A 15-Minute audio break: could guided imagery soothe heart patients?
NCT ID NCT07794358
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This trial tests whether guided imagery, a relaxation technique using audio recordings, can reduce anxiety and improve sleep and comfort in adults with acute coronary syndrome, such as a heart attack, who are in a cardiac intensive care unit. Participants will be randomly assigned to receive either routine care or routine care plus guided imagery sessions twice a day for two days. Researchers will compare changes in anxiety, sleep quality, and comfort between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Guided imagery, a relaxation technique using audio recordings that lead the listener through calming visualizations and breathing exercises
- What this could lead to
- If it works, guided imagery could become a simple, drug-free way to ease anxiety and improve sleep and comfort for people recovering from heart attacks in intensive care.
- What could go wrong
- This is a small, short-term trial, so the results may not apply to all heart patients. The effect may be modest, and the study does not measure long-term outcomes.
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 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 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: * Age 18 years or older. * Diagnosed with acute coronary syndrome, specifically ST-elevation myocardial infarction (STEMI) or non-ST-elevation myocardial infarction (NSTEMI). * Admitted to and monitored in the cardiac intensive care unit. * Expected to remain in the cardiac intensive care unit for at least two nights and to be transferred to a ward or discharged after the two-day study period. * Clinically and hemodynamically stable, with no ongoing or increasing chest pain, significant respiratory distress, unstable vital signs, symptomatic serious arrhythmia, or need for urgent invasive intervention. * Conscious, oriented to person, place, and time, and able to communicate verbally. * Able to understand and speak Turkish. * No hearing impairment that would prevent listening to the guided imagery audio recording through headphones. * Sufficient cognitive ability to understand and respond to the study questionnaires. * Willing to participate and able to provide written informed consent. Exclusion Criteria: * Diagnosis of unstable angina pectoris. * Confusion, delirium, or any alteration in consciousness that interferes with communication. * Diagnosed dementia or cognitive impairment that prevents understanding study instructions. * Hearing loss that prevents following the audio instructions through headphones. * Inability to communicate verbally. * Clinical or hemodynamic instability, including ongoing chest pain, significant dyspnea, hemodynamic instability, symptomatic serious arrhythmia, or need for urgent intervention. * Receiving invasive mechanical ventilation or respiratory support that interferes with communication. * Receiving sedative treatment at a level that interferes with consciousness or communication. * Active psychosis, severe agitation, or an active psychiatric disorder that prevents following the guided imagery instructions. * Expected cardiac intensive care unit stay of less than two nights. * Refusal to participate or inability to provide informed consent.
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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 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.
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