CompletedNot Applicable

Effects of Breast Intervention During the Late Pregnancy on the Parturients' Breast Engorgement,Maternal Competence,and Stress

Taiwan160 participantsStarted 2023-08-01

Plain-language summary

The study purpose is to examine the effects of breast tenderness relief intervention during the late pregnancy on the parturients' breast engorgement, lactation, breastfeeding, maternal competence, and stress.

Who can participate

Age range20 Years

SexFEMALE

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Exclusion criteria

✕. Pregnant women with a history of smoking, alcohol, and drug abuse;
✕. Pregnant women have mental illness;
✕. Maternal complications during childbirth or postpartum, such as: postpartum hemorrhage, infection, etc.;
✕. Newborns with congenital abnormalities and major diseases;
✕. Pregnant women who are unable or unwilling to breastfeed due to illness or other factors;
✕. Refuse to accept breast compression intervention will be excluded from participating in the study

What they're measuring

breast engorgement

Timeframe: Change from Baseline breast engorgement at 12 weeks after delivery.

The volume and speed of lactation

Timeframe: Change from Baseline lactation at 12 weeks after delivery.

Breastfeeding Self-efficacy Scale Short Form

Timeframe: Change from Baseline Breastfeeding Self-efficacy at 12 weeks after delivery.

Parental Self-efficacy Scale

Timeframe: Change from Baseline Parental self-efficacy at 12 weeks after delivery.

Perceived Stress Scale

Timeframe: Change from Baseline Perceived Stress Scale at 12 weeks after delivery.

Trial details

NCT IDNCT05796284

SponsorNational Defense Medical Center, Taiwan

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-07-31

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