Actively Recruiting
Effect of Stress Ball During Chest Tube Removal After Open Heart Surgery
Led by Mersin University · Updated on 2025-12-08
46
Participants Needed
1
Research Sites
29 weeks
Total Duration
On this page
Sponsors
M
Mersin University
Lead Sponsor
M
Mersin University, School of Medicine
Collaborating Sponsor
AI-Summary
What this Trial Is About
15 minutes before the procedure, nurses (FEÖ and NT) will explain and demonstrate how to use the stress ball. The stress ball will be applied for approximately five minutes, including the chest tube removal procedure. A round, medium-hard, high-quality silicone ball, approximately 6 cm in diameter, will be used. Patients will be asked to hold the ball in their palms, count to three, squeeze, and release once. Patients will be instructed to continue this exercise until the chest tube removal procedure is completed, and then, under the supervision of the researcher, for approximately five minutes, focusing their attention on the stress ball. The ball will be washed and cleaned after each use and wiped with disposable asepsis wipes before being administered to the patient. The control group will not receive any other treatment beyond routine treatment and will be assessed at the same time as the study group. The chest tube will be removed by a physician during the stress ball application. Procedural pain level, anxiety level and hemodynamic variables of all patients in the study and control groups will be re-evaluated immediately after chest tube removal and 15 and 30 minutes after chest tube removal.
CONDITIONS
Official Title
Effect of Stress Ball During Chest Tube Removal After Open Heart Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older
- Have only one chest tube after open heart surgery
- Are conscious and cooperative
- Speak and understand Turkish
- Have a stable general condition and hemodynamic variables
- Have a planned surgical procedure
- Have no previous chest tube experience
- Have no psychiatric diagnosis
- Are not using psychiatric and/or local neuromuscular blocking medications
- Agree to participate in the study (sign the Informed Consent Form)
You will not qualify if you...
- Patients under 18 years of age
- Do not have a chest tube or have multiple chest tubes after open heart surgery
- Are conscious and uncooperative
- Do not speak or understand Turkish
- Are in an unstable general condition or have unstable hemodynamic variables
- Have undergone emergency surgery
- Have previous chest tube placement experience
- Have a current psychiatric diagnosis
- Are taking psychiatric and/or local neuromuscular blocking medications
- Do not agree to participate in the study (do not sign the Informed Consent Form)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Turkey, Mersin University,
Yenişehir, Mersin, Turkey (Türkiye), 33120
Actively Recruiting
Research Team
T
Tuğba ÇAM YANIK
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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