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Recruiting Not applicable

The Effect of Using a Stress Ball on Pain, Anxiety, and Vital Signs During Breast Biopsy

NCT07844395 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09-11
Last updated
2026-09-28

Condition(s) studied

Breast BiopsyProcedural PainAnxietyVital Signs

Investigational drug(s) / intervention(s)

Using a Stress Ball

Using a Stress Ball: Participants will squeeze a stress ball during the biopsy procedure

Study summary

Breast biopsy is an invasive diagnostic procedure commonly performed for the histopathological diagnosis of breast lesions and can be associated with anxiety and pain. Procedural anxiety and pain may also influence physiological responses, including changes in blood pressure and heart rate. Therefore, non-pharmacological nursing interventions that are simple, low-cost, and easy to implement may be useful in managing procedural distress.

This study aims to investigate the effect of stress ball use during breast biopsy on patients' pain, anxiety, and vital signs. Participants will be assigned to an intervention group using a stress ball during the biopsy procedure or a control group receiving standard care. Pain and anxiety levels, as well as vital signs, will be assessed and compared between the two groups.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Pain Score Assessed by Visual Analog Scale (VAS) — Immediately after the biopsy procedure
    Pain intensity will be evaluated using a 10-cm Visual Analog Scale (VAS) ranging from 0 (no pain) to 10 (worst pain imaginable). Higher scores indicate greater pain intensity.

Trial sites (1)

FacilityCityRegionStatus
Erciyes University Faculty of Medicine Hospitals Kayseri Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07844395 on ClinicalTrials.gov ↗ ← All trials in Turkey