ifestyle modification for Prevention of non-communicable disorders: Intervention phase of the Tehran Lipid and Glucose Study (phase II)
Not Applicable
Recruiting
- Conditions
- ifestyle modification interventions in preventing or postponing the development of NCD risk factors and outcomes with special focus on angina pectoris, myocardial infarction, cerebrovascular events, diabetes mellitus, hypertension and dyslipidemia..
- Registration Number
- IRCT138705301058N1
- Lead Sponsor
- research institute for endocrine sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 15005
Inclusion Criteria
Individuals aged 3 years and over who were residence of the District 13 of Tehran and were under the coverage of three medical health centers of Salavati, Mohammadian, and Lailatolghadr, were selected using multistage cluster random sampling method. All members of each family not mentally disabled, including those having or not having risk factors, were interviewed.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Major NCD risk factors including glucose disorders, dyslipidemia, obesity, smoking, HTN, level of physical activity, nutritional status. Timepoint: every 3 years. Method of measurement: The participants are interviewed by trained physicians to obtain past medical history and to complete a 110-item questionnaires regarding familial history of NCD, smoking habits, reproductive history and assessment of physical activity; brief physical examination is performed including anthropometric measurements. Rose angina questionnaire is completed and ECG is taken from individuals over 30 years of age. Trained dietitians collect dietary data in one tenth of the participated family.
- Secondary Outcome Measures
Name Time Method Any medical event with special focus on cardiovascular events. Timepoint: one year. Method of measurement: Every participant of the TLGS is followed up for any medical event during prior year by telephone call. He/she is asked for any medical conditions by a trained nurse and if a related event had occurred a trained physician collects complementary data during a home visit. If necessary, she pays a visit to respected hospital and collects data from medical files. In the case of mortality, data are collected from hospital or death certificate by local physician.The collected data were then evaluated by an outcome committee to assign a specific outcome for every event.