Stress ball squeeze eases pain after heart surgery, study says

NCT ID NCT07251270

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Recruiting now
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
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Cancelled before anyone took part.

Expanded access (not trials)

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First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times

Summary

This study tests if using a stress ball can reduce pain, anxiety, and changes in heart rate during chest tube removal after open heart surgery. About 46 adults who have one chest tube after surgery will be split into two groups: one will squeeze a stress ball during the procedure, and the other will receive standard care. Researchers will measure pain and anxiety levels right after the tube is removed and again 15 and 30 minutes later.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

66 people

The number who actually took part.

Started

Nov 2025

Finished

Jun 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria:Patients will be included : have only one chest tube after open heart surgery, * are 18 years of age or older, * 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). Exclusion Criteria:Patients who do not have a chest tube or have multiple chest tubes after open heart surgery, * Are under 18 years of age, * Are conscious and uncooperative, * Do not speak or understand Turkish, * Are in an unstable general condition or 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) will not be included in the study.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Turkey, Mersin University,

    Yenişehir, Mersin, 33120, Turkey (Türkiye)

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