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Squeeze away fear: stress balls tested for mammogram pain

NCT ID NCT07562828

Symptom relief Sponsor: Istanbul University Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Updated 1 time

Summary

This study tests two simple, non-drug methods to help women feel less anxious and in pain during mammograms and breast ultrasounds. One group will squeeze a stress ball before and during the procedure, another will receive calming words and gentle touch, and a third will get standard care. Researchers will measure anxiety and pain levels in 122 first-time participants to see if these approaches help.

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 and empathic verbal communication with therapeutic touch
What this could lead to
If it works, this could offer simple, drug-free ways to make breast imaging less stressful and painful for women.
What could go wrong
This is a small, early-stage trial with no blinding, so results may be influenced by placebo effects or participant expectations.

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

About 122 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Sep 2026

An estimate. End dates often move.

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: * Female participants aged 18 years and older * Scheduled to undergo mammography and breast ultrasonography * Undergoing these imaging procedures for the first time * Literate (able to read and understand study materials) * No sensory or motor impairment affecting the upper extremities (hands/arms) * Willing to participate and able to provide written informed consent Exclusion Criteria: * Previous experience of mammography or breast ultrasonography * Presence of any cognitive impairment that may affect understanding or communication * Presence of any physical disability that may interfere with participation * Hearing or visual impairment that may hinder communication or completion of study procedures * Refusal to participate or inability to provide informed consent

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Conditions

The condition(s) this trial relates to.

Pain, Procedural

As listed by the trial registrant

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

Breast imaging Procedural anxiety Procedural pain

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

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