MedPath

The effect of preconception counseling on women lifestyle

Phase 2
Conditions
ifestyle.
Lifestyle-related condition
Registration Number
IRCT2016012610324N28
Lead Sponsor
Vice chancellor for research, Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
152
Inclusion Criteria

Non pregnant women ages 18-35 years old; Having secondary school and higher education level; Having ability to becoming pregnant (no history of hysterectomy, tubectomy and other reasons of infertility); Having plan to become pregnant in the next one year; Having health record in health center; Being interested in participating in the study; Having a contact number for follow-up.
Exclusion criteria: Having any diseases including cardio-vascular, hypertension, diabetes and mental diseases according to the woman expression.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Preconception lifestyle. Timepoint: Before, 4 and 8 week after intervention. Method of measurement: Preconception lifestyle questionnaire.
Secondary Outcome Measures
NameTimeMethod
Perceived Stress. Timepoint: Before, 4 and 8 week after intervention. Method of measurement: Perceived Stress Scale (PSS).;Preconception lifestyle knowledge. Timepoint: Before, 4 and 8 week after intervention. Method of measurement: Preconception lifestyle knowledge questionnaire.;Locus of control. Timepoint: Before, 4 and 8 week after intervention. Method of measurement: Multidimensional health locus of control scale B (MHLC).
© Copyright 2025. All Rights Reserved by MedPath