Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07251270

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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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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