Cherry pits and showers: surprising new weapon against labor pain?
NCT ID NCT07165405
First seen Jun 26, 2026 · Last updated Sep 01, 2026 · Updated 2 times
Summary
This study tests whether warm sacral massage using cherry pit pouches and partner-assisted showers can reduce pain and improve the birth experience for first-time mothers. 150 women in active labor will be randomly assigned to massage, shower, or standard care. Pain levels and comfort will be measured using surveys.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hot sacral massage with cherry pits and partner-assisted shower
- What this could lead to
- If effective, these simple, drug-free techniques could offer pregnant women more comfort and control during labor without medication.
- What could go wrong
- This is a small, early-stage study with no blinding, so results may be influenced by expectations. The interventions may not significantly reduce pain for all women.
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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150 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Aug 2025
- 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 years and older
- 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: * Volunteering to participate in the study * Expectation of spontaneous vaginal delivery * Estimated fetal weight between 2500-4000 grams by ultrasound * Single fetus and cephalic presentation, * Term pregnancy (between 37-42 weeks of gestation) * Being in the active phase of labor (cervical dilation of 4 cm) * No analgesia or anesthesia used during the first stage of labor, * No skin disease or open wound preventing massage or showering Exclusion Criteria: * Having undergone infertility treatment, * Delivery by cesarean section for any reason during labor, * Being multiparous * Having any systemic, chronic, or neurological disease (Diabetes Mellitus, Hypertension, Thyroid disorders, Multiple Sclerosis, Epilepsy, etc.) * Regular medication use due to any illness, * Active psychiatric treatment (pharmacotherapy/psychotherapy), * Any induction that may affect uterine contractions and dilation, * Any pregnancy complications (such as placenta previa, preeclampsia, premature rupture of membranes, oligohydramnios, and polyhydramnios) * Interventional delivery (forceps, vacuum) * Any problem that hinders communication (such as not knowing Turkish, hearing, speech, and comprehension disorders)
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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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Istanbul University-Cerrahpaşa
Istanbul, Büyükçekmece, Turkey (Türkiye)
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