search
Back to results

Targeted Noninvasive Brain Stimulation (T-NIBS) to Improve Hand Motor Functions in Acquired Brain Injury

Primary Purpose

Upper Extremity Dysfunction, Traumatic Brain Injury

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Active High-definition Transcranial Direct Current Stimulation (HD-tDCS)
MusicGlove
Sponsored by
Kessler Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Upper Extremity Dysfunction focused on measuring HD-tDCS, TBI, Upper limb rehab, hand dexterity, MusicGlove, Noninvasive Brain Stimulation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:18 and 75 years

  • Confirmed diagnosis of Acquired brain injury (individuals with stroke or Traumatic Brain Injury)
  • At least 6 months post-injury
  • Complaints of weak movement of hands and fingers
  • Ability to understand the instructions that are part of the tDCS-MusicGlove testing and intervention
  • Willingness and ability to participate in and travel to Kessler Foundation for the baseline assessment visits, 10 training visits, and post-training follow-up visits
  • Ability to sit and be active for 2 hours on a chair (or wheelchair) without cardiac, respiratory and/or pain disturbances as assessed during the screening visit.
  • Willingness to give written informed consent.
  • Medically stable and not planning for a major change in medications for at least 4 months

Exclusion Criteria:

  • Unable to move the hand because of muscle stiffness (scoring 3 or more on the Ashworth scale)
  • Have lost the sensation of hand movement
  • Have a history of alcohol abuse and/or illicit drug use
  • Have a problem with the eyesight that would make it difficult to notice the changing instructions on a computer screen
  • Currently enrolled in another research study that might affect this research study
  • A history of epilepsy (including family members who are diagnosed with epilepsy)
  • An active history of migraine or chronic headache
  • A history of mental illness (e.g. schizophrenia, anxiety, depression, and PTSD)
  • Past or current history of treated ringing in the ears known as tinnitus or severe hearing problems
  • Have a tattoo with metal-based ink in the head or neck.
  • Have severe skin damage on the scalp
  • Afraid of confined spaces (claustrophobic)
  • Have metallic implants, including intracranial electrodes, surgical clips, shrapnel or a pacemaker.
  • Currently taking medications that increase the risk of seizures
  • Pregnant

Sites / Locations

  • Kessler FoundationRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

MusicGlove and Active HD-tDCS

MusicGlove and Sham HD-tDCS

Arm Description

During Active HD-tDCS, current up to 2mA will be delivered transiently for only 30 seconds and it will be turned ON for the remainder of 20 minutes.

During Sham HD-tDCS, current up to 2mA will be delivered transiently for only 30 seconds to simulate the real-tDCS based skin sensation.

Outcomes

Primary Outcome Measures

Change scores of Box and Block test (BBT)
BBT is an easy-to-evaluate inexpensive test which mainly evaluates the unilateral gross dexterity. The MusicGlove exercise that is proposed in this study recruits the finger muscles which are for fine motor coordination. During this test, the participant will be asked to move one-by-one, the maximum number of blocks from one compartment of a box to another of equal size, within 60 seconds.
Change scores of Upper-extremity Fugl-Myer Assessment (UEFMA)
Upper extremity Fugl-Meyer Assessment Score (UEFMA) primarily evaluates the functions of Shoulder/Elbow and Forearm, Wrist, Hand and Coordination and Speed in a series of performed tasks. The maximum score associated with the UE-FMA is 66 points. Each of the 33 specific tasks is scored as either 0 or an absence of function to a maximum score of 2 for the tasks being fully completed. The partial function can be scored as 1 for selected tasks. The change in scores from baseline-to-post-intervention and post-intervention-to-2-month-followup will be assessed.

Secondary Outcome Measures

Change scores of Action Research Arm Test (ARAT)
ARAT assesses the subject's ability to handle objects differing in size, weight and shape and therefore can be considered to be an arm-specific measure of activity limitation. ARAT is well-suited as a functional outcome measure in this study considering the type of hand exercise intervention.
Change scores of Nine Hole Peg Test (NHPT)
NHPT is a secondary outcome measure of finger dexterity that can be used in TBI with upper extremity motor deficits. It is considered to be a reliable measure of hand dexterity and recommended for inclusion in NIH toolbox Assessment of Neurological and Behavioral Function. NHPT requires participants to repeatedly place nine pegs into nine holes, one at a time, as quickly as possible and then remove them from the holes. The total time needed to complete the task is then recorded.
Change scores of Dexterity and Speed Test (DAST)
DAST is exclusively developed for MusicGlove performance assessment, and it was designed to evaluate how well subjects could respond to the sequence of music notes that continuously sped up. This measure is shown to be well correlated with the Box and Block test.
Changes in the Cortical Excitability using Motor Evoked Potentials (MEP)
MEP outcome measures have become the norm in brain stimulation studies. We hypothesize that the MEP amplitude and latency before- and after-intervention would reveal more information about the neuroplasticity changes during motor recovery. The motor evoked potential (MEP) will be provided by twenty unconditioned stimuli (120% RMT).
Quality of Life After Brain Injury (QOLIBRI)
Quality of Life After Brain Injury is a self-reported assessment that describes the health-related quality of life after Traumatic Brain Injury. QOLIBRI is specifically tailored for TBI-related dysfunctions.
Changes in the Functional Connectivity of the brain
Weighted Node degree (as an EEG functional connectivity measure) will reveal the overall importance of an area in the brain network. With the use of EEG-based graph-theoretic measure, we can assess the importance of which particular motor networks are involved in the motor recovery upon intervention.

Full Information

First Posted
July 29, 2019
Last Updated
June 8, 2023
Sponsor
Kessler Foundation
search

1. Study Identification

Unique Protocol Identification Number
NCT04057105
Brief Title
Targeted Noninvasive Brain Stimulation (T-NIBS) to Improve Hand Motor Functions in Acquired Brain Injury
Official Title
Targeted Noninvasive Brain Stimulation (T-NIBS) for Upper Extremity Motor Rehabilitation in Acquired Brain Injury (ABI) Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kessler Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Acquired Brain Injury (TBI) is a serious medical and health problem in the US. Individuals with an acquired brain injury due to stroke and Traumatic Brain Injury (TBI) commonly suffer from upper extremity physical impairments that persist even after years of injury; these deficits are attributed to the damage to brain structure and changes in structural and functional connectivity. Although the conventional rehabilitation approaches are helpful in assisting motor recovery often there is a complaint of fatigue due to the repetitive tasks and also, nearly half of the ABI survivors do not regain their ability to use their arms for daily activities. To address this issue, Dr. Shenoy's proposed study will investigate the combined use of individually targeted non-invasive brain stimulation and music-assisted video game-based hand exercises to achieve functional recovery. Further, the project will also investigate how the intervention modulates brain activity (recorded using EEG) in terms of brain connectivity before- and after the -intervention. In the end, this study will allow us to understand the cortical dynamics of ABI rehabilitation upon brain stimulation. Extending further, this could pave the way to advance the knowledge of behavioral and neural aspects of motor control in patients with different types of neuromuscular disorders.
Detailed Description
Persistent physical deficits associated with upper extremities including motor weakness, spasticity, and the lack of bimanual coordination of fingers, hands, and arms are particularly problematic as it results in serious disruption of many instrumental activities of daily living. Conventional physical and occupational therapy help improve motor recovery in ABI but nearly 50% of the patients still suffer from a significant level of upper limb motor impairment following rehabilitation, undermining the need for novel therapeutic approaches to improve recovery. Non-invasive brain stimulation (NIBS) techniques such as Transcranial Direct Current Stimulation (tDCS) have shown great promises as adjuvant means to improve the efficacy of neurorehabilitation in Stroke. However, the benefit of combining NIBS with regular motor training has not been extensively studied in the TBI population. One of the inherent challenges with the approach in dealing with the heterogeneity of the TBI population in terms of the type of injury and the location of the affected cortical region which warrants personalized intervention than a one-size-fits-all approach. Therefore, we propose to develop an individually targeted high-definition tDCS (HD-tDCS) protocol to optimize its effect and achieve maximal upper limb motor recovery in each patient by stimulating the hand knob region which is close to precentral gyrus. HD-tDCS will be combined with MusicGlove exercises (music-assisted repetitive finger movements) to improve the neuroplasticity (adaptation and reorganization to compensate for the initial insult and to attempt to restore function) and fine motor learning while keeping patients engaged. Using a double-blind design, 24 individuals with an acquired brain injury will be randomized to either receive real or sham HD-tDCS during MusicGlove therapy to assess the added benefit of HD-tDCS. In addition, we aim to investigate the underlying neural mechanism of HD-tDCS on motor recovery by studying change in EEG based brain connectivity because of the intervention. The short-term significance of this project will be to validate the effectiveness of HD-tDCS in ABI neurorehabilitation and help better understand the underlying cortical mechanism of the improvement. In the long-term, the findings of this pilot study will contribute toward the development of an optimal patient-specific rehabilitation therapy to maximize motor recovery in individuals with neuromuscular disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Upper Extremity Dysfunction, Traumatic Brain Injury
Keywords
HD-tDCS, TBI, Upper limb rehab, hand dexterity, MusicGlove, Noninvasive Brain Stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
double-blinded (participant and the investigator are blinded from knowing the HD-tDCS allocation sequence)
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MusicGlove and Active HD-tDCS
Arm Type
Active Comparator
Arm Description
During Active HD-tDCS, current up to 2mA will be delivered transiently for only 30 seconds and it will be turned ON for the remainder of 20 minutes.
Arm Title
MusicGlove and Sham HD-tDCS
Arm Type
Sham Comparator
Arm Description
During Sham HD-tDCS, current up to 2mA will be delivered transiently for only 30 seconds to simulate the real-tDCS based skin sensation.
Intervention Type
Device
Intervention Name(s)
Active High-definition Transcranial Direct Current Stimulation (HD-tDCS)
Intervention Description
Stimulation sessions will be conducted once a day on 10 weekdays over a period of 2-3 weeks. Anodal HD-tDCS will be delivered either in Active or Sham mode (as per the randomized order) in a 4x1 ring configuration (center electrode being Anode and the surrounding 4 electrodes being cathodes) over the affected motor area.
Intervention Type
Device
Intervention Name(s)
MusicGlove
Intervention Description
Both groups will undergo MusicGlove video-game based hand exercises.
Primary Outcome Measure Information:
Title
Change scores of Box and Block test (BBT)
Description
BBT is an easy-to-evaluate inexpensive test which mainly evaluates the unilateral gross dexterity. The MusicGlove exercise that is proposed in this study recruits the finger muscles which are for fine motor coordination. During this test, the participant will be asked to move one-by-one, the maximum number of blocks from one compartment of a box to another of equal size, within 60 seconds.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Change scores of Upper-extremity Fugl-Myer Assessment (UEFMA)
Description
Upper extremity Fugl-Meyer Assessment Score (UEFMA) primarily evaluates the functions of Shoulder/Elbow and Forearm, Wrist, Hand and Coordination and Speed in a series of performed tasks. The maximum score associated with the UE-FMA is 66 points. Each of the 33 specific tasks is scored as either 0 or an absence of function to a maximum score of 2 for the tasks being fully completed. The partial function can be scored as 1 for selected tasks. The change in scores from baseline-to-post-intervention and post-intervention-to-2-month-followup will be assessed.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Secondary Outcome Measure Information:
Title
Change scores of Action Research Arm Test (ARAT)
Description
ARAT assesses the subject's ability to handle objects differing in size, weight and shape and therefore can be considered to be an arm-specific measure of activity limitation. ARAT is well-suited as a functional outcome measure in this study considering the type of hand exercise intervention.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Change scores of Nine Hole Peg Test (NHPT)
Description
NHPT is a secondary outcome measure of finger dexterity that can be used in TBI with upper extremity motor deficits. It is considered to be a reliable measure of hand dexterity and recommended for inclusion in NIH toolbox Assessment of Neurological and Behavioral Function. NHPT requires participants to repeatedly place nine pegs into nine holes, one at a time, as quickly as possible and then remove them from the holes. The total time needed to complete the task is then recorded.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Change scores of Dexterity and Speed Test (DAST)
Description
DAST is exclusively developed for MusicGlove performance assessment, and it was designed to evaluate how well subjects could respond to the sequence of music notes that continuously sped up. This measure is shown to be well correlated with the Box and Block test.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Changes in the Cortical Excitability using Motor Evoked Potentials (MEP)
Description
MEP outcome measures have become the norm in brain stimulation studies. We hypothesize that the MEP amplitude and latency before- and after-intervention would reveal more information about the neuroplasticity changes during motor recovery. The motor evoked potential (MEP) will be provided by twenty unconditioned stimuli (120% RMT).
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Quality of Life After Brain Injury (QOLIBRI)
Description
Quality of Life After Brain Injury is a self-reported assessment that describes the health-related quality of life after Traumatic Brain Injury. QOLIBRI is specifically tailored for TBI-related dysfunctions.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)
Title
Changes in the Functional Connectivity of the brain
Description
Weighted Node degree (as an EEG functional connectivity measure) will reveal the overall importance of an area in the brain network. With the use of EEG-based graph-theoretic measure, we can assess the importance of which particular motor networks are involved in the motor recovery upon intervention.
Time Frame
baseline (before intervention), Post-training (immediately after the end of 2-week intervention), Followup (2 months after the end of intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:18 and 75 years Confirmed diagnosis of Acquired brain injury (individuals with stroke or Traumatic Brain Injury) At least 6 months post-injury Complaints of weak movement of hands and fingers Ability to understand the instructions that are part of the tDCS-MusicGlove testing and intervention Willingness and ability to participate in and travel to Kessler Foundation for the baseline assessment visits, 10 training visits, and post-training follow-up visits Ability to sit and be active for 2 hours on a chair (or wheelchair) without cardiac, respiratory and/or pain disturbances as assessed during the screening visit. Willingness to give written informed consent. Medically stable and not planning for a major change in medications for at least 4 months Exclusion Criteria: Unable to move the hand because of muscle stiffness (scoring 3 or more on the Ashworth scale) Have lost the sensation of hand movement Have a history of alcohol abuse and/or illicit drug use Have a problem with the eyesight that would make it difficult to notice the changing instructions on a computer screen Currently enrolled in another research study that might affect this research study A history of epilepsy (including family members who are diagnosed with epilepsy) An active history of migraine or chronic headache A history of mental illness (e.g. schizophrenia, anxiety, depression, and PTSD) Past or current history of treated ringing in the ears known as tinnitus or severe hearing problems Have a tattoo with metal-based ink in the head or neck. Have severe skin damage on the scalp Afraid of confined spaces (claustrophobic) Have metallic implants, including intracranial electrodes, surgical clips, shrapnel or a pacemaker. Currently taking medications that increase the risk of seizures Pregnant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vikram Shenoy Handiru, PhD
Phone
9733243578
Email
vshenoy@kesslerfoundation.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guang Yue, PhD
Organizational Affiliation
Kessler Foundation
Official's Role
Study Director
Facility Information:
Facility Name
Kessler Foundation
City
West Orange
State/Province
New Jersey
ZIP/Postal Code
07052
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Venturini
Phone
973-324-3571
Email
jventurini@kesslerfoundation.org
First Name & Middle Initial & Last Name & Degree
Soha Saleh, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28579362
Citation
Beaulieu LD, Milot MH. Changes in transcranial magnetic stimulation outcome measures in response to upper-limb physical training in stroke: A systematic review of randomized controlled trials. Ann Phys Rehabil Med. 2018 Jul;61(4):224-234. doi: 10.1016/j.rehab.2017.04.003. Epub 2017 Jun 7.
Results Reference
background
PubMed Identifier
25180301
Citation
De Vico Fallani F, Richiardi J, Chavez M, Achard S. Graph analysis of functional brain networks: practical issues in translational neuroscience. Philos Trans R Soc Lond B Biol Sci. 2014 Oct 5;369(1653):20130521. doi: 10.1098/rstb.2013.0521.
Results Reference
background
PubMed Identifier
24885076
Citation
Friedman N, Chan V, Reinkensmeyer AN, Beroukhim A, Zambrano GJ, Bachman M, Reinkensmeyer DJ. Retraining and assessing hand movement after stroke using the MusicGlove: comparison with conventional hand therapy and isometric grip training. J Neuroeng Rehabil. 2014 Apr 30;11:76. doi: 10.1186/1743-0003-11-76.
Results Reference
background

Learn more about this trial

Targeted Noninvasive Brain Stimulation (T-NIBS) to Improve Hand Motor Functions in Acquired Brain Injury

We'll reach out to this number within 24 hrs