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A Study of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for Stroke (nBETTER)

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
nBETTER
Sponsored by
Tan Tock Seng Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Stroke

Eligibility Criteria

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

Inclusion Criteria:

  1. Aged 21-80 years with first-ever clinical stroke diagnosed on CT or MRI brain imaging.
  2. Stroke duration of 3-24 months.
  3. Stroke type: ischemic or haemorrhagic
  4. Fugl-Meyer motor score of the upper limb range from 10-50
  5. Ability to pay attention and maintain supported sitting for 1.5 hours continuously
  6. Able to give own consent and understand simple instructions
  7. Fulfils BCI resting brain states on initial screening.

Exclusion Criteria:

  1. Recurrent clinical stroke
  2. Functional status: severe aphasia or inattention, unstable medical conditions which may affect participation (e.g. unresolved sepsis, postural hypotension, end stage renal failure) or anticipated life expectancy of <1 year due to malignancy or neurodegenerative disorder)
  3. Hemispatial neglect (visual or sensory) or severe visual impairment despite visual aids
  4. History of epilepsy, severe depression or active psychiatric disorder
  5. Skull defect or previous cranial surgery as this would affect physical fit of EEG cap interface
  6. Local arm factors: severe spasticity Modified Ashworth scale >2 in any region, visual analogue scale (VAS score) >4/10, fixed joint contractures or joint replacements, patients with poor skin conditions which would contraindicate repetitive arm training.
  7. TMS contraindications: females with reproductive potential not on reliable contraception; pregnancy; cardiac pacemakers; orthodontics (braces); metal implants.

Sites / Locations

  • Tan Tock Seng Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

nBETTER and Conventional Therapy

Arm Description

Intervention: nBetter therapy

Outcomes

Primary Outcome Measures

Change in Upper extremity Fugl-Meyer motor score post training
As above

Secondary Outcome Measures

Change in Transcranial Magnetic Stimulation Assessment (TMS)
As above
Change in Grip Strength
Grip Strength measures hand force in kgf
Change in Frenchay Arm Test of Function (FAT)
Frenchay Arm Test of Function (FAT) measures 5 tasks: Stabilize ruler and draw line Grasp and lift cylinder without dropping Pick up half glass and drink Replace sprung clothes peg Comb hair from top down (sides and back of head)
Change in Modified Ashworth Scale score (MAS)
Modified Ashworth Scale score (MAS) measure spasticity of wrist and hand finger flexors on a scale from 0 to 4
Change in Visual Analogue Scale (VAS)
Visual Analogue Scale (VAS) measures pain on a scale from 0 to 10

Full Information

First Posted
April 7, 2016
Last Updated
February 25, 2018
Sponsor
Tan Tock Seng Hospital
Collaborators
Institute for Infocomm Research, National University Hospital, Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT02765334
Brief Title
A Study of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for Stroke
Acronym
nBETTER
Official Title
A Pilot Feasibility Clinical Trial of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for postStroke Arm Paresis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
December 28, 2015 (Actual)
Primary Completion Date
August 16, 2017 (Actual)
Study Completion Date
August 16, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tan Tock Seng Hospital
Collaborators
Institute for Infocomm Research, National University Hospital, Singapore

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A feasibility trial of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) system for Brain Computer Interface (BCI) neurofeedback for rehabilitation of the subacute and chronic hemiplegic upper limb aimed at improving upper limb recovery for subacute to chronic stroke patients.
Detailed Description
Stroke remains the 4th cause of death in Singapore and despite advances in neuro-medical care and rehabilitation, 40-50% of stroke survivors are left with permanent neuro-disability and a reduced quality of life. The previous 2 decades has seen exponential leaps in the development of rehabilitation technologies which enhance neuroplasticity and rehabilitation outcome. One of these potentially useful technologies is nBETTER System, was developed by Institute for Infocomm Research, Agency for Science, Technology and Research (A*STAR). nBETTER is a portable, internet-connected device that detects the imagination of movement of stroke-affected limb using a Electroencephalography (EEG)-based Brain-Computer Interface (BCI) thus delivering visually engaging feedback for directed neurofeedback aimed at improving upper limb recovery for subacute to chronic stroke patients. The pilot study aims to recruit 13 patients using a multi centre trial design to investigate nBETTER system feasibility and safety for rehabilitation of subacute to chronic stroke patients with upper limb motor impairment and to determine clinical efficacy, safety and feasibility of such a system when it is delivered with standard occupational therapy. The investigators primary hypothesis is that nBETTER is a feasible and safe prototype in stroke survivors (> 3 months) with moderate to severe arm impairment (FMMA 10-50). The primary outcome is a gain of 15% in Fugl-Meyer motor scores at 6 weeks after 18 sessions (total of 27 hours) of supervised training by occupational therapists and bioengineers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Feasibility of nBETTER training (60 minutes) with conventional arm therapy (30minutes) for chronic stroke.
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
nBETTER and Conventional Therapy
Arm Type
Experimental
Arm Description
Intervention: nBetter therapy
Intervention Type
Device
Intervention Name(s)
nBETTER
Intervention Description
60 minutes of nBETTER training followed by 30 minutes of conventional therapy occupational therapy. Total of 18 sessions over 6 weeks.
Primary Outcome Measure Information:
Title
Change in Upper extremity Fugl-Meyer motor score post training
Description
As above
Time Frame
Baseline and week 6
Secondary Outcome Measure Information:
Title
Change in Transcranial Magnetic Stimulation Assessment (TMS)
Description
As above
Time Frame
Baseline and week 6
Title
Change in Grip Strength
Description
Grip Strength measures hand force in kgf
Time Frame
Baseline and week 6
Title
Change in Frenchay Arm Test of Function (FAT)
Description
Frenchay Arm Test of Function (FAT) measures 5 tasks: Stabilize ruler and draw line Grasp and lift cylinder without dropping Pick up half glass and drink Replace sprung clothes peg Comb hair from top down (sides and back of head)
Time Frame
Baseline and week 6
Title
Change in Modified Ashworth Scale score (MAS)
Description
Modified Ashworth Scale score (MAS) measure spasticity of wrist and hand finger flexors on a scale from 0 to 4
Time Frame
Baseline and week 6
Title
Change in Visual Analogue Scale (VAS)
Description
Visual Analogue Scale (VAS) measures pain on a scale from 0 to 10
Time Frame
Baseline and week 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 21-80 years with first-ever clinical stroke diagnosed on CT or MRI brain imaging. Stroke duration of 3-24 months. Stroke type: ischemic or haemorrhagic Fugl-Meyer motor score of the upper limb range from 10-50 Ability to pay attention and maintain supported sitting for 1.5 hours continuously Able to give own consent and understand simple instructions Fulfils BCI resting brain states on initial screening. Exclusion Criteria: Recurrent clinical stroke Functional status: severe aphasia or inattention, unstable medical conditions which may affect participation (e.g. unresolved sepsis, postural hypotension, end stage renal failure) or anticipated life expectancy of <1 year due to malignancy or neurodegenerative disorder) Hemispatial neglect (visual or sensory) or severe visual impairment despite visual aids History of epilepsy, severe depression or active psychiatric disorder Skull defect or previous cranial surgery as this would affect physical fit of EEG cap interface Local arm factors: severe spasticity Modified Ashworth scale >2 in any region, visual analogue scale (VAS score) >4/10, fixed joint contractures or joint replacements, patients with poor skin conditions which would contraindicate repetitive arm training. TMS contraindications: females with reproductive potential not on reliable contraception; pregnancy; cardiac pacemakers; orthodontics (braces); metal implants.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen S Chua, MBBS, FRCP
Organizational Affiliation
Tan Tock Seng Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tan Tock Seng Hospital
City
Singapore
ZIP/Postal Code
308433
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No

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A Study of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for Stroke

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