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IRCT20170927036445N2 IRCT 2018-03-10 Esfahan University of Medical Sciences post partum cares educational program for women with preeclampsia A study of a post partum cares educational interventional program for women with preeclampsia 2018-02-19 anticipated 60 Complete https://irct.ir/trial/29464 interventional Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Other design features: Random assignment is provided to intervention and control groups with the help of random numbers and one day, Randomization description: Simple randomization. N/A preeclampsia. Intervention 1: Intervention group: In intervention group, an interventional educational program designed for women with preeclampsia history. Intervention 2: Control group: the usual care was taken for the control group. Undecided - It is not yet known if there will be a plan to make this available Justification or reason for indecision in sharing IPD is No more information
public Mastaneh Kamravamanesh
Isfahan University of Medical Sciences, Faculty of Nursing Midwifery, Department of Ph.D. Students, Mastaneh Kamravamanesh
Isfahan Iran (Islamic Republic of) 81746-73461 +98 31 3668 7153 m_kamravamanesh@kums.ac.ir Esfahan University of Medical Sciences scientific Ziba Farajzadegan
Isfahan University of Medical Sciences - preventive Medicine Group
Isfahan Iran (Islamic Republic of) 73461-81746 +98 31 3668 0042 farajzadegan@mui.med.ac.ir Esfahan University of Medical Sciences Iran (Islamic Republic of) Inclusion criteria are women aged between 15-49 years, Iranian nationality, consent to participate in the study, ability to understand questions or ability to read and write, not participating in any other clinical trials at the same time, no severe mental disorders that requires to be under medical treatment or hospitalization, the nulliparous women with preeclampsia whose delivery resulted in live births. 15 years 49 years Female The exclusion criterion is not completing the intervention for any reason and being under treatment due to sever complication of preeclampsia, severe life stress , the death of the spouse or immigration and so on . Pre-eclamp 014 Lifestyle N/A Intervention group: In intervention group, an interventional educational program designed for women with preeclampsia history. Control group: the usual care was taken for the control group. Life style. Timepoint: Before intervention, 1 month later, 3 months after intervention. Method of measurement: life style questionnaire. Esfahan University of Medical Sciences Approved 2016-08-27 کمیته اخلاق دانشگاه علوم پزشکی اصفهان Hezar jarib Ave,Isfahan, Isfahan University of Medical Sciences, Isfahan Isfehan Iran (Islamic Republic of)