Parkinson's Disease Clinical Trials

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Observational Study for the Functional Characterization of the Population Diagnosed With Parkinson's Disease in Galicia, and Validation of the Short Physical Performance Battery in Individuals Diagnosed With Parkinson's Disease

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

Parkinson's disease (PD) is a progressive neurodegenerative disorder associated with motor and non-motor impairments that affect physical function, mobility, balance, and quality of life. Although Galicia is one of the Spanish regions with a high prevalence of PD, comprehensive information regarding the functional characteristics of this population remains limited. This observational cross-sectional study aims to characterize the sociodemographic, clinical, cognitive, behavioral, and functional profile of individuals with Parkinson's disease in Galicia and to evaluate the validity and reliability of the Short Physical Performance Battery (SPPB) in this population. The findings will provide updated information on the functional status of people with PD in Galicia and support the use of the SPPB as a practical tool for the assessment of physical performance in clinical and research settings.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Clinical diagnosis of Parkinson's disease confirmed by a neurologist.

• Provision of written informed consent by the participant or, when applicable, by a legally authorized representative.

Locations
Other Locations
Spain
Asociación de Parkinson de la Provincia de Pontevedra
RECRUITING
Pontevedra
Facultad de Fisioterapia
RECRUITING
Pontevedra
Contact Information
Primary
Irimia Mollinedo-Cardalda, PT, PhD
imollinedo@uvigo.es
+34986801771
Backup
Esther Monge-Pereira, PT, PhD
esther.monge@uvigo.es
+34986801750
Time Frame
Start Date: 2026-08-01
Estimated Completion Date: 2026-12-25
Participants
Target number of participants: 350
Related Therapeutic Areas
Sponsors
Leads: University of Vigo

This content was sourced from clinicaltrials.gov