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- Klinische proef NCT07679256
Integrated Digital and Neurogenic Exosome Biomarkers for Early Diagnosis of Parkinson's Disease: Development and Application
25 juni 2026 bijgewerkt door: Fujian Medical University Union Hospital
Based on the high-quality Parkinson's disease cohort population and biological sample database in the early stage of the team, multi-dimensional intelligent wearable device technology and machine learning were used to screen and classify digital biomarkers in the prodromal PD cohort, early PD cohort and healthy population cohort.
Using peptide nanoprobes, metabolomics and Simoa technology to find the pathological molecular biomarkers of high-purity blood neurogenic exosomes in the prodromal stage of PD cohort, early PD cohort and healthy population cohort, and conduct classification and combination study.
The association analysis was used to explore the specific internal relationship between digital biomarkers and neurogenic exosome molecular biomarkers, to explore the potential relationship between the two types of biomarkers, and to further apply machine learning methods to establish a fusion model for early diagnosis of PD including markers related to digital phenotype and pathological molecular mechanism, and to verify it clinically.
The research results of this project are expected to bring new strategies for the early diagnosis of PD biomarkers, provide theoretical support for clinical transformation, and have important clinical significance for achieving the goal of early diagnosis and early treatment.
Studie Overzicht
Toestand
Werving
Conditie
Studietype
Observationeel
Inschrijving (Geschat)
700
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: qinyong ye
- Telefoonnummer: 13365910205
- E-mail: unionqyye@163.com
Studie Locaties
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Fujian
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Fuzhou, Fujian, China, 350000
- Werving
- Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital
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Contact:
- Department of Neurology, Fujian Institute of Geriatrics, Fujia Department of Neurology, Fujian Institute of Geriatrics, Fujia
- Telefoonnummer: +86 591 8621 8329
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Ja
Bemonsteringsmethode
Kanssteekproef
Studie Bevolking
This study comprises a combined retrospective and prospective cohort of patients with idiopathic Parkinson's disease (PD), selected from the PD registry database maintained by our team at Fujian Medical University Union Hospital.
The study population includes individuals who meet all of the following criteria: (1) diagnosed with idiopathic PD based on the Movement Disorder Society (MDS) clinical diagnostic criteria; (2) Hoehn-Yahr (H-Y) stage ≤ 2.0 during off-medication periods; and (3) Mini-Mental State Examination (MMSE) score > 24 points.
Eligible participants will be identified from the existing database for retrospective data collection, while prospective follow-up data will be collected for the same cohort to enable comprehensive longitudinal analyses.
Beschrijving
Inclusion Criteria:
1. Healthy Control Group
- No severe mental illness;
- Mini-Mental State Examination (MMSE) score >24 points; 2. Prodromal PD Group
- Meets the diagnostic criteria for rapid eye movement sleep behavior disorder;
- Has no severe mental disorders;
- Mini-Mental State Examination (MMSE) score is greater than 24 points. 3. Early PD Group
(1) Diagnosed with idiopathic Parkinson's disease based on the MDS clinical diagnostic criteria ; (3) Hoehn-Yahr (H-Y) stage <=2.0 during off-medication periods; (4) Mini-Mental State Examination (MMSE) score >24 points;
Exclusion Criteria:
- Presence of mental, cognitive, or psychological disorders, unable to sign informed consent;
- Presence of other diseases affecting walking distance, such as lower limb joint lesions, spinal lesions, neurological disorders, or severe cardiopulmonary diseases;
- Presence of intracranial structural changes, cerebrovascular disease, or other neurological disorders;
- Presence of tumors, severe liver or kidney dysfunction (indicators exceeding three times the normal value), or other conditions that significantly impact health;
- Claustrophobia or presence of implants affecting MRI scanning.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
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Gezondheidscontrole
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PD prodromal group
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Early PD group
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Mini-mental State Examination
Tijdsspanne: baseline
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Mini-Mental State Examination (MMSE) is a 30-item cognitive screening tool assessing orientation, memory, attention, calculation, and language, with total scores ranging from 0 to 30.
Higher scores indicate better cognitive function.
Scores ≥27 generally indicate normal cognition, while lower scores suggest varying degrees of impairment, with cutoffs adjusted for education and age.
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baseline
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Montreal Cognitive Assessment
Tijdsspanne: baseline
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Montreal Cognitive Assessment (MoCA) is a 10-15 minute screening tool covering 8 cognitive domains through 12 tasks, with total scores ranging from 0 to 30.
Higher scores indicate better cognitive function.
Scores ≥26 are generally considered normal, with a 1-point adjustment for education ≤12 years; scores <26 suggest possible cognitive impairment.
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baseline
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The 39-Item Parkinson's Disease Questionnaire
Tijdsspanne: baseline
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Non-Motor Symptoms Scale (NMSS) assesses frequency and severity of non-motor symptoms across all stages of Parkinson's disease, covering autonomic, affective, cognitive, sleep, and other domains.
Total scores range from 0 to 360.
Higher scores indicate worse outcome (greater symptom burden).
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baseline
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Hamilton Depression Rating Scale
Tijdsspanne: baseline
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Hamilton Depression Rating Scale (HAM-D) is a clinician-rated instrument assessing depression severity across multiple dimensions including mood, somatic symptoms, anxiety, and sleep disturbance.
The 17-item version (HAM-D17) yields total scores ranging from 0 to 52.
Higher scores indicate worse outcome (greater depressive symptom severity), with scores ≥23 indicating very severe depression.
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baseline
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hoehn-yahr stage
Tijdsspanne: baseline
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Hoehn and Yahr Scale (HY) is a clinician-rated instrument assessing clinical severity and disease staging in Parkinson's disease.
Staging ranges from 0 (no symptoms) to 5 (severe disability requiring full dependence).
Higher stages indicate worse outcome (more advanced disease with greater functional impairment), primarily based on postural instability and disability.
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baseline
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Movement Disorder Society-Sponsored Revision Of The Unified Parkinson's Disease Rating Scale
Tijdsspanne: baseline
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Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) is a comprehensive instrument assessing Parkinson's disease across four parts: non-motor symptoms, activities of daily living, motor symptoms, and complications.
Total scores range from 0 to 260 (Part I: 0-52, Part II: 0-52, Part III: 0-132, Part IV: 0-24).
Higher scores indicate worse outcome (greater impairment).
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baseline
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Wearable devices measure gait parameters
Tijdsspanne: baseline
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Wearable Device System (GYENNO MATRIX) is a 10-sensor system sampling at 100 Hz to capture 3D angular velocity, acceleration, and geomagnetic field data.
It extracts gait parameters (step length, stride, gait cycle) and detects postural transitions (standing, sitting, turning).
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baseline
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Sniffin' Sticks 12
Tijdsspanne: baseline
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Sniffin' Sticks 12 (SS-12) is a brief olfactory screening test assessing odor identification ability using 12 pen-like odor pens.
Total scores range from 0 to 12, based on the number of correctly identified odors.
Higher scores indicate better outcome (superior olfactory function).
It is widely used for early Parkinson's disease screening and cognitive disorder assessment.
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baseline
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REM sleep behavior disorderscreening questionnaire
Tijdsspanne: baseline
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REM Sleep Behavior Disorder Screening Questionnaire (RBDSQ) is a 10-item self-rated scale screening for REM sleep behavior disorder, covering dream content, dream-enactment behaviors, injuries, and neurological conditions.
Total scores range from 0 to 13.
Higher scores indicate worse outcome (greater likelihood of abnormality), with scores ≥5 considered abnormal.
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baseline
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Parkinson's disease sleep scale
Tijdsspanne: baseline
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Parkinson's Disease Sleep Scale (PDSS) is a 15-item scale assessing sleep disturbances in Parkinson's disease, covering nighttime quality, sleep onset, maintenance, limb discomfort, dreaming, hallucinations, nocturia, and daytime sleepiness.
Total scores range from 0 to 150 (0-10 per item).
Higher scores indicate better outcome (fewer or less severe sleep problems).
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baseline
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 januari 2024
Primaire voltooiing (Geschat)
31 december 2027
Studie voltooiing (Geschat)
31 december 2027
Studieregistratiedata
Eerst ingediend
22 december 2025
Eerst ingediend dat voldeed aan de QC-criteria
25 juni 2026
Eerst geplaatst (Werkelijk)
1 juli 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
1 juli 2026
Laatste update ingediend die voldeed aan QC-criteria
25 juni 2026
Laatst geverifieerd
1 december 2025
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 2026KY647
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .