gestational diabetes. Diabetes mellitus arising in pregnancy
Conditions
Interventions
Intervention 1: patients in the control group received routine prenatal visits by Diabetologist and obstetrician or midwife and only education based on the theory of planned behavior did not receive
Behavior
patients in the control group received routine prenatal visits by Diabetologist and obstetrician or midwife and only education based on the theory of planned behavior did not receive So that was men
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: (1) Written informed consent have for participation in the study (2) Maternal gestational age 20-24 weeks at the time of study entrance based on The first day of the last menstrual or the first half of pregnancy ultrasoundS (3) Iranian and resident of Mashhad (4) At least fifth grade literacy (5) Pregnant women with diagnosis of gestational diabetes are treated with human insulin (not analog) (6) Being able to communicate verbally.(7).No alcohol, smoking and drugs (8) dose not medical history of the medical disease (9).dose not referral to the psychiatrist or psychologist During the year prior and medication and hospitalization due to mental illness (10) dose not a high risk pregnancy (11) dose not to the cause underlying disease taking Continuously Glucocorticoid therapy (12) have The phone number for contact. Exclusion criteria during the study: (1) lack of willingness to continue participation in study (2) major stressful events during the study (3) the absence in any training sessions (4) The occurrence of pregnancy-related complications.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self Care Behavior. Timepoint: Baseline (pre-intervention) and one month after intervention. Method of measurement: questionnaire.;Self care Behavior. Timepoint: Baseline (pre-intervention) and one month after intervention. Method of measurement: questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood glucose tests was including fasting blood glucose and Blood glucose two hours after a meal. Timepoint: before and four weeks after the completion of the intervention. Method of measurement: Blood tests.;Level Blood glucose. Timepoint: Baseline (pre-intervention) and one month after intervention. Method of measurement: Blood tests. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Hoseinzadeh
Mashhad University of Medical Sciences
Outcome results
None listed