Skip to content

Assessing the effectiveness of Educational Package for Controlling Metabolic Syndrome Components

Design, Implementation and Evaluation of Lifestyle Modification Packages Based on Family Medicine Approach to Controlling Metabolic Syndrome Components

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200212046470N1
Enrollment
72
Registered
2020-02-23
Start date
2017-09-23
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

metabolic syndrome.

Interventions

Intervention group: received educational package consists of a three months’ schedul schedule ( First month: face- to- face and pamphlets education program .Second month: 14 educational message ,Thir

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: minimum age of 18 years old The inclusion criteria were as follows: existence of =3/5 elements for metabolic syndrome including: central obesity (men: =94 cm, women: =80 cm waist circumference); hypertension (systolic =130 mmHg, diastolic =85 mmHg and/or anti-hypertensive treatment); diabetes (fasting blood sugar (FBS) =100 mg/dL and/or anti-diabetic treatment); elevated triglycerides(TG) (=150 mg/dL); low high-density lipoprotein (HDL) (men: <40 mg/dL, women: <50 mg/dL) and/or cholesterol-lowering treatment

Exclusion criteria

Exclusion criteria: level of education less than fifth grade hepatic diseases, hematologic diseases, renal failure (GFR <30), Secondary causes of dyslipidemia, such as hypothyroidism and taking oral contraceptives, severe psychological illness, physical disability, known Cancer and treated type 1 diabetes, Alzheimer's and dementia Active TB disease, HIV

Design outcomes

Primary

MeasureTime frame
Anthropometric indices, blood pressure, lipid profiles, and fasting blood glucose. Timepoint: before intervention and after 3 month of intervention. Method of measurement: clinical Anthropometric measurement- Laboratory measurement- Clinical mercury manometer.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactshahed samat

Tehran University of Medical Sciences

sdrmed1@yahoo.com+98 21 8802 9686

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026