The Dampness Syndrome of Chinese Medicine Cohort Study

Cancer Clinical Trial

— DACOS  

Official title:

A Multi-Center Prospective Cohort Study of Dampness Syndrome in China

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05315895
• Other study ID #: SZ2021ZZ06
• Status: Recruiting
• Start date: June 6, 2022
• Est. completion date: March 30, 2028

Study information

• Verified date: November 2022
• Source: Guangzhou University of Traditional Chinese Medicine
• Contact: Jianwen Guo, MD
• Phone: +86-13724899379
• Email: 1308251832[@]qq.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The researchers plain to build a large-scale, longitudinal, prospective cohort characterized by TCM dampness syndrome. With the biobank of this cohort the investigators want to find the causality between TCM dampness syndrome and clinical chronic diseases and a new way to treat clinical disease.

Description:

DACOS is a national large- scale, longitudinal, multi-center, prospective, cohort study of natural person aged 35 to 75. The baseline survey and the follow-up surveys will be conducted in 5 areas covering the eastern, northern, western, southern and middle parts of China. In this study 100,000 natural person will be regularly followed up for 5 years(visited once a year), with the loss rate ≤15%. Three parts will be carried in the form of interview, physical examination and biological sample collection. During the interview, the investigators plan to do some questionnaires to learn participants' demographic characteristics, life style, disease history, healthy condition(EQ-5D-5L, SDS,), cognition state(AD-8, MMSE, MoCA) and the results of TCM syndrome differentiation(Score of Dampness syndrome and TCM constitution scale). All biological specimens (including blood, feces, urine, saliva and tongue coating) will be collected and stored in the biological resource center until researchers request their use. With the building up of this cohort, the researchers will analyze the causality between dampness syndrome and specific chronic diseases such as diabetes, coronary heart disease, cancer, dementia and so on.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100000
• Est. completion date: March 30, 2028
• Est. primary completion date: December 30, 2027
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 35 Years to 79 Years

Eligibility

Inclusion Criteria:

1. Residents aged 30 to 79, whose residence is consistent with their registered permanent residence location;

2. Residents who voluntarily participate in the project, agree to the collection of their biological information, and sign the informed consent form;

3. Residents who have no mental illness and other related diseases, and display a normal ability of expression and understanding;

Exclusion Criteria:

1. Residents who reject collaboration;

2. Residents who allow no follow-up visits.

Related Conditions & MeSH terms

• Aging
• Alzheimer Disease
• Alzheimer Disease, Early Onset
• Cancer
• Chronic Disease
• Dementia Alzheimers
• Metabolic Disease
• Metabolic Diseases

Intervention

Other:
• natural aging process
To observe the relationship between new cases of diseases and health status of people exposed to different factors such as life style, alcohol consumption, eating habits, etc.

Locations

Country	Name	City	State
China	Guangdong Province Hospital of Tradtional Chinese Medicine	Guangzhou	Guangdong

Sponsors (2)

Lead Sponsor	Collaborator
Guangzhou University of Traditional Chinese Medicine	State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	emerging diseases	This study will pay attention to the emerging situation of clinical chronic diseases, such as cancer, diabetes, hypertension, coronary heart disease, dementia, etc. Each follow-up the researchers will record the incidence of the emerging diseases of interviewees' by questionnaire including the name of the disease, time of onset and treatments.	through study completion, an average of 1 year
Secondary	Montreal Cognitive Assessment(MoCA)	MoCA is a brief, 30-question test that helps healthcare professionals detect cognitive impairments very early on, allowing for faster diagnosis and patient care. MoCA is the most sensitive test available for detecting Alzheimer's disease, measuring executive functions and multiple cognitive domains. The value range 0-30: higher scores mean a better Cognitine. The score above 26 is considered the normal congnitive level	through study completion, an average of 1 year
Secondary	European Quality of Life 5-dimensional questionnaire (EQ-5D-5L)	The EQ-5D comprises five dimensions of health: mobility, ability to self-care, ability to undertake usual activities, pain and discomfort, and anxiety and depression. . EQ-5D-5L, includes five levels of severity for each dimension (no problems, slight problems, moderate problems, severe problems, and extreme problems). The value range 0-100: higher scores mean a worse outcome.	through study completion, an average of 1 year
Secondary	Mini-Mental State Exam (MMSE)	MMSE is a widely used test of cognitive function among the elderly; it includes tests of orientation, attention, memory, language and visual-spatial skills. The value range 0-30: higher scores mean a better Cognitine.	through study completion, an average of 1 year
Secondary	interview questionnaire	Demographic characteristic, life style. disease history, allergies will be involoved.	through study completion, an average of 1 year
Secondary	change of the blood routine results	WBC, RBC, PLT , HB, NEUT% and LYM% will be tested and recorded. Above or below each mormal value will be considered as abnormal.	through study completion, an average of 1 year
Secondary	urine routine	urinary WBC and urinary RBC will be observed. negative or below 5/HP is normal.; BLO and GLU and PRO in urine will also be test. Negative is normal.	through study completion, an average of 1 year
Secondary	change of faeces routine	cells in faeces will be tested such as RBC and WBC. Negative occult blood(FOB) is difined normal.	through study completion, an average of 1 year
Secondary	change of hepatic function	The researchers will check the results of ALT and AST. TBil, DBIL, TBA and TP, ALB. Any indices above or below the criteria range is defined as abnormal. Every time point investigators will record the change of these indices.	an average of 1 year
Secondary	change of renal function	The researchers will check the results of Cr, BUN, TC, LDL, HDL,UA and fasting blood glucose,glycosylanted. Any indices above or below the criteria range is defined as abnormal. Every time point investigators will record the change of these indices.	an average of 1 year
Secondary	change of CRP	change of CPP	an average of 1 year
Secondary	change of Hcy	change of Hcy	an average of 1 year
Secondary	change of thyroid function	change of TSH ,FT3, FT4	an average of 1 year
Secondary	change of Vit B12 and folic acid	change of Vit B12	an average of 1 year
Secondary	change of coagulation function	change of PT, INR,TT,APTT,FIB	an average of 1 year
Secondary	change of abdominal ultrasound	change of abdominal ultrasound	an average of 1 year
Secondary	change of gynecologic ultrasound	change of gynecologic ultrasound	an average of 1 year
Secondary	change of ECG	The researchers will check the change of P, QRS and ST segments separately in electrocardiogram.	an average of 1 year
Secondary	change of brain MRI	change of brain MRI. The investigators will focus on the change of hippocampal volume and the spacing of temporal sulcus gyrus.	an average of 1 year