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The effect of implementation of the group educational-care model in pregnant women with diabetes

The effect of implementation of the centering pregnancy group prenatal educational-care model in pregnant women with diabetes: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120718010324N80
Enrollment
100
Registered
2024-01-03
Start date
2024-04-03
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

prenatal care. Supervision of other high-risk pregnancies

Interventions

Intervention 1: Intervention group: For individuals in the intervention group, in addition to routine prenatal care, an eight-week intervention will be provided in the form of group sessions held ever

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
10 Years to 54 Years

Inclusion criteria

Inclusion criteria: Women with gestational diabetes or type 2 diabetes Gestational age 24 to 28 weeks The possibility of the presence of participants (according to the place of residence) in group meetings before childbirth, for 8 weeks at specific places and times in the city of Tabriz.

Exclusion criteria

Exclusion criteria: Multiple pregnancy Major fetal anomalies The presence of medical diseases The presence of psychiatric diseases Suffering from advanced and complicated diabetes (nephropathy, retinopathy and neuropathy)

Design outcomes

Primary

MeasureTime frame
Mean score of self-care activities. Timepoint: Before the intervention and after completing the intervention in the 36-39 weeks of pregnancy. Method of measurement: Summary of the Diabetes Self-Care Activities (SDSCA).;Diabetes Management Self-Efficacy. Timepoint: Before the intervention and after completing the intervention in the 36-39 weeks of pregnancy. Method of measurement: DMSES= Diabetes Management Self-Efficacy Scale.;Pregnancy Experience. Timepoint: Before the intervention and after completing the intervention in the 36-39 weeks of pregnancy. Method of measurement: Pregnancy Experience Scale (PES).

Secondary

MeasureTime frame
Frequency of preterm labor. Timepoint: Sixth week postpartum based on the medical record. Method of measurement: Maternal and neonatal outcomes checklist.;Frequency of cesarean delivery. Timepoint: Sixth week postpartum based on the medical record. Method of measurement: Maternal and neonatal outcomes checklist.;The frequency of hospitalization of newborns in the intensive care unit. Timepoint: Sixth week postpartum based on the medical record. Method of measurement: Maternal and neonatal outcomes checklist.;Breastfeeding performance score. Timepoint: Sixth week postpartum. Method of measurement: Breastfeeding performance questionnaire.;Satisfaction score of prenatal care. Timepoint: After completing the intervention in 36-39 weeks of pregnancy. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Maghalian

Tabriz University of Medical Sciences

mahsamaghalian@gmail.com+98 41 3475 1708

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026