Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05760846
Other study ID # Bim-MSkL acute
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 17, 2023
Est. completion date October 2028

Study information

Verified date May 2023
Source University Hospital of Mont-Godinne
Contact Yves Vandermeeren, MD, PhD
Phone +32 81 42 33 21
Email yves.vandermeeren@uclouvain.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The subacute phase of stroke provides a window into how a lesion perturbs sensorimotor functions prior to reorganisation driven by plasticity and neurorehabilitation. The recovery from motor impairment has been extensively studied, but it is currently unknown whether motor skill learning (MSkL) is enhanced or impaired during acute stroke, especially bimanual motor skill learning (bim-MSkL), which likely requires more motor-attentional-cognitive resources than unimanual MSkL. The goals of this project are: to determine the neural substrates critical to achieve proximal and distal bimanual motor skill learning (bim-MSkL) by specifying whether (sub)acute stroke to different brain areas (cortical and subcortical) induce specific deficits in bimanual and/or distal bim-MSkL, which behavioral components are involved in bim-MSkL, and whether damage to the motor, sensory and inter-hemispheric pathways specifically impairs proximal and/or distal bim-MSkL.


Description:

Over 3 consecutive days, the patients will be evaluated and will train on the rehabilitation robot REAplan® (http://www.axinesis.com/) to assess proximal bim-MSkL and on the manual dexterity tool Dextrain Manipulandum (https://www.dextrain.com/) to assess distal bim-MSkL. For proximal bim-MSkL, patients will train over the 3 days on the serious game Circuit on the bimanual REAplan® and will be randomised to two different bimanual versions. By this means, the investigators will explore the components of bim-MSkL in acute stroke patients. The motor skill learning setup (Circuit) that was developed and successfully used in healthy individuals and stroke patients has already been implemented in the REAplan® environment and will be used as innovative serious games based on a speed/accuracy trade-off (SAT), allowing a detailed analysis of motor skill learning components (speed, accuracy, SAT, movement smoothness, dynamics...). For the serious game Circuit, who based on motor skill learning, the subjects will have to practice a complex circuit and move a cursor as quickly and accurately as possible by controlling the handles of the robot with both arms. For distal bim-MSkL, patients will train on a complex sequence of finger movements involving both hands. Each day, several successive repetitions of the sequence will be displayed, corresponding to one block. 3 to 6 blocks will be repeated, each separated by 30 sec of rest. After training on the third day, a new sequence will be repeated for 3 blocks to assess generalization. To explore the role of different brain structures in bim-MskL, Voxel-based Lesion Symptom Mapping (VLSM) based on high-resolution brain magnetic resonance imaging (MRI) scans, will be used to analyse the relationship between tissue damage and proximal/distal bim-MskL scores on a voxel-by-voxel basis. Diffusion Tensor Imaging (DTI) will quantify the integrity of several white matter tracts, allowing through correlation analyses to unveil the white matter tracts crucial to achieve proximal and/or distal bim-MskL. In addition, several "classical" clinical scales and tests will be used to evaluate overall motor-sensory-cognitive functions. In addition to the (sub)acute stroke patients, a group of healthy individuals who will not undergo MRI (n=60) will be enrolled as control group. Subjects in this group will also be randomized 1/1 in the two versions of the bimanual Circuit task on the REAplan® robot.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date October 2028
Est. primary completion date March 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility ACUTE STROKE PATIENTS: Inclusion Criteria: - acute stroke (< 21 days) - aged 18-90 years - with a demonstrated stroke (ischemic or hemorrhagic) lesion on brain imaging Exclusion Criteria: - " classical " contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...) - difficulty in understanding or executing commands - drug/alcohol abuse - severe aphasia / cognitive deficits interfering with study - inability to complete the tasks (i.e. full paralysis of the arm) - multiple strokes / dementia / psychiatric condition HEALTHY INDIVIDUALS: Inclusion Criteria: • 18-90 years Exclusion Criteria: - medical history with a previous stroke / relevant neurological deficit - drug/alcohol abuse - psychiatric condition/ dementia

Study Design


Related Conditions & MeSH terms


Intervention

Device:
REAplan®
motor skill learning with the REAplan® rehabilitation robot, to be performed with both arms
Dextrain Manipulandum®
motor skill learning with the Dextrain Manipulandum® dexterity tool to be performed with both hands

Locations

Country Name City State
Belgium CHU UCL Namur Yvoir Namur
Belgium University Hospital CHU Dinant Godinne UCL Yvoir

Sponsors (1)

Lead Sponsor Collaborator
University Hospital of Mont-Godinne

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary bimanual Speed/Accuracy Trade-off (bi-SAT), bimanual Speed/Accuracy Trade-off measured by the REAplan® robot bimanual Speed/Accuracy Trade-off: mathematical computation of the relationship between speed and accuracy change between baseline (Day 1) and after training (Day 3)
Primary bimanual Coordination factor (bi-CO), bimanual Coordination factor measured by the REAplan® robot bimanual Coordination factor, mathematical measure of the phase coherence between speeds of both arms change between baseline (Day 1) and after training (Day 3)
Primary bi-Force, bimanual force measured by the REAplan® robot bimanual forces, forces exerted in the wrong direction by each arm (Newtons) change between baseline (Day 1) and after training (Day 3)
Primary Root Mean Square Error (RMSE), bimanual root mean square error measured by the Dextrain Manipulandum Tracking error between the actual applied force and the target force change between baseline (Day 1) and after training (Day 3)
Primary Bimanual Dexterity Coordination Index measured by the Dextrain Manipulandum bimanual Coordination factor, mathematical measure of the phase coherence between speeds of both thumb-index clamps change between baseline (Day 1) and after training (Day 3)
Secondary Reaction time measured by the Dextrain Manipulandum time between the target appearance and when the force applied exceeds threshold change between baseline (Day 1) and after training (Day 3)
Secondary Rise time measured by the Dextrain Manipulandum time between the reaction time and reaching the plateau change between baseline (Day 1) and after training (Day 3)
Secondary Coactivation measured by the Dextrain Manipulandum binary measure of unasked fingers activated above the force threshold change between baseline (Day 1) and after training (Day 3)
Secondary Hold time measured by the Dextrain Manipulandum time of plateau maintenance change between baseline (Day 1) and after training (Day 3)
Secondary Voxel-based Lesion Symptom Mapping (VLSM) Diffusion Weighted Imaging (DWI) Baseline
Secondary Diffusion Tensor Imaging (DTI) Fractional Anisotropy Baseline
Secondary Fugl Meyer Upper Extremity Test (FMA-UE) Tests impairments of the upper limb after stroke. Range: 0-66. A higher score means less impairment. Day1
Secondary Arm Motor Ability (AMA) test Measure disabilities of the upper limb after stroke. Range: 0-100. A higher score means less disabilities in activities of daily living. Day 1
Secondary Montreal Cognitive Assessment (MoCA) Tests the short-term memory, visuospatial skills, executive functions, attention, concentration, working memory, language and orientation in time and space. Range: 0-30, higher score means no cognitive impairment. Day 1
Secondary Fatigue Visual Analog Scale (VAS) Visual Analog Scale to evaluate fatigue = a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points. Range : 0- 10. A higher score means a higher level of fatigue. Day 1
Secondary Shoulder Abduction Finger Extension (SAFE) test A prognostic determinant of the function of the hemiparetic upper limb (UL) after a stroke. For each of the 2 subitems, the range is 0-5. A score of 5 means normal power. A score of 0 means no contraction possible. Day 1
Secondary Modified Ashworth Scale (mAS) clinical measure of spasticity. For each of the 8 subitems, the range is 0-4. A higher score means a higher level of spasticity Day 1
See also
  Status Clinical Trial Phase
Recruiting NCT05378035 - DOAC in Chinese Patients With Atrial Fibrillation
Completed NCT03574038 - Transcranial Direct Current Stimulation as a Neuroprotection in Acute Stroke N/A
Completed NCT03679637 - Tablet-based Aphasia Therapy in the Acute Phase After Stroke N/A
Completed NCT03633422 - Evaluation of Stroke Patient Screening
Completed NCT04088578 - VNS-supplemented Motor Retraining After Stroke N/A
Not yet recruiting NCT05534360 - Tenecteplase Treatment in Ischemic Stroke Registry
Withdrawn NCT04991038 - Clinical Investigation to Compare Safety and Efficacy of DAISE and Stent Retrievers for Thrombectomy In Acute Ischemic Stroke Patients N/A
Not yet recruiting NCT04105322 - Effects of Kinesio Taping on Balance and Functional Performance in Stroke Patients N/A
Withdrawn NCT05786170 - ERILs Und SNILs Unter SOC N/A
Recruiting NCT03132558 - Contrast Induced Acute Kidney in Patients With Acute Stroke N/A
Completed NCT02893631 - Assessment of Hemostasis Disorders in rtPA-treated Patients Requiring Endovascular Treatment for Ischemic Stroke
Active, not recruiting NCT02274727 - Biomarker Signature of Stroke Aetiology Study: The BIOSIGNAL-Study
Completed NCT02225730 - Imaging Collaterals in Acute Stroke (iCAS)
Terminated NCT01705353 - The Role of HMGB-1 in Chronic Stroke N/A
Active, not recruiting NCT01581502 - SAMURAI-NVAF Study: Anticoagulant Therapy for Japanese Stroke Patients With Nonvalvular Atrial Fibrillation (NVAF) N/A
Completed NCT01182818 - Fabry and Stroke Epidemiological Protocol (FASEP): Risk Factors In Ischemic Stroke Patients With Fabry Disease N/A
Completed NCT00761982 - Autologous Bone Marrow Stem Cells in Middle Cerebral Artery Acute Stroke Treatment. Phase 1/Phase 2
Completed NCT00535197 - Autologous Bone Marrow Stem Cells in Ischemic Stroke. Phase 1/Phase 2
Terminated NCT00132509 - FRALYSE Trial: Comparison of the Classical Rt-PA Procedure With a Longer Procedure in Acute Ischemic Stroke Phase 2
Recruiting NCT05760326 - Diagnostic and Prognostic Role of Clot Analysis in Stroke Patients