Beyond protocol standardization: The importance of data curation and software transparency
Mancini et al.'s framework for gait assessment in Parkinson's disease (PD) is a valuable contribution, enabling a harmonization of study protocols in this research field and, consequently, a substantial improvement of data interpretation across different cohorts. However, we believe that r...
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Published in | Journal of Parkinson's disease p. 1877718X251377876 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
18.09.2025
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Subjects | |
Online Access | Get full text |
ISSN | 1877-7171 1877-718X |
DOI | 10.1177/1877718X251377876 |
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Abstract | Mancini et al.'s framework for gait assessment in Parkinson's disease (PD) is a valuable contribution, enabling a harmonization of study protocols in this research field and, consequently, a substantial improvement of data interpretation across different cohorts. However, we believe that recommendations concerning data curation and software use should be provided in more detail. To ensure data interoperability and facilitate robust data aggregation from such protocols, appropriate and harmonized data formatting and metadata standards are necessary. We further advocate for the open sharing of gait analysis algorithms, to enhance reproducibility and foster collaborative development.
Why Data Sharing and Open Software Matter for Parkinson's Gait Studies
Plain Language Summary:
Understanding how Parkinson's disease affects gait is important for improving diagnosis and treatment. A recent study suggested that researchers should use the same protocol when studying walking in people with Parkinson's disease. This would help scientists compare and combine their results more easily, making research more reliable. While this is a great step forward, we believe it is also important to focus on how the data from these studies is handled and shared. This includes making sure the data is clearly organized, stored in standard formats, and described with helpful background information (called metadata). These steps make it easier for different researchers to use the data together. We also recommend that researchers share algorithms they use to analyze the data. When these tools are openly available, it is easier to doublecheck results and build better tools through teamwork. Overall, better data practices and open sharing of software can help speed up progress in Parkinson's research and lead to better outcomes for people living with the disease. |
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AbstractList | Mancini et al.'s framework for gait assessment in Parkinson's disease (PD) is a valuable contribution, enabling a harmonization of study protocols in this research field and, consequently, a substantial improvement of data interpretation across different cohorts. However, we believe that recommendations concerning data curation and software use should be provided in more detail. To ensure data interoperability and facilitate robust data aggregation from such protocols, appropriate and harmonized data formatting and metadata standards are necessary. We further advocate for the open sharing of gait analysis algorithms, to enhance reproducibility and foster collaborative development. Mancini et al.'s framework for gait assessment in Parkinson's disease (PD) is a valuable contribution, enabling a harmonization of study protocols in this research field and, consequently, a substantial improvement of data interpretation across different cohorts. However, we believe that recommendations concerning data curation and software use should be provided in more detail. To ensure data interoperability and facilitate robust data aggregation from such protocols, appropriate and harmonized data formatting and metadata standards are necessary. We further advocate for the open sharing of gait analysis algorithms, to enhance reproducibility and foster collaborative development. Why Data Sharing and Open Software Matter for Parkinson's Gait Studies Plain Language Summary: Understanding how Parkinson's disease affects gait is important for improving diagnosis and treatment. A recent study suggested that researchers should use the same protocol when studying walking in people with Parkinson's disease. This would help scientists compare and combine their results more easily, making research more reliable. While this is a great step forward, we believe it is also important to focus on how the data from these studies is handled and shared. This includes making sure the data is clearly organized, stored in standard formats, and described with helpful background information (called metadata). These steps make it easier for different researchers to use the data together. We also recommend that researchers share algorithms they use to analyze the data. When these tools are openly available, it is easier to doublecheck results and build better tools through teamwork. Overall, better data practices and open sharing of software can help speed up progress in Parkinson's research and lead to better outcomes for people living with the disease. |
Author | Welzel, Julius Jeung, Sein Maetzler, Walter Cockx, Helena Hansen, Clint Romijnders, Robbin Jacobsen, Nadine Wollesen, Bettina |
Author_xml | – sequence: 1 givenname: Julius orcidid: 0000-0001-8958-0934 surname: Welzel fullname: Welzel, Julius organization: Department of Neurology, University Hospital Schleswig-Holstein Campus Kiel and Kiel University, Kiel, Germany, Neuropsychology Lab, Department of Psychology, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany – sequence: 2 givenname: Nadine orcidid: 0000-0001-6612-7328 surname: Jacobsen fullname: Jacobsen, Nadine organization: Neuropsychology Lab, Department of Psychology, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany – sequence: 3 givenname: Helena orcidid: 0000-0001-7782-7178 surname: Cockx fullname: Cockx, Helena organization: Department of Neurology, Center of Expertise for Parkinson and Movement Disorders, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, Netherlands – sequence: 4 givenname: Sein orcidid: 0000-0002-0247-087X surname: Jeung fullname: Jeung, Sein organization: Department of Biopsychology and Neuroergonomics, Technische Universität Berlin, Berlin, Germany – sequence: 5 givenname: Robbin orcidid: 0000-0002-2507-0924 surname: Romijnders fullname: Romijnders, Robbin organization: Department of Neurology, University Hospital Schleswig-Holstein Campus Kiel and Kiel University, Kiel, Germany – sequence: 6 givenname: Clint orcidid: 0000-0003-4813-3868 surname: Hansen fullname: Hansen, Clint organization: Department of Neurology, University Hospital Schleswig-Holstein Campus Kiel and Kiel University, Kiel, Germany – sequence: 7 givenname: Bettina orcidid: 0000-0002-1082-9141 surname: Wollesen fullname: Wollesen, Bettina organization: Institute for Movement Therapy and Movement-oriented Prevention and Rehabilitation, German Sports University Cologne, Cologne, Germany – sequence: 8 givenname: Walter orcidid: 0000-0002-5945-4694 surname: Maetzler fullname: Maetzler, Walter organization: Department of Neurology, University Hospital Schleswig-Holstein Campus Kiel and Kiel University, Kiel, Germany |
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