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

A Pilot Feasibility Clinical Trial of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for postStroke Arm Paresis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02765334
Acronym
nBETTER
Enrollment
13
Registered
2016-05-06
Start date
2015-12-28
Completion date
2017-08-16
Last updated
2018-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

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.

Interventions

DEVICEnBETTER

60 minutes of nBETTER training followed by 30 minutes of conventional therapy occupational therapy. Total of 18 sessions over 6 weeks.

Sponsors

Institute for Infocomm Research
CollaboratorOTHER
National University Hospital, Singapore
CollaboratorOTHER
Tan Tock Seng Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Intervention model description

Feasibility of nBETTER training (60 minutes) with conventional arm therapy (30minutes) for chronic stroke.

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Upper extremity Fugl-Meyer motor score post trainingBaseline and week 6As above

Secondary

MeasureTime frameDescription
Change in Transcranial Magnetic Stimulation Assessment (TMS)Baseline and week 6As above
Change in Grip StrengthBaseline and week 6Grip Strength measures hand force in kgf
Change in Frenchay Arm Test of Function (FAT)Baseline and week 6Frenchay 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)Baseline and week 6Modified 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)Baseline and week 6Visual Analogue Scale (VAS) measures pain on a scale from 0 to 10

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026