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Stress ball may help women manage labor pain without drugs

NCT ID NCT07451834

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 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

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.

agnosia Labor Pain

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