A Partner's touch: could endorphin massage ease postpartum mood and boost breastfeeding?
NCT ID NCT07726225
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This trial tests whether combining personalized breastfeeding support with partner-assisted endorphin massage can improve mood, breastfeeding confidence, and mother-infant bonding in first-time mothers after a normal vaginal delivery. Participants will be randomly assigned to receive either standard care or the added support and massage. The study aims to see if these simple, low-cost interventions can make the early postpartum period smoother for new families.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sustainable breastfeeding support and partner-assisted endorphin massage
- What this could lead to
- If effective, this approach could offer a simple, drug-free way to boost mood, breastfeeding confidence, and mother-infant bonding after childbirth.
- What could go wrong
- This is a small, early-stage trial with 64 participants, so results may not apply widely. The massage technique relies on partner participation, which may vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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64 people
The number who actually took part.
- Started
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Nov 2025
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Having a normal delivery at a State Hospital * Having given birth for the first time * Having a normal vaginal delivery * Having undergone a first or second-degree episiotomy (incision) * Not having any abnormalities during the delivery process (prolonged labor, meconium aspiration, pathological deceleration, etc.) * Giving birth to a single child, * Having a live-born baby, * The baby being healthy * The mother and baby being together, * Neither the mother nor the baby having a chronic illness * Not having a psychiatric illness and not using psychiatric medication * Living with one's spouse, * Having reading, writing, and comprehension skills in Turkish * Volunteering to participate in the study and signing the informed consent form * Owning an Android phone Exclusion Criteria: * Having undergone an assisted delivery (vacuum, forceps, cesarean section) * Not being in your first pregnancy * Developing complications during labor (prolonged labor, meconium aspiration, pathological deceleration, etc.) * Having undergone a deep episiotomy (incision) * Giving birth to multiple babies * Stillbirth * Having a condition that requires separation from your baby * Being separated from your spouse * Having a chronic illness in yourself and your baby * Having a baby with anomalies * Having a psychiatric illness and using psychiatric medication * Lacking reading, writing, and comprehension skills in Turkish * Refusing to participate in the research * Not having an Android phone Research Termination Criteria * Mother or baby being hospitalized * Partner not applying endorphin massage * Participant withdrawing from the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Mersin University
Mersin, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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