Background Stroke is a leading cause of long-term disability worldwide. Neuromuscular electrical stimulation (NMES), such as the geko™ device, may enhance cerebral perfusion post-stroke by improving venous return. This study evaluated the cortical haemodynamic effects of NMES in subacute stroke survivors using functional near-infrared spectroscopy (fNIRS).
Methods A prospective observational study was conducted in 18 patients (>7 days post-ischaemic stroke) receiving bilateral lower limb NMES. fNIRS measured changes in oxyhaemoglobin (HbO) and deoxyhaemoglobin (HbR) concentrations across varying NMES intensities and postures (supine, semi-supine, and upright). Data were analysed using a general linear model, with β-values reflecting haemodynamic response magnitude.
Results NMES evoked significant cortical haemodynamic responses, with increased HbO observed across multiple sensorimotor regions. Upright posture significantly enhanced cortical tissue oxygenation (p=0.010). Higher stimulation intensities produced greater HbO responses, indicating a dose-dependent effect. Larger infarct size (>5 cm) was associated with increased haemodynamic response. These findings suggest NMES may influence neurovascular coupling and cerebral autoregulation during stroke recovery.
Conclusions NMES via the geko™ device enhances cortical oxygenation in subacute stroke, particularly in upright positions and at higher intensities. The results support the potential use of NMES not only for venous thromboembolism prevention but also as an adjunctive strategy to promote cerebral perfusion and facilitate rehabilitation. Further trials are warranted to explore clinical efficacy and functional outcomes.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialNCT06614400
Funding StatementThis work was supported by Innovate UK (Application No: 10038715) funding to Firstkind Ltd. who had no role in study design, data analysis, interpretation, or manuscript preparation.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The study was conducted in accordance with the Declaration of Helsinki and was approved by the local Research Ethics Committee (REC reference number: 343056) at the Stroke Rehabilitation Unit at Ellesmere Port Hospital, Chester, UK.
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
FootnotesStatements and Declarations: This work was supported by Innovate UK (Application No: 10038715) funding to Firstkind Ltd. who had no role in study design, data analysis, interpretation, or manuscript preparation. The authors declare no commercial or financial relationships that could be construed as a potential conflict of interest.
Data AvailabilityThe statistical results analysed during the current study are available in the supplementary materials.
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