NCT04212468

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
6,000

participants targeted

Target at P75+ for all trials

Timeline
299mo left

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

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

Study Progress21%
Jan 2020Dec 2050

First Submitted

Initial submission to the registry

December 24, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 27, 2019

Completed
5 days until next milestone

Study Start

First participant enrolled

January 1, 2020

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
26 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2050

Expected
Last Updated

January 13, 2020

Status Verified

December 1, 2019

Enrollment Period

5 years

First QC Date

December 24, 2019

Last Update Submit

January 10, 2020

Conditions

Keywords

Blood PressureElderly

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

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

NOT YET RECRUITING

Guangdong Provincial People's Hospital

Guangzhou, Guangdong, 510080, China

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

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

  • Feng Ying-qing, PhD

    Guangdong Provincial People's Hospital

    STUDY CHAIR

Central Study Contacts

Feng Ying-qing, PhD

CONTACT

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

Locations