Personalized neurorehabilitative precision medicine: from data to therapies (MWKNeuroReha) - a multi-centre prospective observational clinical trial to predict long-term outcome of patients with acute motor stroke.


Journal

BMC neurology
ISSN: 1471-2377
Titre abrégé: BMC Neurol
Pays: England
ID NLM: 100968555

Informations de publication

Date de publication:
30 Jun 2022
Historique:
received: 06 03 2022
accepted: 17 06 2022
entrez: 30 6 2022
pubmed: 1 7 2022
medline: 6 7 2022
Statut: epublish

Résumé

Stroke is one of the most frequent diseases, and half of the stroke survivors are left with permanent impairment. Prediction of individual outcome is still difficult. Many but not all patients with stroke improve by approximately 1.7 times the initial impairment, that has been termed proportional recovery rule. The present study aims at identifying factors predicting motor outcome after stroke more accurately than before, and observe associations of rehabilitation treatment with outcome. The study is designed as a multi-centre prospective clinical observational trial. An extensive primary data set of clinical, neuroimaging, electrophysiological, and laboratory data will be collected within 96 h of stroke onset from patients with relevant upper extremity deficit, as indexed by a Fugl-Meyer-Upper Extremity (FM-UE) score ≤ 50. At least 200 patients will be recruited. Clinical scores will include the FM-UE score (range 0-66, unimpaired function is indicated by a score of 66), Action Research Arm Test, modified Rankin Scale, Barthel Index and Stroke-Specific Quality of Life Scale. Follow-up clinical scores and applied types and amount of rehabilitation treatment will be documented in the rehabilitation hospitals. Final follow-up clinical scoring will be performed 90 days after the stroke event. The primary endpoint is the change in FM-UE defined as 90 days FM-UE minus initial FM-UE, divided by initial FM-UE impairment. Changes in the other clinical scores serve as secondary endpoints. Machine learning methods will be employed to analyze the data and predict primary and secondary endpoints based on the primary data set and the different rehabilitation treatments. If successful, outcome and relation to rehabilitation treatment in patients with acute motor stroke will be predictable more reliably than currently possible, leading to personalized neurorehabilitation. An important regulatory aspect of this trial is the first-time implementation of systematic patient data transfer between emergency and rehabilitation hospitals, which are divided institutions in Germany. This study was registered at ClinicalTrials.gov ( NCT04688970 ) on 30 December 2020.

Sections du résumé

BACKGROUND BACKGROUND
Stroke is one of the most frequent diseases, and half of the stroke survivors are left with permanent impairment. Prediction of individual outcome is still difficult. Many but not all patients with stroke improve by approximately 1.7 times the initial impairment, that has been termed proportional recovery rule. The present study aims at identifying factors predicting motor outcome after stroke more accurately than before, and observe associations of rehabilitation treatment with outcome.
METHODS METHODS
The study is designed as a multi-centre prospective clinical observational trial. An extensive primary data set of clinical, neuroimaging, electrophysiological, and laboratory data will be collected within 96 h of stroke onset from patients with relevant upper extremity deficit, as indexed by a Fugl-Meyer-Upper Extremity (FM-UE) score ≤ 50. At least 200 patients will be recruited. Clinical scores will include the FM-UE score (range 0-66, unimpaired function is indicated by a score of 66), Action Research Arm Test, modified Rankin Scale, Barthel Index and Stroke-Specific Quality of Life Scale. Follow-up clinical scores and applied types and amount of rehabilitation treatment will be documented in the rehabilitation hospitals. Final follow-up clinical scoring will be performed 90 days after the stroke event. The primary endpoint is the change in FM-UE defined as 90 days FM-UE minus initial FM-UE, divided by initial FM-UE impairment. Changes in the other clinical scores serve as secondary endpoints. Machine learning methods will be employed to analyze the data and predict primary and secondary endpoints based on the primary data set and the different rehabilitation treatments.
DISCUSSION CONCLUSIONS
If successful, outcome and relation to rehabilitation treatment in patients with acute motor stroke will be predictable more reliably than currently possible, leading to personalized neurorehabilitation. An important regulatory aspect of this trial is the first-time implementation of systematic patient data transfer between emergency and rehabilitation hospitals, which are divided institutions in Germany.
TRIAL REGISTRATION BACKGROUND
This study was registered at ClinicalTrials.gov ( NCT04688970 ) on 30 December 2020.

Identifiants

pubmed: 35773640
doi: 10.1186/s12883-022-02759-2
pii: 10.1186/s12883-022-02759-2
pmc: PMC9245298
doi:

Banques de données

ClinicalTrials.gov
['NCT04688970']

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

238

Subventions

Organisme : Ministerium für Wissenschaft, Forschung und Kunst Baden-Württemberg
ID : 42-5400/75/1

Informations de copyright

© 2022. The Author(s).

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Auteurs

Corinna Blum (C)

Department for Neurology & Stroke, University Hospital of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
Hertie Institute for Clinical Brain Research, Ottfried-Müller-Straße 25, 72076, Tübingen, Germany.

David Baur (D)

Department for Neurology & Stroke, University Hospital of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
Hertie Institute for Clinical Brain Research, Ottfried-Müller-Straße 25, 72076, Tübingen, Germany.

Lars-Christian Achauer (LC)

medical Data Integration Centre (meDIC), University Hospital of Tübingen, Schaffhausenstr. 77, 72072, Tübingen, Germany.

Philipp Berens (P)

University Hospital of Tübingen, Institute for Ophthalmic Research, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Germany.
Cluster of Excellence Machine Learning, University of Tübingen, Maria-von-Linden-Str. 6, 72076, Tübingen, Germany.

Stephanie Biergans (S)

medical Data Integration Centre (meDIC), University Hospital of Tübingen, Schaffhausenstr. 77, 72072, Tübingen, Germany.

Michael Erb (M)

Department for Biomedical Magnetic Resonance, University Hospital of Tübingen, Ottfried-Müller-Str. 51, 72076, Tübingen, Germany.
Max Planck Institute for Biological Cybernetics, Max-Planck-Ring 8-14, 72076, Tübingen, Germany.

Volker Hömberg (V)

SRH Gesundheitszentrum Bad Wimpfen GmbH, Bei der alten Saline 2, 74206, Bad Wimpfen, Germany.

Ziwei Huang (Z)

University Hospital of Tübingen, Institute for Ophthalmic Research, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Germany.

Oliver Kohlbacher (O)

medical Data Integration Centre (meDIC), University Hospital of Tübingen, Schaffhausenstr. 77, 72072, Tübingen, Germany.
University hospital of Tübingen, Institute for translational Bioinformation (TBI), Schaffhausenstr. 77, 72072, Tübingen, Germany.
University of Tübingen, Interfaculty Institute for Biomedical Informatics (IBMI), Sand 14, 72076, Tübingen, Germany.
Department of Computer Science, Applied Bioinformatics (ABI), University of Tübingen, Sand 14, 72076, Tübingen, Germany.

Joachim Liepert (J)

Schmieder Clinic Allensbach, Zum Tafelholz 8, 78476, Allensbach, Germany.

Tobias Lindig (T)

Department for Diagnostic and Interventional Neuroradiology, University Hospital of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.

Gabriele Lohmann (G)

Department for High-field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max-Planck-Ring 11, 72076, Tübingen, Germany.

Jakob H Macke (JH)

Cluster of Excellence Machine Learning, University of Tübingen, Maria-von-Linden-Str. 6, 72076, Tübingen, Germany.

Jörg Römhild (J)

medical Data Integration Centre (meDIC), University Hospital of Tübingen, Schaffhausenstr. 77, 72072, Tübingen, Germany.

Christine Rösinger-Hein (C)

Hertie Institute for Clinical Brain Research, Ottfried-Müller-Straße 25, 72076, Tübingen, Germany.

Brigitte Zrenner (B)

Department for Neurology & Stroke, University Hospital of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
Hertie Institute for Clinical Brain Research, Ottfried-Müller-Straße 25, 72076, Tübingen, Germany.

Ulf Ziemann (U)

Department for Neurology & Stroke, University Hospital of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany. ulf.ziemann@uni-tuebingen.de.
Hertie Institute for Clinical Brain Research, Ottfried-Müller-Straße 25, 72076, Tübingen, Germany. ulf.ziemann@uni-tuebingen.de.

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