BridgeMD
Tests treatment safety and results for Adolescent Pregnancy
Official title The Effect of Antenatal Education Based on the Breastfeeding Self-Efficacy Theory and Postpartum Follow-Up Counseling on Breastfeeding Self-Efficacy and Attitudes in Adolescent Pregnant Women
ClinicalTrials.gov ID: NCT07025265
What this study is testing
- What it's testing
- Adolescence is the period between the ages of 10 and 19, during which individuals undergo physiological, biological, psychological, and social development, transitioning from childhood to adulthood. Pregnancies occurring during this period are defined as adolescent pregnancies.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 15 to 19, women only
You may be able to join if
- Adolescent pregnant individuals (ages 14-19)
- Singleton pregnancy
- Gestational age of at least 28 weeks at enrollment
- Planning to breastfeed postpartum
- Willing to participate in antenatal education and postpartum follow-up counseling
You likely can't join if
- Multiple pregnancy (twins, triplets, etc.)
- Maternal or fetal conditions contraindicating breastfeeding (e.g., galactosemia)
- Severe maternal complications (e.g., preeclampsia with severe features, placenta previa with bleeding)
- History of previous breastfeeding difficulties or conditions affecting lactation (e.g., breast surgery)
- Psychiatric disorders that may interfere with participation
- Inability to complete follow-ups due to planned relocation or other reasons
See the full eligibility criteria
- Adolescent pregnant individuals (ages 14-19)
- Singleton pregnancy
- Gestational age of at least 28 weeks at enrollment
- Planning to breastfeed postpartum
- Willing to participate in antenatal education and postpartum follow-up counseling
- Able to provide informed consent
- Multiple pregnancy (twins, triplets, etc.)
- Maternal or fetal conditions contraindicating breastfeeding (e.g., galactosemia)
- Severe maternal complications (e.g., preeclampsia with severe features, placenta previa with bleeding)
- History of previous breastfeeding difficulties or conditions affecting lactation (e.g., breast surgery)
- Psychiatric disorders that may interfere with participation
- Inability to complete follow-ups due to planned relocation or other reasons
The study team makes the final eligibility decision.
Where it's taking place
- Sanliurfa, Şanlıurfa, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 15 years to 19 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Sanliurfa, Şanlıurfa, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.