Stress ball may help women manage labor pain without drugs
NCT ID NCT07451834
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using a stress ball during active labor can reduce pain and improve comfort. 78 pregnant women were split into two groups: one used a stress ball during contractions, the other received standard care. Researchers measured pain, comfort, and self-efficacy before and after birth. The goal was to see if this simple, non-drug method could help women cope better during labor.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stress ball (handheld device)
- What this could lead to
- If it works, this could offer a simple, drug-free way to help women cope with labor pain and feel more in control.
- What could go wrong
- This is a small, completed trial with only 78 participants. The effect may be modest and not apply to all women or birth settings.
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
-
78 people
The number who actually took part.
- Started
-
Jan 2025
- Finished
-
Feb 2026
- 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 to 35 years
- 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 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: * Singleton pregnancies between 37 and 42 weeks of gestation who were in the active phase of labor, * Had no mental or physical disabilities, * Could speak Turkish, * Volunteered to participate in the study. Exclusion Criteria: * Pregnant women with high-risk pregnancies, * Systemic diseases, a history of medical or obstetric complications, * Those using epidural analgesia or pharmacological pain management
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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
-
KTO Karatay University
Karatay, Konya, Turkey (Türkiye)
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