Using a stress ball during a breast biopsy
Official title: The Effect of Using a Stress Ball on Pain, Anxiety, and Vital Signs During Breast Biopsy
Run by TC Erciyes University · NCT07844395 · Data updated 2026-11-12
We’re testing whether using a stress ball during a breast biopsy helps reduce pain and anxiety and stabilizes vital signs in patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 53 (estimated) |
| Sponsor | TC Erciyes University Academic / other |
| Locations | 1 site (Kayseri) |
| Status | Recruiting |
| Started | September 11, 2026 |
| Main results expected | October 11, 2026 |
| Study ends | October 31, 2026 |
| Registry record updated | September 28, 2026 |
| Trial ID | NCT07844395 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Female adults 18 or older scheduled for a first-time Tru-Cut breast biopsy, able to speak Turkish, not pregnant or breastfeeding, with no cognitive or communicative impairments and able to use their hands.
✕Probably not a fit
Patients with severe baseline anxiety disorders, chronic pain conditions, daytime analgesic use, or inability to grip the stress ball may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study compares the use of a stress ball during Tru-Cut breast biopsies to standard care. Participants are adults who are having their first breast biopsy and speak Turkish, randomized to either the stress ball intervention or usual procedure without the ball. Pain, anxiety, and vital signs such as heart rate and blood pressure are measured and compared between groups. The goal is to see if this simple nursing tool can improve procedural comfort and physiological stability without adding risk.
Why it matters
Potential benefit: If effective, patients may experience less pain and anxiety during biopsy and more stable vital signs.
How similar studies have gone: Nonpharmacologic distraction and coping strategies have shown promise in reducing procedural distress in various settings, supporting feasibility of this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Scheduled for Tru-Cut breast biopsy * Aged 18 years and older * Undergoing breast biopsy for the first time * Able to speak Turkish * Female sex * Not pregnant * Not breastfeeding * No cognitive, verbal, or hearing impairments that could impede communication * Voluntarily agreeing to participate in the study with written and verbal informed consent Exclusion Criteria: * Chronic pain disorders or regular use of analgesics * Having taken analgesic medication on the day of the procedure * Inability to use the hands or impaired grip/grasp function
Where it's running
-
Erciyes University Faculty of Medicine Hospitals
Kayseri, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Evrim Bayraktar, Assoc. Prof. Dr.
- Email: ealbayrak@erciyes.edu.tr
- Phone: +905332156825
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.