The Effect of Using a Stress Ball on Pain, Anxiety, and Vital Signs During Breast Biopsy
- NCT ID
- NCT07844395
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- TC Erciyes University
- Conditions
- Anxiety, Breast Biopsy, Procedural Pain, Vital Signs
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 53 participants (Estimated).
What is being studied
- Behavioral: Using a Stress Ball
Who may be eligible
- Ages
- 18 Years to no maximum
- Sex
- Female
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility 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
Study locations
1 study location is listed.
Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.
Countries: Turkey (Türkiye)
Sample of listed locations
- Erciyes University Faculty of Medicine Hospitals — Kayseri, Turkey (Türkiye) — Recruiting
Study details
- Start date
- September 11, 2026
- Primary completion date
- October 11, 2026
- Completion date
- October 31, 2026
- First posted
- September 28, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07844395
- Registry last updated
- September 28, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07844395 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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