Could a simple scheduling change ease heart surgery nerves?
NCT ID NCT06794697
First seen Aug 07, 2026 · Last updated Aug 07, 2026
Summary
This study looks at whether patients who come to the hospital the day before their heart surgery feel more or less anxious than those who arrive on the day of the operation. About 400 adults scheduled for cardiac surgery will fill out a questionnaire at two points: when they are admitted and right before they head to the operating room. The goal is to see if the timing of admission influences how anxious patients feel before a major procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Questionnaire including APAIS scale
- What this could lead to
- If a difference is found, hospitals might adjust admission schedules to reduce patient anxiety before cardiac surgery.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Anxiety is subjective and may be influenced by many factors beyond admission timing.
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.
- Participants
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About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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May 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.
Who is studied
Patients with cardiac pathology requiring cardiac surgery
- 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: * Aged over 18 years old * Scheduled for cardiac surgery * Have received written and oral information about the protocol * Admitted to the cardiac and thoracic surgery units * Not opposed to participating in the research. Exclusion Criteria: * Patient undergoing emergency cardiac surgery with no time for reflection * Legal adults under legal protection (guardianship, curators, or legal protection) * Pregnant or breastfeeding women, minors, individuals unable to express consent * Patient on long-term anxiolytic treatment * Patient with psychiatric disorders, cognitive impairments, or central neurological disorders. * Patient already participating in an ongoing study in the department of Thoracic and Cardiovascular Surgery.
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Genom att skicka in godkänner du våra Användarvillkor
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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Centre Hospitalier Universitaire de Rennes
RECRUITINGRennes, 35033, France
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