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A Prospective Cohort Study Investigating Multimodal Biomarkers for Early Diagnosis, Differential Diagnosis, and Prognostic Prediction in Parkinson’s Disease and Parkinson-Plus Syndromes

A Prospective Cohort Study Investigating Multimodal Biomarkers for Early Diagnosis, Differential Diagnosis, and Prognostic Prediction in Parkinson’s Disease and Parkinson-Plus Syndromes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112049
Enrollment
Unknown
Registered
2025-11-10
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's disease and Parkinson-Plus Syndromes

Interventions

Parkinson-Plus Syndromes:None
Healthy control:None

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Participants should meet the following criteria: 1. Provide a signed and dated informed consent form; 2. Agree to comply with study procedures and participate in the entire research process; 3. Aged between 50 and 80 years; 4. Meet the diagnostic criteria and exhibit the characteristic symptoms and signs of specific diseases (e.g., PD, MSA, DLB, CBD, PSP), or be generally in good health; 5. Have adequate physical, cognitive, auditory, speech, literacy, and language abilities to complete all required assessments.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they meet any of the following criteria: 1. Presence of other neurological disorders such as cerebrovascular disease, traumatic brain injury, major systemic diseases (e.g., hepatic or pulmonary encephalopathy), or intracranial space-occupying lesions (e.g., subdural hematoma, brain tumor); 2. Evidence of significant structural brain abnormalities, including ischemic infarction, subdural hematoma, intracranial hemorrhage, hydrocephalus, brain tumor, multiple subcortical ischemic lesions, or a single lesion in critical regions (e.g., thalamus). Mild, clinically insignificant white matter changes or no more than two lacunar infarctions are acceptable; 3. Inability to undergo MRI scanning due to conditions such as claustrophobia or cardiac pacemaker implantation; 4. Psychiatric disorders diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) within the past 12 months that are unstable or could interfere with study assessments, including schizophrenia or other psychotic disorders, bipolar disorder, major depressive disorder, or delirium; 5. Diagnosis of alcohol or substance abuse or dependence within the past 12 months based on DSM-V criteria; 6. Poor compliance or inability to complete the study as judged by the investigators; 7. Inability to undergo MRI or PET imaging.

Design outcomes

Primary

MeasureTime frame
Biomarkers and digital biomarkers differentiating PD subtypes;

Secondary

MeasureTime frame
Biomarkers and digital biomarkers for differentiating PD from PDS;

Countries

China

Contacts

Public ContactChen Shengdi

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

chensd@rjh.com.cn+86 138 1801 8166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026