The effect of lifestyle based educational package on physical activity and nutritional status in obese and overweight pregnant wome

Phase 2

• Conditions: Lifestyle-related condition; Obesity.

• Registration Number: IRCT2016041210324N31
• Lead Sponsor: Vice chancellor for research, Tabriz 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: Female
• Target Recruitment: 140

Inclusion Criteria

Pregnant women with gestational age of 16-20 weeks; Having evidence regarding singleton and non-problematic pregnancy; Women with first, second and third pregnancy; Having health record in health center; Having at least secondary school education; Body mass index higher than 25 in preconception care or first trimester of pregnancy; Not participation in other similar studies; Being interested in participating in the study; Women ages 18 years old and higher.
Exclusion criteria: Having any diagnosed mental and physical diseases in mother; Following of special diet (according to mother’s expression); Having hospitalization history at present pregnancy; Change of living place during study implementation; Separation from husband; Addiction or habitual use of alcohol or addictive drugs; Having infertility history and using of assisted reproductive technologies; Having history of relatives death, divorce and acute emotional problems in the last month.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Physical activity score. Timepoint: 4 and 8 weeks after intervention. Method of measurement: International Physical Activity Questionnaire (IPAQ).;Food subgroups score. Timepoint: 4 and 8 weeks after intervention. Method of measurement: Food Frequency Questionnaire (FFQ).

Secondary Outcome Measures

Name	Time	Method
Weight gain rate. Timepoint: 8 weeks after intervention. Method of measurement: Scale (Model: Seca, Germany).;Frequency of gestational diabetes. Timepoint: 8 weeks after intervention. Method of measurement: Two-hour Oral Glucose Tolerance Test (OGTT) in 26 to 30 weeks.