Could a simple stress ball ease the pain of a heart procedure?
NCT ID NCT07808632
First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time
Summary
Researchers are testing whether squeezing a stress ball during femoral arterial sheath removal after coronary angiography can reduce pain and anxiety and improve patient satisfaction. The trial enrolls 34 adults who had a stent or balloon angioplasty through the femoral artery. Half use a stress ball plus routine care, and half receive routine care alone. The team measures pain, anxiety, satisfaction, and blood pressure and heart rate before and after the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a silicone stress ball squeezed rhythmically during the procedure
- What this could lead to
- If it works, hospitals could add a cheap, drug-free option to make sheath removal after coronary angiography less painful and stressful.
- What could go wrong
- The trial is small, with 34 patients at one center, so any benefit may be modest or may not hold up in larger, more varied groups. A stress ball cannot remove the physical cause of pain from sheath removal.
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
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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
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About 34 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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 who underwent coronary angiography via the femoral artery and received stent implantation or balloon angioplasty * Aged 18 years or older * Willing to participate in the study and providing written informed consent * Conscious, oriented, and cooperative * Able to read and understand Turkish * No hearing or visual impairment that would interfere with participation * Clinically and hemodynamically stable * No diagnosed psychiatric disorder Exclusion Criteria: * Coronary angiography performed via the radial artery * Development of a complication during coronary angiography, such as arrhythmia * Administration of sedation during coronary angiography * Pregnancy * Prisoners or other vulnerable individuals
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Turkey, Mersin University Hospital
Yenişehir, Mersin, 33120, Turkey (Türkiye)
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