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New treatment option for Breastfeeding
Official title Postpartum Acupressure Education and Breastfeeding Outcomes
ClinicalTrials.gov ID: NCT07410949
What this study is testing
- What it's testing
- This randomized controlled trial evaluates whether acupressure education provided to mothers within the first 48 hours postpartum improves exclusive breastfeeding rates at 6 months compared with standard postpartum care alone. Mothers in the intervention group will receive structured education on self-administered acupressure at selected points and will be encouraged to continue home-based practice, while the control group will receive standard breastfeeding support.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, women only. Healthy volunteers may be eligible.
You may be able to join if
- Age 18 to 45 years
- Term singleton birth (≥37 weeks of gestation)
- ≤48 hours postpartum at the time of enrollment
- Intention to breastfeed
- Ability to communicate in Turkish
You likely can't join if
- Contraindications to breastfeeding (e.g., infant galactosemia)
- Severe neonatal condition preventing breastfeeding
- Severe maternal medical or psychiatric condition interfering with breastfeeding
- Current opioid, alcohol, or substance dependence
- Multiple gestation pregnancy
- Severe breast injury or condition within the first 72 hours postpartum preventing breastfeeding
See the full eligibility criteria
- Age 18 to 45 years
- Term singleton birth (≥37 weeks of gestation)
- ≤48 hours postpartum at the time of enrollment
- Intention to breastfeed
- Ability to communicate in Turkish
- Access to a smartphone for educational materials and follow-up reminders
- Willingness to provide written informed consent
- Contraindications to breastfeeding (e.g., infant galactosemia)
- Severe neonatal condition preventing breastfeeding
- Severe maternal medical or psychiatric condition interfering with breastfeeding
- Current opioid, alcohol, or substance dependence
- Multiple gestation pregnancy
- Severe breast injury or condition within the first 72 hours postpartum preventing breastfeeding
The study team makes the final eligibility decision.
Where it's taking place
- Niğde, Merkez, 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, 18 years to 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Niğde, Merkez, 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.