Contraception, intrauterine devices (IUD). Insertion of (intrauterine) contraceptive device
Conditions
Interventions
Intervention 1: Intervention group: 5 sessions of individual motivational interview was done once a week. Intervention 2: Control group: received no intervention.
Lifestyle
Intervention group: 5 sessions of individual motivational interview was done once a week.
Control group: received no intervention.
Sponsors
Vice chancellor for research, Arak University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: the women of reproductive age (15 to 49 years old)? being able to read and write? the absence of contraindication of insertion of intrauterine devices (IUD) like pregnancy, puerperal sepsis, the risk of pelvic inflammatory diseases or sexually transmitted diseases at the present or in the past 3 months, endometrial or cervical cancer, undiagnosed genital bleeding, uterine malformations, fibroid tumors that changes uterine anatomy, allergy to copper, Wilson disease? women who were at high risk of pregnancy (smoking, women with less than 3 years interval between the present pregnancy and previous childbirth, addiction, malnutrition and age over 35 years old, women with more than 4 pregnancies and chronic disease that if pregnancy occurs ,it will endanger the person's health)? women who had all the above-mentioned criteria, decided to use a secure method of contraception, but because of myths, they were uncertain about choosing intrauterine devices (IUD). Exclusion criteria: participants unwillingness to continue consultation sessions? absence of more than two sessions.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Use of intrauterine devices like IUD. Timepoint: Before and one month after the end of intervention. Method of measurement: Awareness, attitude and operation research questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Awareness, attitude and operation. Timepoint: Before and one month after the end of intervention. Method of measurement: Awareness, attitude and operation research questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSajedeh Molavi
Arak University of Medical Sciences
Outcome results
None listed