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A Multicenter Cohort Study on Acupuncture Treatment for Parkinson's Disease utilizing an Intelligent Cohort Data Management Platform based on CDISC Standards

A Multicenter Cohort Study on Acupuncture Treatment for Parkinson's Disease utilizing an Intelligent Cohort Data Management Platform based on CDISC Standards

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025001841
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Parkinson's Disease

Interventions

Non-exposed group:Parkinson's Disease Medications
Exposure group:Parkinson's Disease Medications + Electroacupuncture

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1)Patients who meet the International Parkinson and Movement Disorder Society (MDS-PD) clinical diagnostic criteria for Parkinson's Disease (2015).2)Patients with constipation spontaneous sweating nocturia etc. that appeared or worsened after the onset of Parkinson's Disease-related symptoms.3)Age = 40 years and = 80 years no gender restrictions.4)Patients currently undergoing anti-Parkinson's disease conventional medication treatment with stable drug dosages for at least 2 weeks.5)Patients who voluntarily participate in this study and provide informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients with secondary Parkinson's Disease (including those caused by vascular inflammatory toxic drug-induced traumatic hydrocephalus or neoplastic factors) and patients with Parkinson-plus syndromes (including Multiple System Atrophy Progressive Supranuclear Palsy Corticobasal Degeneration Lewy Body Dementia etc.).2)Patients currently suffering from severe life-threatening diseases such as serious cardiovascular cerebrovascular or hematopoietic system diseases or malignant tumors.3)Patients with a past or current diagnosis of psychotic disorders such as schizophrenia or severe depression or those with severe cognitive dysfunction (Mini-Mental State Examination MMSE = 17 points).4)Patients who cannot undergo acupuncture treatment due to skin conditions or limb deformities in the acupoint areas selected for this study.5)Patients who have participated in or are currently participating in other clinical trials within 30 days (1 month) prior to enrollment.6)Patients who have taken antidepressant analgesic or antihistamine medications affecting PD symptoms within 3 weeks prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Unified Parkinson Disease Rating Scale;

Secondary

MeasureTime frame
Nocturia episodes over 7 days;Parkinson's Disease Sleep Scale - Revised;Time and Steps Required for a 20-Meter Walk;Self-Rating Anxiety Scale;Hyperhidrosis Disease Severity Scale;39-item Parkinson Disease Question;Adverse Event;Parkinson's Disease Symptom Elements Scale;Visual Analog Scale (VAS) for Sweating Severity;Bowel Movement Diary;Non-Motor Symptoms Scale for Parkinson's Disease;Mini-Mental State Examination;Self-rating depression scale;Chronic Constipation Severity Scale;Schwab and England Activities of Daily Living Scale;Revised Hoehn and Yahr Staging;Epworth Sleepiness Scale;sleep diary;Bristol Stool Form Scale;Parkinson's Disease Medication Usage;

Countries

China

Contacts

Public ContactZhaoqin Wang

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine

wangzhaoqin@fudan.edu.cn+8618621153795

Outcome results

None listed

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