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Recruiting NCT06907589

NCT06907589 A Novel Accessible and Widespread Healthcare Service Model Based on Technology Innovation for Objective (Early) Diagnosis and Therapeutic Monitoring of Parkinson's Disease Promoting Continuity of Care

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Clinical Trial Summary
NCT ID NCT06907589
Status Recruiting
Phase
Sponsor Scuola Superiore di Studi Universitari e di Perfezionamento Sant'Anna
Condition Parkinson Disease
Study Type INTERVENTIONAL
Enrollment 250 participants
Start Date 2024-05-13
Primary Completion 2026-01

Eligibility & Interventions

Sex All sexes
Min Age 50 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Motor Data Analysis

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 250 participants in total. It began in 2024-05-13 with a primary completion date of 2026-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The present study aims to use the SensMode System - a system composed of wearable devices for upper and lower limb movement analysis and electronic device for data acquisition and processing - on healthy subjects, subjects with idiopathic hyposmia, patients with Parkinson's disease, and subjects with de-novo drug-naïve extrapyramidal syndrome. The purpose is to identify normative data of objective motor measures obtained with such a system, as well as to increase knowledge about the potential contribution such a solution can make to the preclinical diagnosis of Parkinson's disease and the management of patients with this disease.

Eligibility Criteria

Inclusion Criteria: 1. Healthy subjects - Inclusion Criteria: * Adult subjects, both sexes, aged 50-80 years old * MMSE score \>= 24 absence of olfactory deficit detected on IOIT olfactory test (22). Age class 50-59 years: normal with score \<=5; age class 60-69 years: normal with score \<=6; age class \> 70 years: normal with score \<=7 * absence of neurological diseases * absence of functional deficit in the sphere of locomotion as a result of traumatic injury or from other cause to the upper and/or lower limbs and/or pelvis and/or spine * expression of informed consent to participate in the study 2. Subjects with Parkinson's disease -- Inclusion criteria: * adult subjects, both sexes, 50-80 years of age * MMSE score \>= 24 * subjects with Parkinson's disease in the absence of motor fluctuations and dyskinesias, or subjects with Parkinson's disease with mild motor fluctuations throughout the day, but to be examined in the ON phase and in the absence of dyskinesias * Hoehn and Yahr stage 1, 2, 3 * absence of functional deficit in the sphere of locomotion as a result of traumatic injury or from other cause to the upper and/or lower limbs and/or pelvis and/or spine * expression of informed consent to participate in the study Exclusion Criteria: 1. Healthy subjects - Exclusion criteria: * denial of informed consent to participate in the study * Presence of olfactory deficit detected on IOIT olfactory test. Age class 50-59 years: hyposmia with score \>=6; age class 60-69 years: hyposmia with score \>=7; age class \> 70 years: hyposmia with score \>=8 * body weight greater than 120 kg * insufficient degree of cooperation * malignant neoplasm in progress or with negative follow-up of less than 6 years * structured joint stiffness in the upper and/or lower extremities preventing proper execution of movements * paresis and/or plegia of upper and/or lower limb muscle groups from both peripheral and central nerve injury * mono/multi/poly sensory and/or motor neuropathy * chronic inflammatory diseases with joint involvement of the upper and/or lower limbs * vertiginous syndromes in the acute phase * neurodegenerative diseases * fever * venous thrombosis * cardiovascular disorders or other acute or chronic conditions capable of affecting the proper performance of motor exercises * spinal or joint pain of various etiologies that may affect the performance of motor exercises * positive history of recurrent acute cervico-brachialgia and/or lumbosciatica 2. Subjects with Parkinson's disease - Exclusion criteria: * Denial of informed consent to participate in the study * Hoenn and Yahr stage 4, 5 * Patient who needs to use an aid (cane or walker) while walking or cannot walk unless aided by a person * body weight greater than 120 kg * insufficient degree of cooperation * malignant neoplasm in place or with negative follow-up of less than 6 years * structured joint stiffness in the upper and/or lower extremities that prevents proper execution of movements * paresis and/or plegia of upper and/or lower limb muscle groups from both peripheral and central nerve injury mono/multi/poly sensory and/or motor neuropathy * chronic inflammatory diseases with joint involvement of the upper and/or lower limbs * vertiginous syndromes in the acute phase * neurodegenerative diseases, excluding Parkinson's disease * fever * venous thrombosis * cardiovascular disorders or other acute or chronic conditions capable of affecting the proper performance of motor exercises * spinal or joint pain of various etiologies that may affect the performance of motor exercises * positive history of recurrent acute cervico-brachialgia and/or low back pain

Contact & Investigator

Central Contact

Filippo Cavallo

✉ filippo.cavallo@santannapisa.it

📞 +390552758663

Frequently Asked Questions

Who can join the NCT06907589 clinical trial?

This trial is open to participants of all sexes, aged 50 Years or older, up to 80 Years, studying Parkinson Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06907589 currently recruiting?

Yes, NCT06907589 is actively recruiting participants. Contact the research team at filippo.cavallo@santannapisa.it for enrollment information.

Where is the NCT06907589 trial being conducted?

This trial is being conducted at Bagno a Ripoli, Italy, Florence, Italy, Florence, Italy, Massa, Italy and 1 additional location.

Who is sponsoring the NCT06907589 clinical trial?

NCT06907589 is sponsored by Scuola Superiore di Studi Universitari e di Perfezionamento Sant'Anna. The trial plans to enroll 250 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology