Evidence map›Paper›PMID 40968373›Full record

ArticleNeurological research and practice2025

Consensus on the clinical utility of digital mobility outcomes for personalized clinical decision support in parkinson's disease.

Alan Castro Mejia, Stefano Sapienza, Ivana Paccoud, Lisa Alcock, Philip Brown, Heiko Gaßner, Heather Hunter, Walter Maetzler, Anat Mirelman, Alice Nieuwboer and 6 more

Abstract read
In one paragraph

Article in Neurological research and practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Alan Castro Mejia *Luxembourg Centre for Systems Biomedicine, Digital Medicine Group, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Stefano Sapienza *Luxembourg Centre for Systems Biomedicine, Digital Medicine Group, University of Luxembourg, Esch-sur-Alzette, Luxembourg. stefano.sapienza@uni.lu.ORCID http://orcid.org/0000-0002-0917-6454
Ivana PaccoudLuxembourg Centre for Systems Biomedicine, Digital Medicine Group, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Lisa AlcockNIHR Newcastle Biomedical Research Centre, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Philip BrownThe Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Heiko GaßnerDepartment of Molecular Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Heather HunterThe Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Walter MaetzlerDepartment of Neurology, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.
Anat MirelmanLaboratory for Early Markers of Neurodegeneration (LEMON), Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Alice NieuwboerNeurorehabilitation Research Group (eNRGy), Department of Rehabilitation Sciences, KU Leuven, Leuven, Vlaams-Brabant, Belgium.
Martin RegensburgerDepartment of Molecular Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Lynn RochesterNIHR Newcastle Biomedical Research Centre, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Sabine StallforthDepartment of Molecular Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Beatrix VereijkenDepartment of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway.
Alison YarnallNIHR Newcastle Biomedical Research Centre, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Jochen KluckenLuxembourg Centre for Systems Biomedicine, Digital Medicine Group, University of Luxembourg, Esch-sur-Alzette, Luxembourg.

Funding

Deutsche Forschungsgemeinschaft 438496663Deutsche Forschungsgemeinschaft 442419336Fonds National de la Recherche Luxembourg 14146272Fonds National de la Recherche Luxembourg 17981757Fraunhofer Internal Programs 044-602140Fraunhofer Internal Programs 044-602150Fraunhofer Internal Programs SME 40-09311Innovative Medicines Initiative 820820NIHR Newcastle Biomedical Research Centre 2020-2024; 2024-2028
6 · The paper itself

Abstract

backgroundDigital mobility outcomes (DMOs) have emerged as novel biomarkers offering objective, quantitative, and examiner-independent outcome measures for clinical studies. Unfortunately, research efforts on DMOs have not yet investigated the domain of clinical utility in Parkinson's disease, i.e. providing evidence of improvements in health outcomes, diagnosis, decision-making, or prevention when compared to e.g. standard-of-care procedures. This manuscript, via a consensus building approach, aims to create a structured conceptual framework to map the knowledge generated by DMOs with clinical domains that could benefit from it.

methodsWe conducted a three-round consensus-building study with 12 experts recruited from the Mobilise-D consortium's Parkinson's Disease Working Group. The experts designed and ranked different aspects of the conceptual framework via a 5-level Likert scale for level of agreement. Consensus for the different points evaluated was based on a double threshold: the simultaneous presence of a high level of agreement had to be accompanied by a low level of disagreement. As secondary objectives, the experts were asked to rate the practical application of DMOs by evaluating the timeline to applicability, the foreseen challenges for their implementation in clinical settings, and their main role in the decision-making process.

resultsA full consensus on the clinical utility framework was achieved after three rounds. The final framework consisted of three main categories (Disease Diagnosis, Patient Evaluation, and Treatment Evaluation) and six underlying domains (Enhancing Diagnostic Procedure, Predicting Risk, Timely Detecting Deterioration, Enhancing Clinical Judgment, Selecting Treatment, and Monitoring Treatment Response). The experts believed in the next 1-5 years DMOs will play a relevant role in clinical decision making, complementing care knowledge with useful digital biomarkers information. However, the main challenge to address is the definition of clear reference value for DMOs interpretability.

conclusionsThis framework provides a structure for subsequent studies to build into by diversifying expert cohorts and expand our findings beyond PD. Additionally, our results support researchers planning future clinical trials where DMOs can play a valuable role for clinical decision support. Ultimately, this is the first step toward developing guidelines to assess DMOs' clinical utility and support their integration into Real World clinical practice.

Indexed as

Clinical utilityConsensus studyDigital mobility outcomesGaitParkinson’s disease

Identifiers

PMID40968373
PMCPMC12447593

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.