Comparison the effectiveness of lifestyle modification interventions

Phase 2

• Conditions: ife-style (Factors influencing health status and contact with health services).; Persons encountering health services for specific procedures and health care; Z40,Z41,Z4

• Registration Number: IRCT2015070423055N1
• Lead Sponsor: Vice Chancellor for research of Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Inclusion Criteria: Age 40-60 years; Living in Amirkola Babol; Desire to participate in the study, fill out and sign the informed consent form of the research

Exclusion Criteria

Unable to read and write; Pregnancy or child breast feeding; Severe physical or mental disease which make them disable; Probable migration from Amirkola in 10 months

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ife style status. Timepoint: Before ( 0 week) and after the intervention (16th week). Method of measurement: HPLP-II questionnaire (Health-Promoting Life Style Profile-II).;Main dietary pattern. Timepoint: Before ( 0 week) and after the intervention (16th week). Method of measurement: Food Recall Questionnaire.;Physical activity status. Timepoint: Before ( 0 week) and after the intervention (16th week). Method of measurement: IPAQ:International Physical Activity Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Anthropometric measures. Timepoint: Before (0 week) and after the intervention (16 th week). Method of measurement: Physical examination.;Blood pressure. Timepoint: Before (0 week) and after the intervention (16 th week). Method of measurement: Physical examination.;Fasting blood glucose. Timepoint: Before ( 0 week) and after the intervention (16 th week). Method of measurement: Blood sample.;Serum lipid profile. Timepoint: Before ( 0 week) and after the intervention (16 th week). Method of measurement: Blood sample.