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Cherry pits and showers: surprising new weapon against labor pain?

NCT ID NCT07165405

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

150 people

The number who actually took part.

Started

Feb 2025

Finished

Aug 2025

Lead sponsor

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

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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.

Labor Pain Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Istanbul University-Cerrahpaşa

    Istanbul, Büyükçekmece, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.