nulliparous. XXI
Conditions
Interventions
Intervention 1: Recognize randomized trial using focus groups to prepare for the needs assessment of educational content and implementation of three training classes for groups. Intervention 2: Random
Lifestyle
Recognize randomized trial using focus groups to prepare for the needs assessment of educational content and implementation of three training classes for groups
Randomized trial and then two months later recognize pre-test and post-test in the control group.
Sponsors
Research Department, Shahid Sadoughi Yazd University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 35 Years
Inclusion criteria
Inclusion criteria: The conditions of entry into the study: the first pregnant women who had a live child from 1 day to 1 year old; not have abortions; the history of cardiovascular disease, gynocologic diseases, psychologic diseases, diabetes mellitus, hypertension, drug consumption due to medical problems; age between 15-35 years old; ability at least to read and write; 6. living in the Noshahr city, Iran. Exclusion criteria of the study: nulliparous women refused to continue participating in the study; nulliparous women who leave Noshahr city; nulliparous women with new obstetrics or other medical problems.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The quality of life. Timepoint: Before and two months after the intervention. Method of measurement: World Health Organization Quality of Life Inventory shortened standard. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNeda Ghazinezhad
Shahid Sadoughi Yazd University of Medical Sciences
Outcome results
None listed