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Postpartum Acupressure Education and Breastfeeding Outcomes

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Recruitment opened
    • Start date changed from estimate of Feb 15, 2026 to Apr 25, 2026
    • Site details revised
    v3
  2. Secondary endpoints: details revised at 2 of 7 entries
    • Study description revised
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07410949
Lead Sponsor Nigde Omer Halisdemir University
Conditions
(from sponsor)		 Breastfeeding, Lactation, Postpartum Period
Related terms Breast Feeding
Enrollment 360 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov