hypertension
Conditions
Interventions
intervention group:a package of salt-reduction interventions
Control group:General life style in the study period, and will be given experimental protocol after one year intervention
Sponsors
Office of Non-communicable Disease Control and Community Health
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: (1) Selection of communities: A County/District is selected from each province. Ten communities are selected from each County/District. For the selection of communities, we will take into consideration of geographical area, urbanization, number of populations, structure of populations, economic status, health service resources, etc to ensure all the communities with similar characteristics. Communities in intervention group should be matched on every factor with those in control group. In each county, 6 rural communities and 4 urban communities will be selected; while in each district, 4 rural communities and 6 urban communities will be selected. The selected communities should have local workers to carry out the intervention activities from primary health service and supported by Neighborhood Committee (Women's federation worker). The community involved in other salt-reduction projects should be excluded. (2) Selection of evaluation samples: Individuals for evaluation will be randomly selected according to age, sex, education experience, command of health knowledge, health status, etc. Inclusion criteria for participants includes: (1) Aged 18-75 years old; (2) Two family members of each family are included; one of them is the major cook, and the other is selected by the order of couple, other adult family member (adult with opposite gender); (3) Both eat home-made meals at least 10 meals per week; (4) At least one selected member owns and can use smartphone; (5) Local residents for over 6 months, no out of community moving plan within 12 months; (6) Agree to sign informed consent form.
Exclusion criteria
Exclusion criteria: (1) Women in pregnant or lactation period; (2) Currently participate in any other clinical trial; (3) Individuals who cannot or refuse to collect 24-hour urine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 24 hour urinary sodium; | — |
Secondary
| Measure | Time frame |
|---|---|
| blood pressure;salt related knowledge-attitude-practice; | — |
Countries
China
Contacts
Public ContactJixiang Ma
Office of Non-communicable Disease Control and Community Health
Outcome results
None listed