Effects of basic and dual-task training programs on physical function in Parkinson’s disease: The PARKEX study
12 affiliations
- 1Universitat Ramon Llull, Facultat de Psicologia, Ciències de l’Educació i de l’Esport Blanquerna, Barcelona, Spain
- 2Grup de Malalties Neurodegeneratives de la Vall d’Hebron. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain
- 3MIA-Portugal, Multidisciplinary Institute of Ageing, University of Coimbra, Coimbra, Portugal
- 4CIBB, Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, Portugal
- 5UCIBIO, Applied Molecular Biosciences Unit, Department of Chemistry, Faculty of Science and Technology, NOVA University Lisbon, Caparica, Portugal
- 6Associate Laboratory i4HB-Institute for Health and Bioeconomy, Faculty of Science and Technology, NOVA University Lisbon, Caparica, Portugal
- 7Hospital Nostra Senyora de Meritxell, Escaldes-Engordany, Andorra
- 8Universitat d’Andorra, Sant Julià de Lòria, Andorra
- 9Aligning Science Across Parkinson’s (ASAP) Collaborative Research NetworkChevy Chase, Maryland, United States of America
- 10Institut de Neurociències-Autonomous Universitat de Barcelona (INc-UAB), Cerdanyola del Vallès, Spain
- 11Universitat Ramon Llull, Facultat de Ciències de la Salut Blanquerna, Barcelona, Spain
- 12Departament de Neurologia. Hospital Universitari Vall D’Hebron, Barcelona, Spain
Abstract
Exercise is a promising non-pharmacological intervention for motor and non-motor symptoms in Parkinson’s disease (PD). However, direct comparisons between basic physical training (BPT) and dual-task training remain limited. The objective of the current clinical trial is to evaluate clinical and functional effects of BPT and a BPT combined with dual-task functional exercises (BPT + FE) in individuals with PD. In this randomized controlled trial, 24 participants with idiopathic PD were allocated to BPT, BPT + FE, or a no-intervention control group (Con). Interventions lasted 12 weeks (three 60-minute sessions/week). Outcomes included quality of life (PDQ-39), depressive symptoms (BDI), lower-limb strength (1-minute Sit-to-Stand Test, STS), and functional mobility (Timed Up and Go, TUG). Group effects were analyzed using permutation-based ANOVA with Bonferroni correction. Both interventions significantly improved physical performance vs. controls. STS gains were observed for BPT vs. Con (Mean Difference, MD = 31.00; p = .0026) and BPT + FE vs. Con (MD = 19.00; p = .0026). TUG times improved for BPT vs. Con (MD = –2.07s; p = .0039) and BPT + FE vs. Con (MD = –2.43s; p = .0028). Although BDI and PDQ-39 did not show statistically significant changes between group differences (r_rb = –0.429 and –0.339, respectively), several subscales demonstrated medium effect sizes suggesting potentially meaningful trends: emotional well-being (BPT: r_rb = –0.428; BPT + FE: r_rb = –0.446), bodily discomfort (BPT: r_rb = –0.524), and activities of daily living (BPT + FE: r_rb = –0.429). In conclusion, both programs improved physical performance in PD. Patient-reported outcomes did not reach statistical significance, but effect-size patterns suggest possible psychosocial benefits that warrant confirmation in larger trials. Trial registration ClinicalTrials.gov, NCT05963425.
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BibTeX
@article{magana2026effects,
title = {{Effects of basic and dual-task training programs on physical function in Parkinson’s disease: The PARKEX study}},
author = {Juan Carlos Magaña and Silvia Enríquez-Calzada and Roger Prat and Cláudia M. Deus and Susana P. Pereira and Mercè Avellanet and Elvira Gea and Ariadna Laguna and Marta Martinez-Vicente and Ona Perez-Larumbe and Maria Giné-Garriga and Jorge Hernández-Vara and Joel Montane},
journal = {PLOS One},
year = {2026},
month = sep,
doi = {10.1371/journal.pone.0358534},
url = {https://doi.org/10.1371/journal.pone.0358534},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Effects of basic and dual-task training programs on physical function in Parkinson’s disease: The PARKEX study
AU - Juan Carlos Magaña
AU - Silvia Enríquez-Calzada
AU - Roger Prat
AU - Cláudia M. Deus
AU - Susana P. Pereira
AU - Mercè Avellanet
AU - Elvira Gea
AU - Ariadna Laguna
AU - Marta Martinez-Vicente
AU - Ona Perez-Larumbe
AU - Maria Giné-Garriga
AU - Jorge Hernández-Vara
AU - Joel Montane
PY - 2026
DA - 2026/09/18
JO - PLOS One
DO - 10.1371/journal.pone.0358534
UR - https://doi.org/10.1371/journal.pone.0358534
AB - Exercise is a promising non-pharmacological intervention for motor and non-motor symptoms in Parkinson’s disease (PD). However, direct comparisons between basic physical training (BPT) and dual-task training remain limited. The objective of the current clinical trial is to evaluate clinical and functional effects of BPT and a BPT combined with dual-task functional exercises (BPT + FE) in individuals with PD. In this randomized controlled trial, 24 participants with idiopathic PD were allocated to BPT, BPT + FE, or a no-intervention control group (Con). Interventions lasted 12 weeks (three 60-minute sessions/week). Outcomes included quality of life (PDQ-39), depressive symptoms (BDI), lower-limb strength (1-minute Sit-to-Stand Test, STS), and functional mobility (Timed Up and Go, TUG). Group effects were analyzed using permutation-based ANOVA with Bonferroni correction. Both interventions significantly improved physical performance vs. controls. STS gains were observed for BPT vs. Con (Mean Difference, MD = 31.00; p = .0026) and BPT + FE vs. Con (MD = 19.00; p = .0026). TUG times improved for BPT vs. Con (MD = –2.07s; p = .0039) and BPT + FE vs. Con (MD = –2.43s; p = .0028). Although BDI and PDQ-39 did not show statistically significant changes between group differences (r_rb = –0.429 and –0.339, respectively), several subscales demonstrated medium effect sizes suggesting potentially meaningful trends: emotional well-being (BPT: r_rb = –0.428; BPT + FE: r_rb = –0.446), bodily discomfort (BPT: r_rb = –0.524), and activities of daily living (BPT + FE: r_rb = –0.429). In conclusion, both programs improved physical performance in PD. Patient-reported outcomes did not reach statistical significance, but effect-size patterns suggest possible psychosocial benefits that warrant confirmation in larger trials. Trial registration ClinicalTrials.gov, NCT05963425.
SN - 1932-6203
ER -