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Effect of tACS on the Recovery of Motor Control of the Upper Limb and Cerebral Connectivity in Chronic Stroke Patients (tACS)

Primary Purpose

Chronic Stroke, Rehabilitation

Status
Recruiting
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
transcranial alternating current stimulation 70 Hz
Training
transcranial alternating current stimulation 7 Hz
transcranial alternating current stimulation Sham
Sponsored by
Universidad Metropolitana de Ciencias de la Educacion
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Stroke focused on measuring transcranial alternating current stimulation, motor recovery, stroke rehabilitation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of unilateral stroke at chronic stage (6 months or more) Upper Extremity -Fugl Meyer > 10 Wrist extensors strength of the paretic limb of 2 or more in the Medical Research Council (MRC) scale Active shoulder movement (flexion or abduction) of 30º or more Be able to follow the instructions necessary to achieve the training protocol Exclusion Criteria: Have a cerebellar stroke or ataxia Have some medical condition contraindicated for tACS (epilepsy, pacemaker, prosthesis between others) Have post-stroke epilepsy Limited passive range of motion in the elbow (less than 45º in flexo-extension plane) Limited passive range of motion in the wrist (less than 40º in flexo-extension plane) Limited passive range of motion in the shoulder (less than 70º in flexo-extension plane) Have another neurological condition that leads to upper extremity sequelae Have a normal performance in the clinical test

Sites / Locations

  • Centro de Habilidades Clínicas - Universidad Metropolitana de Ciencias de la EducaciónRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Sham Comparator

Arm Label

tACS - 70 Hz group

tACS - 7 Hz group

tACS - sham group

Arm Description

The group will receive the training program plus 20 minutes of tACS at 70 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) during a specific kinetic and kinematic tasks in every training session.

The group will receive the training program plus 20 minutes of tACS at 7 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) during a specific kinetic and kinematic tasks in every training session.

The group will receive the training program plus 30 seconds of tACS at 70 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) in every training session.

Outcomes

Primary Outcome Measures

Impairment Measure pre-intervention: Upper Extremity Fugl Meyer
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
Change of Impairment Measure post-intervention: Upper Extremity Fugl Meyer
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
Change of Impairment Measure follow up: Upper Extremity Fugl Meyer
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
EEG spectral power in Beta band pre-intervention
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks
Change in EEG spectral power in Beta band post-intervention
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks
Change in EEG spectral power in Beta band follow up
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks

Secondary Outcome Measures

Activity Measure: Action Research Arm Test
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Change in Activity Measure post-intervention: Action Research Arm Test
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Change in Activity Measure follow up: Action Research Arm Test
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Performance measure in the trained kinetic task (behavioral parameter)
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of how the participants performed the kinetic task
Change in the performance measure in the trained kinetic task post-intertenvion (behavioral parameter)
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinetic task at the beginning of the training protocol and at the end.
Change in the performance measure in the trained kinetic task at follow up (behavioral parameter)
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinetic task at the beginning of the training protocol and at the 12 week follow up.
Performance measure in trained kinematic task (behavioral parameter)
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of how the participants performed the kinematic task
Change in the performance measure in the trained kinematic task post-intervention (behavioral parameter)
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measure the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinematic task at the beginning of the training protocol and at the end.
Change in performance measure in the trained kinematic task at follow up (behavioral parameter)
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measure the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinematic task at the beginning of the training protocol and at the end.

Full Information

First Posted
June 12, 2023
Last Updated
July 12, 2023
Sponsor
Universidad Metropolitana de Ciencias de la Educacion
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1. Study Identification

Unique Protocol Identification Number
NCT05947318
Brief Title
Effect of tACS on the Recovery of Motor Control of the Upper Limb and Cerebral Connectivity in Chronic Stroke Patients
Acronym
tACS
Official Title
Effect of Transcranial Alternating Current Stimulation on the Recovery of Motor Control of the Upper Limb and Cerebral Connectivity in Chronic-stage Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 2, 2023 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Metropolitana de Ciencias de la Educacion

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project seeks to evaluate the effect of transcranial alternating current stimulation (tACS) on the recovery of motor control of the upper limb and associated neuronal synchrony during a 14-sessions (5-week) rehabilitation program for adult patients with diagnosis of stroke at chronic stage. Specifically, the stimulation on Gamma ranges, because the evidence available so far allows us to propose that the tACS in the Gamma range (around 70 Hz) facilitates motor execution. For this purpose, the experimental approach involves active (70 Hz in Gamma rhythm and 7 Hz, Theta rhythm) and sham tACS together with an analytical and integrated motor training with a double-blind and randomized design. Our hypothesis is that Gamma frequency tACS restores neuronal synchrony in Beta range, which enhances the upper limb motor recovery associated with a training program. Using specific motor control parameters, clinical scales and electroencephalography, the immediate and long-term (3 months after finished the training) behavioral and neurophysiological effect of this new neurostimulation paradigm (tACS plus training) for motor rehabilitation of stroke will be established.
Detailed Description
This project seeks to evaluate the effect of transcranial alternating current stimulation (tACS) on the recovery of motor control of the upper limb and associated neuronal synchrony during a 14 sessions (5 week) rehabilitation program for adult patients with diagnosis of stroke at chronic stage. Specifically, the stimulation on Gamma ranges, because the evidence available so far allows us to propose that the tACS in the Gamma range (around 70 Hz) facilitates motor execution. For this purpose, the experimental approach involves active (70 Hz in Gamma rhythm and 7 Hz, Theta rhythm) and sham tACS together with an analytical and integrated motor training with a double-blind and randomized design. Our hypothesis is that Gamma frequency tACS restores neuronal synchrony in Beta range, which enhances the upper limb motor recovery associated with a training program. The general objective is to assess the effects of a combined program of tACS and upper limb training on motor performance and brain connectivity in chronic-stage stroke patients. The specifics objectives to accomplish this are (1) Implement a system for simultaneous measurement of motor activity and EEG under tACS, considering possible postural alterations in stroke patients. (2) Evaluate the upper limb motor control and neuronal synchrony associated with motor performance during the execution of a combined stimulation and training program. Training will include analytical and functional tasks to optimize the performance in function and activity ICF level. tACS will be applied only during analytical task. (3) Analyze the changes in motor performance and neuronal synchrony for the experimental groups. Using specific motor control parameters (kinetic and kinematic control), clinical scales and electroencephalography, the immediate and long-term (3 months after finished the training) behavioral and neurophysiological effect of this new neurostimulation paradigm (tACS plus training) for motor rehabilitation of stroke will be established. By means of analysis of variance, clustering comparisons and linear regressions, it will be established the effect of tACS on neuronal synchrony and the parallel motor activity, as well as their underlying relationship. We will use the REDCap platform to register all the clinical data given by the medical record and clinical assessments. The recruitment will be made at the Clinical Center of Metropolitan University of Educational Sciences and in the Primary Care Centers that are near to the University. The sample size is 45 chronic stage stroke survivors. The sample size calculation used the data available in the study for the difference in Fugl-Meyer score between the bihemispheric and sham transcranial Direct Current Stimulation groups after the intervention (in the study of Alisar et al, 2020), considering an effect size of 1.4, a p-value of 0.05 and a power (1- beta) of 0.9, which yielded a sample size of 12 subjects per group. Now, also considering an attrition percentage of 20% and an equivalence in the size of the 3 study groups, the final sample size is 15 people per group (45 people in total). To answer the study hypothesis, two variables will be examined as primary results: Behavioral level, it will be the score on the Fugl-Meyer scale (upper extremity section). This scale has been widely used in the field of neurorehabilitation to assess motor impairments (ICF function level). Neurophysiological level, the primary outcome will be the change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks. Signal processing will follow a cluster approach using the Fieldtrip toolbox in Matlab software (R2016B). Both variables will be subjected to a two-factor analysis of variance (experimental group factor (3 levels, tACS-70Hz, 7Hz and simulated) and time factor (4 levels referred to the measurement times)). Depending on the result, it will apply a post-hoc test (bonferroni) to study differences between levels and interactions. The association between the variables will be inspected through regression models. The level of significance will have a p-value of 0.05. The statistical analysis will be implemented in the R language and the Rstudio software. Complementary to the primary results, and in order to broaden the description of the study phenomenon, the scores of the clinical scales already described will be analyzed, as well as kinetic (absolute force, speed of force change) and kinematic variables (direction error, maximum speed) of the analytical and combined tasks. In addition, the long-scale synchrony will be described by means of connectivity variables between the electrodes already identified (phase locking value and weighted phase lag index).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Stroke, Rehabilitation
Keywords
transcranial alternating current stimulation, motor recovery, stroke rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Three experimental groups: tACS-70 Hz group tACS-7Hz group tACS-sham group
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Neither the participant or the professionals that will make the training and the assessments will know to which group the participants was assigned.
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
tACS - 70 Hz group
Arm Type
Experimental
Arm Description
The group will receive the training program plus 20 minutes of tACS at 70 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) during a specific kinetic and kinematic tasks in every training session.
Arm Title
tACS - 7 Hz group
Arm Type
Active Comparator
Arm Description
The group will receive the training program plus 20 minutes of tACS at 7 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) during a specific kinetic and kinematic tasks in every training session.
Arm Title
tACS - sham group
Arm Type
Sham Comparator
Arm Description
The group will receive the training program plus 30 seconds of tACS at 70 Hz in the C3 or C4 electrode position (depending of the hemiparetic arm) in every training session.
Intervention Type
Device
Intervention Name(s)
transcranial alternating current stimulation 70 Hz
Intervention Description
Transcranial alternating current stimulation in the head above the motor cortex area of one side of the brain, according to the hemiparesis side. Electrodes with 3.14 cm2 of stimulation area will be used, therefore, the initial current intensity will be 0.21 mA, with a current density of 0.07 mA / cm2. The current intensity will be adjusted to the tactile sensory threshold and phosphenes of each patient, with in order to reduce such sensory effects, but considering that the decrease in current will not be greater than 10% of the initial intensity, in order to obtain a comparable configuration between subjects. The frequency stimulation will be 70 Hz
Intervention Type
Behavioral
Intervention Name(s)
Training
Intervention Description
Training of the upper limb with specific kinematic and kinetic tasks plus functional training
Intervention Type
Device
Intervention Name(s)
transcranial alternating current stimulation 7 Hz
Intervention Description
Transcranial alternating current stimulation in the head above the motor cortex area of one side of the brain, according to the hemiparesis side. Electrodes with 3.14 cm2 of stimulation area will be used, therefore, the initial current intensity will be 0.21 mA, with a current density of 0.07 mA / cm2. The current intensity will be adjusted to the tactile sensory threshold and phosphenes of each patient, with in order to reduce such sensory effects, but considering that the decrease in current will not be greater than 10% of the initial intensity, in order to obtain a comparable configuration between subjects. The frequency stimulation will be 7 Hz
Intervention Type
Device
Intervention Name(s)
transcranial alternating current stimulation Sham
Intervention Description
Transcranial alternating current stimulation in the head above the motor cortex area of one side of the brain, according to the hemiparesis side. Electrodes with 3.14 cm2 of stimulation area will be used, therefore, the initial current intensity will be 0.21 mA, with a current density of 0.07 mA / cm2. The current intensity will be adjusted to the tactile sensory threshold and phosphenes of each patient, with in order to reduce such sensory effects, but considering that the decrease in current will not be greater than 10% of the initial intensity, in order to obtain a comparable configuration between subjects. The stimulation will be turn on for 30 seconds (at 70 Hz)
Primary Outcome Measure Information:
Title
Impairment Measure pre-intervention: Upper Extremity Fugl Meyer
Description
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
Time Frame
week 0
Title
Change of Impairment Measure post-intervention: Upper Extremity Fugl Meyer
Description
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
Time Frame
week 5 or 6 (end of the training program)
Title
Change of Impairment Measure follow up: Upper Extremity Fugl Meyer
Description
Scale use to assess motor impairments (ICF function level), and adequately reflects the analytical motor control of force and direction of movement. The scale has a maximum of 66 points, which indicates a normal performance. Lower scores indicate worse performance.
Time Frame
week 12
Title
EEG spectral power in Beta band pre-intervention
Description
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks
Time Frame
week 0
Title
Change in EEG spectral power in Beta band post-intervention
Description
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks
Time Frame
week 5 or 6 (end of the training program)
Title
Change in EEG spectral power in Beta band follow up
Description
Change in spectral power in the Beta band (13-30Hz) associated with motor performance in kinetic and kinematic tasks
Time Frame
week 12
Secondary Outcome Measure Information:
Title
Activity Measure: Action Research Arm Test
Description
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Time Frame
week 0, week 5 or 6 (end of the training program) and week 12
Title
Change in Activity Measure post-intervention: Action Research Arm Test
Description
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Time Frame
week 5 or 6 (end of the training program)
Title
Change in Activity Measure follow up: Action Research Arm Test
Description
Action Research Arm Test will be used to evaluate de ICF activity level. The maximum score is 57, which indicate a normal perfomance. Lower scores indicate worse performance.
Time Frame
week 12
Title
Performance measure in the trained kinetic task (behavioral parameter)
Description
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of how the participants performed the kinetic task
Time Frame
week 0, week 5 or 6 (end of the training program) and week 12
Title
Change in the performance measure in the trained kinetic task post-intertenvion (behavioral parameter)
Description
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinetic task at the beginning of the training protocol and at the end.
Time Frame
week 5 or 6 (end of the training program)
Title
Change in the performance measure in the trained kinetic task at follow up (behavioral parameter)
Description
The change that we observed in the kinetic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinetic task at the beginning of the training protocol and at the 12 week follow up.
Time Frame
week 12
Title
Performance measure in trained kinematic task (behavioral parameter)
Description
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measures the change in the task that is trained in the training protocol. It is a measure of how the participants performed the kinematic task
Time Frame
week 0, week 5 or 6 (end of the training program) and week 12
Title
Change in the performance measure in the trained kinematic task post-intervention (behavioral parameter)
Description
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measure the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinematic task at the beginning of the training protocol and at the end.
Time Frame
week 5 or 6 (end of the training program)
Title
Change in performance measure in the trained kinematic task at follow up (behavioral parameter)
Description
The change that we observed in the kinematic task in the protocol training. This outcome is a behavioral parameter that measure the change in the task that is trained in the training protocol. It is a measure of the change in the performance in the kinematic task at the beginning of the training protocol and at the end.
Time Frame
week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of unilateral stroke at chronic stage (6 months or more) Upper Extremity -Fugl Meyer > 10 Wrist extensors strength of the paretic limb of 2 or more in the Medical Research Council (MRC) scale Active shoulder movement (flexion or abduction) of 30º or more Be able to follow the instructions necessary to achieve the training protocol Exclusion Criteria: Have a cerebellar stroke or ataxia Have some medical condition contraindicated for tACS (epilepsy, pacemaker, prosthesis between others) Have post-stroke epilepsy Limited passive range of motion in the elbow (less than 45º in flexo-extension plane) Limited passive range of motion in the wrist (less than 40º in flexo-extension plane) Limited passive range of motion in the shoulder (less than 70º in flexo-extension plane) Have another neurological condition that leads to upper extremity sequelae Have a normal performance in the clinical test
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juan J Mariman, Ph.D
Phone
+56981928168
Email
juan.mariman@umce.cl
First Name & Middle Initial & Last Name or Official Title & Degree
Trinidad B Bruna, MSc.
Phone
+34657278264
Email
trinidad.bruna@umce.cl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan J Mariman, Ph.D
Organizational Affiliation
Universidad Metropolitana de Ciencias de la Educacion
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro de Habilidades Clínicas - Universidad Metropolitana de Ciencias de la Educación
City
Santiago
ZIP/Postal Code
7780450
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juan J Mariman, PhD
Phone
+56081928168
Email
juan.mariman@umce.cl
First Name & Middle Initial & Last Name & Degree
Trinidad B Bruna, MSc
Phone
+34657278264
Email
trinidad.bruna@umce.cl

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
For now, we have no plans of sharing individual participant data.
Citations:
PubMed Identifier
31699572
Citation
Alisar DC, Ozen S, Sozay S. Effects of Bihemispheric Transcranial Direct Current Stimulation on Upper Extremity Function in Stroke Patients: A randomized Double-Blind Sham-Controlled Study. J Stroke Cerebrovasc Dis. 2020 Jan;29(1):104454. doi: 10.1016/j.jstrokecerebrovasdis.2019.104454. Epub 2019 Nov 4.
Results Reference
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Effect of tACS on the Recovery of Motor Control of the Upper Limb and Cerebral Connectivity in Chronic Stroke Patients

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