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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03649503
Other study ID # KY2016-214
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2018
Est. completion date September 30, 2033

Study information

Verified date September 2023
Source Huashan Hospital
Contact Jian Wang, MD
Phone 86-21-52888160
Email wangjian336@hotmail.com, Wangjian_hs@fudan.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The overall goal of this project is to identify, assess and longitudinally monitor subjects who are interested in participating in this study. Participants will enroll through a platform named PaWei, and provide informed consent prior to any study activities. PaWei will collect a variety of information, including participants' demographic information, overall health, family history of Parkinson's Disease, other clinical information (clinical drug use, drug efficacy, and comorbid disorders), mood status, sleep, diet, exercise, memory complaints, online cognitive tests, the Short-Form 8-Item Parkinson's Disease Questionnaire (PDQ-8), Movement Disorder Society-Unified Parkinson's Disease Rating Scale IB & II (MDS-UPDRS IB & II), Non-Motor Symptom Aassessment Scale for Parkinson's Disease (NMSS) , Hoehn and Yahr Scale, and other scales related to quality of life, etal---all through self-reported online questionnaires. Participants will also be asked to return to the PaWei every 3 months at regular intervals, to complete follow-up scales related to quality of life, and neuropsychological assessments, etal. Anyone with Parkinsonian Disorders is welcome to participate.


Description:

In April 2017, the investigators launched a platform named PaWei which contains an iOS and Android smartphone application for patients and doctors. The platform connects patients, doctors and researchers by establishing communication and data transfer between the cloud platform and the mobile applications over the internet. The PaWei app is made available for free to download through the Apple App Store and Android Market. Through national outpatient service, advertisement and community outreach, potential participants will be directed to the PaWei APP. The overall goal of this project is to identify, assess and longitudinally monitor subjects who are interested in participating in this study. Participants will enroll through the PaWei APP, and provide informed consent prior to any study activities. The PaWei APP will include: 1. Information about the National Registry Study (who is eligible to participate, the goals of the project and other relevant information about investigators and sponsors involved in the Initiative). 2. Frequently Asked Questions (FAQs) such as "How will my information be used?", "How will patient information be safeguarded?", "What information will be requested?", "How much time will be required for registration and testing?" will be addressed for participants. 3. General information about Parkinsonian Disorders. The National Registry Study will be a large, online database of volunteers who are interested in participating in this study. Anyone with Parkinsonian Disorders is welcome to join the Registry. 1. Participants will provide their email address or telephone number and create an account and username with the Registry. 2. The Registry will send an automatic email or short message to the participant to verify their email address or telephone number. 3. Participants will read the online Information Sheet and will be asked to provide their consent by clicking either "I consent" or "I decline." Participants who decline to participate in the Registry will be not included in our study. 4. Participants who give their consent will be permitted to continue through the registration process, which includes completing a battery of questionnaires designed to obtain a general understanding of participants health, medical history wellbeing. 5. In addition to questionnaires, participants will be able to complete online scales related to quality of life, and cognitive assessments. 6. Participants will be given the option to elect a Caregiver and/or Study Partner (CASP) to enrich their study profile. 7. Video recordings: Participants are asked to perform finger tapping, hand movements, and walking in MDS-UPDRS III test after being instructed by the video example, and then to upload the videos to the PaWei APP. The severity of motor dysfunctions on those videos can be judged by clinicians, and be potentially quantified in the future by AI technology under development. 8. Data validation: (1) The quality control of raw data is the initial step of data analysis for any successful research. In PaWei platform, the investigators take a strategy of assessing the data quality by identifying poor-quality data, like incomplete data and illogical data based on the logistic verification about consistency of relevant questions. (2) Automated feedback loops are employed with this strategy to enable real-time detection of incomplete data or illogical data, which can be used to improve data collection quality. 9. Participants may be referred to other research studies and/or clinical trials.


Recruitment information / eligibility

Status Recruiting
Enrollment 100000
Est. completion date September 30, 2033
Est. primary completion date September 30, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Anyone with Parkinsonian Disorders is welcome to join the Registry. Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention


Locations

Country Name City State
China Huashan Hospital Shanghai Shanghai
China Huashan Hospital Affiliated to Fudan University Shanghai Shanghai

Sponsors (55)

Lead Sponsor Collaborator
Huashan Hospital Af?liated Hospital of North Sichuan Medical College, Affiliated Hospital of Guangdong Medical University, Affiliated Hospital of Jiangsu University, Anhui Provincial Hospital, Changshu Hospital of Traditional Chinese Medicine, China-Japan Union Hospital, Jilin University, Chinese PLA General Hospital, Daqing Oil Field Hospital, First Affiliated Hospital of Chongqing Medical University, First Affiliated Hospital of Harbin Medical University, First Affiliated Hospital, Sun Yat-Sen University, Fujian Medical University Union Hospital, Fujian Provincial Hospital, Gansu Provincial Hospital, Guangxi Ruikang Hospital, Huadong Hospital, Jieyang People's Hospital, Jingjiang People's Hospital, Lianyungang Hospital Affiliated Bengbu Medical College, Luoyang Central Hospital, Ningbo No. 1 Hospital, No. 102 Hospital of Chinese People's Liberation Army, Northern Jiangsu Province People's Hospital, Peking Union Medical College Hospital, Qingdao Municipal Hospital, Second Affiliated Hospital of Nanchang University, Shandong Provincial Hospital, Shanghai 10th People's Hospital, Shanghai 5th People's Hospital, Shanghai Changzheng Hospital, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai Zhongshan Hospital, Suzhou Municipal Hospital, Taian City Central Hospital, Taizhou Hospital, The 101st Hospital of Chinese People's Liberation Army, The Affiliated Hospital of Qingdao University, The Affiliated Hospital of Xuzhou Medical University, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, The First Affiliated Hospital of Dalian Medical University, The First Affiliated Hospital of the Fourth Military Medical University, The First Affiliated Hospital of Zhengzhou University, The First Affiliated Hospital with Nanjing Medical University, The First Hospital of Hebei Medical University, The First People's Hospital of Changzhou, The First People's Hospital of Jingzhou, The Second Affiliated Hospital of Harbin Medical University, Third People's Hospital, Huzhou City, Zhejiang Province, China, Tianjin Medical University General Hospital, Wuhan No.1 Hospital, Xi'an Central Hospital, Xi'an No.3 Hospital, Zhejiang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in the Short-Form 8-Item Parkinson's Disease Questionnaire (PDQ-8) Score The short-form 8-item Parkinson's disease Questionnaire (PDQ-8) is the most commonly used scale measuring health related quality of life (HRQoL) in PD patients. It includes 8 items, and each item has five options (never, occasionally, sometimes, often, always or cannot do at all). The total scores range from 0 (good health) to 32 (poor health). The change of PDQ-8 score is defined as the score collected at visit 4 (end of year 1), visit 8 (end of year 2), visit 12 (end of year 3), visit 16 (end of year 4), visit 20 (end of year 5), visit 24 (end of year 6), visit 28 (end of year 7), visit 32 (end of year 8), visit 36 (end of year 9), visit 40 (end of year 10), and final visit (last study visit or early withdrawal visit, up to 10 years) minus baseline score.
Analysis Method: Mixed Model Repeated Measures (MMRM)
Baseline, year 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, and final visit (last study visit or early withdrawal visit, up to 10 years)
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