Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating preoperative anxiety levels in cardiac surgery patients based on admission day

Official title: Evaluation of Preoperative Anxiety Level Based on the Day of Admission for Cardiac Surgery

Run by Rennes University Hospital · NCT06794697 · Data updated 2026-11-12

This study is trying to see if the day patients are admitted for cardiac surgery affects their anxiety levels before the operation.

More Cardiac Surgery trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment400 (estimated)
SponsorRennes University Hospital
Academic / other
Locations1 site (Rennes)
StatusRecruiting
StartedNovember 12, 2024
Main results expectedMay 2027
Study endsMay 2027
Registry record updatedAugust 7, 2026
Trial IDNCT06794697 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults over 18 years old who are scheduled for elective cardiac surgery and can provide informed consent.

Probably not a fit

Patients undergoing emergency cardiac surgery or those with psychiatric disorders or cognitive impairments may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the impact of the day of admission (either the day before surgery or the day of surgery) on preoperative anxiety levels in patients scheduled for cardiac surgery. Utilizing the Amsterdam Preoperative Anxiety and Information Scale (APAIS), the study will involve 400 patients divided into two groups: those admitted one day prior to surgery and those admitted on the day of surgery. Participants will complete a questionnaire upon admission and just before entering the operating room to measure their anxiety levels. The findings may help identify factors that can be modified to enhance patient care and reduce anxiety.

Why it matters

Potential benefit: If successful, this study could lead to improved management of preoperative anxiety in cardiac surgery patients, enhancing their overall surgical experience.

How similar studies have gone: While there have been studies on preoperative anxiety, this specific evaluation of admission day effects is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Centre Hospitalier Universitaire de Rennes
    Rennes, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.