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Study identifier: NCT07410949 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Postpartum Acupressure Education and Breastfeeding Outcomes

Condition: Breastfeeding · Lactation · Postpartum Period  ·  Sponsor: Nigde Omer Halisdemir University

PhaseNA
Planned participants360
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersYes

About this study

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. Participants will be followed for 12 months to assess breastfeeding continuation, breastfeeding self-efficacy, breastfeeding quality, and breastfeeding-related outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Pınar Erdoğan, Assoc. Prof.  ·  +905233646954  ·  drpinarerdogan@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Niğde Ömer Halisdemir University HospitalNiğde, Merkez, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07410949