weeks | |
Secondary | Fugl-Meyer assessment score (lower-limb) | Lower-limb motor function assessment | The assessment will be performed at 4 weeks | |
Secondary | Mini-BEStest | Balance test | The assessment will be performed at baseline | |
Secondary | Mini-BEStest | Balance test | The assessment will be performed at 5.5 weeks | |
Secondary | Mini-BEStest | Balance test | The assessment will be performed at 2.5 weeks | |
Secondary | Mini-BEStest | Balance test | The assessment will be performed at 4 weeks |
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