Home Blood Pressure Monitoring Registration Study in the Elderly(HOME Study)
Home Blood Pressure Registration Study on Community Elderly Population(HOME Study)
1 other identifier
observational
6,000
1 country
2
Brief Summary
China is entering an aging society. As the number of elderly population continues to increase, the elderly are facing many social problems that deserve the attention of all sectors of society. Hypertension is one of the common diseases in the elderly population. Hypertension is the most common chronic diseases and a most important risk factor for cardiovascular and cerebrovascular diseases, and also a substantial public health problem. Home blood pressure monitoring is simple, not only can find hypertension, but also can guide the treatment of patients with hypertension. The purpose of the study is to investigate the association between home blood pressure and adverse outcomes in community elderly population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2020
Longer than P75 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 24, 2019
CompletedFirst Posted
Study publicly available on registry
December 27, 2019
CompletedStudy Start
First participant enrolled
January 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2050
ExpectedJanuary 13, 2020
December 1, 2019
5 years
December 24, 2019
January 10, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
All-Cause Mortality
All-cause mortality was confirmed through a combination of hospital medical records, telephone contacts with patients or family members, and death registration at the Center for Disease Control and Prevention.
From date of inclusion until the date of death from any cause, assessed up to 1 year
Cardiovascular Mortality
Cardiovascular mortality was defined as death attributable to an ischemic cardiovascular cause (including fatal cardiovascular events and stroke).
From date of inclusion until the date of death from any cause, assessed up to 1 year
Secondary Outcomes (5)
Secondary outcomes of cardiovascular diseases
Through study completion, an average of 1 years
Secondary outcomes of cerebrovascular diseases
Through study completion, an average of 1 years
Secondary outcomes of kidney
Through study completion, an average of 1 years
Secondary outcomes of hypertension
Through study completion, an average of 1 years
Secondary outcomes of diabetes
Through study completion, an average of 1 years
Other Outcomes (1)
Number of participants with reported hospitalization due to other diseases
From date of inclusion until the date of first event, assessed up to 1 year
Interventions
no intervention
Eligibility Criteria
Study population includes subjects who living in community, of any race or ethnicity, 65 or older years of age.
You may qualify if:
- ≥65 years old
- Signed informed consent
- Life expectancy is greater than 1 year
You may not qualify if:
- \<65 years old
- Unsigned informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Feng Yingqing
Guangzhou, Guangdong, 510080, China
Guangdong Provincial People's Hospital
Guangzhou, Guangdong, 510080, China
Biospecimen
This study will collect 20 mL whole blood samples from subjects at one or more study visits. The whole blood will be processed to plasma and stored for testing.
Study Officials
- STUDY CHAIR
Feng Ying-qing, PhD
Guangdong Provincial People's Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 30 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 24, 2019
First Posted
December 27, 2019
Study Start
January 1, 2020
Primary Completion
December 31, 2024
Study Completion (Estimated)
December 31, 2050
Last Updated
January 13, 2020
Record last verified: 2019-12
Data Sharing
- IPD Sharing
- Will not share