Skip to content

Post-stroke hand rehabilitation with MEG-based brain-robot interface

M/EEG based Post-stroke Neurorehabilitation with Brain-Robot Interface

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN88026375
Enrollment
30
Registered
2020-11-24
Start date
2020-10-07
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Neurorehabilitation of chronic stroke patients Nervous System Diseases

Interventions

A therapy session normally consists of approximately half an hour of physical (i.e. motor execution (ME)) practice followed by half an hour of motor imagery (MI) practice. This amounts to 4 runs of PP

Sponsors

University of Ulster
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Post-stroke volunteers aged 18 - 80 years with normal or corrected to normal vision (e.g. normal vision by using glasses) 2. 6 months - 2 years post-stroke since first episode of stroke 3. Able to follow two-part spoken or written commands 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. Prepared to remove all body piercings

Exclusion criteria

Exclusion criteria: 1. Known to have a progressive neurological condition 2. Have metal or active implants in their body (excluding dental fillings or crowns) 3. Known to suffer from claustrophobia 4. Pregnant or breast feeding 5. Gross cognitive impairment or disorientation, evidenced by a Hodgkinson mini-mental test score (HMMS) (Hodgkinson, 1972) of less than 21/30

Design outcomes

Primary

MeasureTime frame
1. Functional recovery measured using the Action Research Arm Test (ARAT) and grip strength on a weekly basis during the trial period 2. Functional connectivity among activated brain regions will be computed using activation related MEG/EEG-EMG data on a weekly basis during the trial period

Secondary

MeasureTime frame
1. Participants’ mood, motivation, and fatigue levels will be continuously monitored during sessions using appropriate methods including visual analog scales 2. Mood will be assessed weekly, using the Centre for Epidemiologic Studies-Depression Scale

Countries

Ireland, Northern Ireland, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026