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Could a simple scheduling change ease heart surgery nerves?

NCT ID NCT06794697

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

About 400 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2024

Expected to finish

May 2027

An estimate. End dates often move.

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.

Who is studied

Patients with cardiac pathology requiring cardiac surgery

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: * 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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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Centre Hospitalier Universitaire de Rennes

    RECRUITING

    Rennes, 35033, France

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