Skip to content

Parkinson's Disease Registry

Parkinson's Disease Registry(PDR)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02051205
Enrollment
200
Registered
2014-01-31
Start date
2012-12-31
Completion date
2014-12-31
Last updated
2014-01-31

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

Conditions

Parkinson Disease

Keywords

Parkinson's disease, risk factors, epidemiology

Brief summary

The purpose of the Parkinson's disease Registry (PDR) is to develop a nation-wide database of persons with Parkinson's disease (PD) in Taiwan.

Detailed description

Among degenerative neurological disease, PD is the second most common disorder. Although a wide range of incidence and prevalence rate exist in reviewed literatures due to a consequence of variation in study methodologies, the crude prevalence rate above 60 year-old is 1%. Increase in aging population will lead to an increase in PD patients. The PDR will be used to facilitate the understanding of basic epidemiological features of the disease, genetic and non-genetic risk factors, co-morbidity, the up-to-date treatment strategies and the related economic burden from medical and surgical treatment (deep brain stimulation), to develop new therapeutic protocols as well as healthcare policies, and ultimately, to improve the quality of life of PD patients. PDR will also be served as data bank for investigators in the field of PD to quickly identify and notify research subjects about other research studies for which they are eligible. Patient who registered can also sign their consent for a future brain donation after they passed away. Methods: The 4 main Tzu Chi Hospitals from Hualien, Da Lin, Taichung, and Taipei will serve as representative of pilot study for National registry. This will be a record-based, multi-center, nation-wide, cohort study. A user-friendly, yet, encrypted registration platform will be provided through internet for authorized personnel. The contents of PDR will be as follow: demographic features, risk factors, clinical profiles of diagnostic criteria, co-morbidity, images profiles, treatment regimens in details, prognosis, health-related quality of life, and neuropsychological assessment batteries. Expected results: 1. To facilitate the understanding of demographic epidemiological features of PD. 2. To find the risk factors of PD and the possible intervention toward disease prevention in Taiwan. 3. To find the comorbidity of the disease, and the solution toward better treatment and related outcome. 4. Assess current treatment approaches and develop best-practice guidelines. 5. Tracking the health-related quality of life of PD patient as well as care-givers and the economic impact from different treatment regimens of best medications versus surgical interventions (neuromodulation / neuro-regeneration) from time to time. 6. Drive the development of innovative research projects. 7. Accelerate the process of informing patients of research projects for which they may be eligible. Key words: Parkinson's disease, Registry, Epidemiology, Treatment, Prognosis

Interventions

None listed

Sponsors

Buddhist Tzu Chi General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Parkinson's disease

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Risk factors1 yearrisk factors include: pesticide, herbicide, drinking underground water, jobs with heavy metals exposure, tea drinking, coffee drinking, smoking, vegetarian

Secondary

MeasureTime frameDescription
Motor function1 yearAssessment with Unified Parkinson's Disease Rating Scale (UPDRS) part 3. Rating when l-dopa medication On and Off, to see the improvement %.

Other

MeasureTime frameDescription
Depression1 yearAssessment with Beck's depression inventory (BDI) and UPDRS part 1.
Comorbidity1 yearHypertension, diabetes mellitus, stroke, cardiovascular disease, alcoholism, epilepsy, brain surgery, memory impairment, hallucination.
Cognitive function1 yearRating with Mini-mental status examination (MMSE) and Cognitive abilities screening instrument (CASI)
Initial PD symptoms1 yearTo identify the initial cardinal symptom: bradykinesia, tremor, rigidity and posture instability
Cost of medical treatment1 yearIdentify individual medications and represented as levo-dopar equivalent daily dose (LEDD)
Quality of life1 yearAssessment with Parkinson disease questionnaire (PDQ-39), UPDRS part 2, and Schwab and England activity of daily living (SEADL)

Countries

Taiwan

Contacts

Primary ContactTingwen Hou
tingwen.hou@msa.hinet.net+886-3-8561825

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026