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Clinical Trials in Turkey / NCT07150936
Active, not recruiting Not applicable

Effect of Stress Ball Intervention on Psychophysiological Responses During Hernia Surgery: A Randomized Controlled Trial

NCT07150936 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-08-15
Last updated
2025-09-02

Condition(s) studied

Hernia Surgery

Investigational drug(s) / intervention(s)

stress ball application

stress ball application: Participants' demographic information will be collected interview using the Patient Information Form. Approximately 30 minutes before surgery, patients' systolic and diastolic blood pressure, heart rate, respiratory rate, and oxygen saturation will be measured and recorded. Pain severity will also be assessed using the VAS, and anxiety levels will be assessed using the VAS-A and Spielberger Trait Anxiety Scale. Intraoperative Period: All patients will be placed in the supine position on the operating room table. Patients in the intervention group will continue to use the stress ball for 15 minutes during the surgery, as per randomization. All patients will undergo a repeat 15-minute postoperative assessment of vital signs (systolic and diastolic blood pressure, heart rate, respiratory rate, oxygen saturation), pain with a VAS, and anxiety levels with a VAS-A. After the patients are taken to the clinic after the surgery, the same physiological measurements will repeated 10 mnt later

Study summary

The aim of this study is to evaluate the effect of the stress ball applied during hernia surgery on the anxiety level, pain severity and vital signs of patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Be 18 years of age or older, * Willing to undergo surgery for an umbilical hernia, inguinal hernia, or femoral hernia, * Have no hearing or perception problems, * Have no physical disability that would prevent the use of a stress ball, * Be undergoing hernia surgery for the first time. Exclusion Criteria: * Having used analgesic or anxiolytic medication before surgery, * Being switched to general anesthesia during surgery despite planning for local anesthesia, * Having a diagnosed psychiatric disorder, * Being diagnosed with uncontrolled hypertension.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Afsin State Hospital Kahramanmaraş Afşin

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Other trials for the same condition

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 NCT07150936 on ClinicalTrials.gov ↗ ← All trials in Turkey