Ireland
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Recruiting Observational

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

NCT06794697 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-11-12
Last updated
2026-08-07

Condition(s) studied

Cardiac Surgery

Investigational drug(s) / intervention(s)

Questionnaire including APAIS scale

Questionnaire including APAIS scale: Patients will complete a questionnaire in two stages : upon admission and just before leaving for the operating room

Study summary

Prospective, observational, non-randomized study that evaluates the impact of the admission day (J-1 vs J-0) on preoperative anxiety in cardiac surgery patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

  • Comparison of the level of anxiety before leaving for the operating room between patients arriving the day before the operation and those arriving on the day of the operation. — Day of scale completion
    Amsterdam Preoperative Anxiety and Information Scale (APAIS) - score 1 to 5 (1=not anxious at all ; 5=extremely anxious)

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier Universitaire de Rennes Rennes France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06794697 on ClinicalTrials.gov ↗ ← All trials in France