Investigating the effect of education and support on improving the reproductive health of pregnant adolescents

InvestigatingThe effect of educational and Supportive intervention on health performance and general self-efficacy of pregnant adolescents

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230816059157N1

Enrollment

136

Registered

2023-08-28

Start date

2023-08-23

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

None listed

Interventions

Intervention 1: Intervention group: Educational class for pregnant teenagers with companions. The course will be held during 6 sessions of 60-90 minutes by the researcher in the conference hall of Val

Eligibility

Sex/Gender

Female

Age

10 Years to 19 Years

Inclusion criteria

Inclusion criteria: Adolescents 10-19 years old Married Pregnant Primigravida 18-24 weeks of pregnancy Having a health file in the health centers of Fasa and its suburbs Having the ability to speak and understand Persian language Informed consent to participate in research Willingness to participate in classes with accompanying attendance

Exclusion criteria

Exclusion criteria: Having a high-risk pregnancy, including diabetes, high blood pressure, and chronic diseases affecting pregnancy such as cardiovascular disease, lung disease, etc., and History or current mental problems Experiencing a catastrophic life event in the past three months Having physical movement restrictions (heart disease, lung disease, incompetent cervix, high-risk multiple pregnancies, continuous bleeding, Placenta Previa after 26 weeks, Gestational blood pressure) Addiction to any kind of drugs, tobacco Receiving special medicine due to a physical or psychological problem

Design outcomes

Primary

Measure	Time frame
Health Performance and General Self-efficacy. Timepoint: Before the intervention - immediately after the end of the intervention - one month after the intervention. Method of measurement: Health practices questionnaire/ General Self-E?cacy Scale (Sherer et al).	—

Secondary

Measure	Time frame
Maternal and newborn outcomes such as high-risk pregnancy, birth weight of the baby, condition of the baby, type of delivery. Timepoint: immediately after child birth. Method of measurement: High-risk pregnancy (with/without), birth weight (Kg), condition of baby(hospitalization/Rooming in), type of delivery (NVD/cesarean section).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFiroozeh Nourimand

Shahroud University of Medical Sciences

firozeh.nourimand@gmail.com+98 71 5333 6950

Outcome results