Risk factors of Non-communicable diseases.
Conditions
Interventions
Intervention 1: Group IV: Assessment of the main NCDs’ risk factors and setting time-bound targets, AND Finding and sharing evidence on effective/efficient interventions for controlling the risk facto
Sponsors
National Institute for Medical Research Development (NIMAD)
Eligibility
Sex/Gender
All
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: In the first study, three medical universities will be selected randomly from three different climates, and they will be asked to submit a list of health and medical and health centers in their urban and rural areas, broken down by health centers and health homes. Then the list of networks that have the entry criteria (descriptions in the entry criteria) are prepared and then the selection is made randomly. From each University, four Urban health centers and four health home randomly selected . Four groups (each consisting of a health center and a health center) will be introduced.Of course, to control the likelihood of data contamination, one of the universities(?Semnan), in addition to the intervention cluster city, will select another city(Garmsar) with 4 urban clusters and 4 rural clusters, which will receive no intervention. Universities eligible for entry into the study: 1. Have the consent to cooperate in the study. Cities eligible for entry into the study are: 1. Cities with at least four urban health centers and four health-care homes. Eligible entry centers: 1. Health homes with at least two "Behvarz". 2. City bases Have at least 2 health care staff. And preferably have recruiting staff . 3. health homes that are preferable to the Very small village .eligible staff : Preferably, have fixed forces (recruitment) of health centers and health homes At least 2 years into that center.
Exclusion criteria
Exclusion criteria: Disagreement with the text of the memorandum, by the relevant authorities of the universities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Population level of uncontrolled hypertension. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey.;Population level of Poorly controlled diabetes. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey.;Population level of insufficient physical activity. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey.;Population level of current tobacco smoking. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey.;Population level of insufficient intake of fruits/vegetables. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey.;Population level of body mass index. Timepoint: At the beginning of intervention (Month 0), 12 months after starting of intervention, 24 month after starting of intervention. Method of measurement: Population Survey. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaziar Moradi-Lakeh
Preventive Medicine and Public Health Research Center
Outcome results
None listed