Skip to content

Effect of EEG-EMG based hybrid brain-computer interface operated hand exoskeleton for poststroke hand functional recovery

A BCI operated hand exoskeleton based neuro-rehabilitation system for movement restoration in paralysis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13139098
Enrollment
20
Registered
2018-06-22
Start date
2017-04-12
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Chronic stroke patients suffering from post-stroke hand plegia on either side of the body (left/right) Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

Participants underwent hand therapy sessions with a frequency of 1-3 times/week, for a period of 6-8 weeks. Each therapy session consists of a 30 min long Physical Practice (PP) mediated by a hand exo

Sponsors

UKIERI
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Male and female post-stroke volunteers, in the age group of 18-80 years and have normal or corrected to normal vision (e.g. normal vision by using glasses) 2. Six months – two years post-stroke since the first episode of stroke: this is to capture stroke survivors within the chronic stage and also to ensure the stage of fast spontaneous recovery has finished 3. Able to follow two-part spoken or written commands: this is to ensure stroke survivors can provide informed consent and also to ensure they will be able to comply with therapy 4. Have movement disability in at least one of their hands due to stroke 5. Able to get in and out of a low seat unassisted 6. Ready to remove all body piercings

Exclusion criteria

Exclusion criteria: 1. Aged less than 18 years or above 80 years 2. Known to have a progressive neurological condition, any serious medical or psychological diseases which are likely to seriously affect their ability to continue with experimentation 3. Have metal or active implants in their body (excluding dental fillings or crowns) 4. Known to suffer from claustrophobia 5. Pregnant or breastfeeding 6. Gross cognitive impairment or disorientation, evidenced by a score of <21 in the Mini-Mental State Examination (MMSE); the MMSE is an 11-item reliable and valid measure of cognitive function (Folstein, Folstein & McHugh 1975), such that they are unable to follow verbal or written instruction

Design outcomes

Primary

MeasureTime frame
Hand functional recovery measured using action research arm test (ARAT) and the grip-strength (GS) measurement on a weekly basis for a period of 6-8 weeks

Secondary

MeasureTime frame
Motivation and fatigue measured using the visual analog scale (0-10 cm) before and after each therapy session

Countries

Northern Ireland, United Kingdom

Contacts

Public ContactGirijesh Prasad
g.prasad@ulster.ac.uk+44 (0)28 7167 5645

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 17, 2026