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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	ClinicalTrials.gov
Last refreshed on:	16 December 2017
Main ID:	NCT02368418
Date of registration:	02/09/2014
Prospective Registration:	No
Primary sponsor:	The George Institute for Global Health, China
Public title:	China Rural Health Initiative Follow up Study CRHIFU
Scientific title:	China Rural Health Initiative Follow up Study
Date of first enrolment:	September 2014
Target sample size:	9164
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT02368418
Study type:	Observational
Study design:
Phase:	N/A

Countries of recruitment
China

Contacts

Name:	Yangfeng Wu, PhD
Address:
Telephone:
Email:
Affiliation:	The George Institute for Global Health, China

Key inclusion & exclusion criteria

Inclusion Criteria:

- Individuals had participated the baseline or post-intervention survey.

Exclusion Criteria:

- Death

Age minimum: 50 Years
Age maximum: N/A
Gender: All

Health Condition(s) or Problem(s) studied

Cardiovascular Disease

Intervention(s)

Procedure: PCP

Procedure: SRS

Primary Outcome(s)

mean systolic blood pressure level among all participants and those at high risk [Time Frame: from baseline and post-intervention to the follow up]

Secondary Outcome(s)

Proportion of individuals receiving lifestyle advice among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals regularly visiting the village clinic among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals using low sodium salt among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals adopting healthy behavior among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals developing CVD event among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals having knowledge on salt reduction among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals treated with a blood pressure lowering agent among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Proportion of individuals treated with aspirin among all participants and high-risk patients [Time Frame: from baseline and post-intervention to the follow up]

Secondary ID(s)

PKU00001052

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:
Date Posted:
Date Completed:
URL:

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