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Rehabilitation of Stroke Patients for Maximal Neurological Restoration

Training the Surviving Neural Network to Create New Synaptic Connections That Can Maximize Restoration of Motor Functions After Stroke

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05086055
Acronym
PROTEQT
Enrollment
200
Registered
2021-10-20
Start date
2021-11-11
Completion date
2024-02-29
Last updated
2023-11-30

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

Conditions

Stroke

Keywords

Rehabilitation

Brief summary

Multimodal imaging of stroke patients. Patients included in the study will be investigated with multiparametric imaging tools including MRI and EEG imaging. Improvements in motor skills will be monitored clinically.

Detailed description

We aim to (i) quantify the size of the brain lesion and assess the surviving functional neural network connections; (ii) Analyze the type and degree of inflammation initiated by the stroke-induced brain lesion. We will stratify inflammation according to lesion volume, surviving functional neural network connections, age, NIHSS and Modified Rankin Scale (mRS) and analyze how inflammation markers change during rehabilitation; (iii) Train the surviving neural network to create new synaptic connections that can maximize restoration of motor functions; (iv) Apply and develop advanced mathematical and computational methods to model and predict how stroke rehabilitation can rewire the neural network connections to best facilitate restoration of lost motor function.

Interventions

BEHAVIORALKinematic movement analysis

moving arm/leg while registration with electromyography, electroencephalogram, accelerometers, functional near infrared spectroscopy and 3 dimensional video registration of hand, arm, foot and leg movements.

Sponsors

St. Olavs Hospital
CollaboratorOTHER
OsloMet
CollaboratorUNKNOWN
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* subcortical strokes resulting in arm motor deficits. * admitted to the stroke unit, St Olav´s Hospital during 2021-2023

Exclusion criteria

* Previous stroke * neurodegenerative disease * brain tumors * previous neurotrauma or brain operation * aphasia * cognitive dysfunction and claustrophobia preventing MRI examinations.

Design outcomes

Primary

MeasureTime frameDescription
Changes in brain volume6 monthsStroke induced brain volume changes (mm3) will be measured using magnetic resonance imaging (MRI) at 1 day and 6 months post-stroke.
Stroke induced changes in brain activity.6 monthsDocument longitudinal changes in brain activity using EEG. Changes will be measured in cycles/second (Hertz, Hz).
Changes in inflammatory activity in brain6 monthsMarkers of post-stroke inflammation will be measured in pg/ml and ng/ml.
muscle function6 monthsLongitudinal kinematic profiling. Electromyography measurements of muscle function post-stroke will be measured in cycles/second (Hz) and amplitude (mm). Extension and flexion of arm will be measured in cm. Joint angles will be measured in degrees. Speed of flexion and extension will be measured in cm/second

Countries

Norway

Contacts

Primary ContactAxel Sandvig, PhD ass prof
axel.sandvig@ntnu.no+46 72575620

Outcome results

None listed

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