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Lifestyle modification for Prevention of non-communicable disorders: Intervention phase of the Tehran Lipid and Glucose Study (phase II)

Prevention of non-communicable disease in a population in nutrition transition: Tehran Lipid and Glucose Study (Phase II)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138705301058N1
Enrollment
15005
Registered
2008-10-29
Start date
1998-12-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lifestyle 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..

Interventions

Control group: routine health care
Intervention 1: Intervention group: Primary, secondary and tertiary interventions were designed based on specific target groups including schoolchildren, housewives, and high-risk persons. Officials o
Intervention group: Primary, secondary and tertiary interventions were designed based on specific target groups including schoolchildren, housewives, and high-risk persons. Officials of various sector

Sponsors

research institute for endocrine sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 99 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. A.A. Momenan

TLGS unit

momenan@endocrine.ac.ir+98 21 7746 2216

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 3, 2026