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Clinical Trials/NCT07291466
NCT07291466CompletedNot Applicable

Erhebung Von präoperativer Ängstlichkeit Und Bewertung Beruhigender Maßnahmen: Anonyme Patientenbefragung

Vera Guttenthaler2 sites in 1 country750 target enrollmentStarted: September 30, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
750
Locations
2
Primary Endpoint
Record patients' stated preferences related to anxiety management.

Study Overview

Brief Summary

The aim of this study is to better understand the anxiety of patients before elective surgeries and to investigate which measures for calming are perceived as helpful or pleasant. Adult, German-speaking patients (≥18 years) in the elective surgical setting at UKB are invited to participate. It is planned that at least 400 patients will take part in the survey. The survey is conducted anonymously, voluntarily, and without the collection of personal data. This is a purely observational study without any intervention.

Detailed Description

Patients who come to the premedication outpatient clinic are invited in the waiting area to participate in this anonymous written survey. Participation is voluntary. The survey takes approximately 10-15 minutes. No personal data are collected.

Anxiety is assessed using the State-Trait Operation Anxiety (STOA) and the Amsterdam Preoperative Anxiety and Information Scale (APAIS) questionnaires.

To address anxiety reduction, various possible measures are listed, and patients are asked to check all the options they consider helpful and appropriate. They are also given the opportunity to add further suggestions that are not included in the list.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adults (≥18 years),
  • German-speaking patients
  • elective surgical setting

Exclusion Criteria

  • emergency surgery
  • Patients with documented psychiatric disorders or confusion
  • Individuals admitted under a court or official mandate

Outcomes

Primary Outcomes

Record patients' stated preferences related to anxiety management.

Time Frame: baseline

using multiple-choice and open-ended responses

Secondary Outcomes

  • Assess patients' preoperative anxiety(baseline)

Investigators

Sponsor
Vera Guttenthaler
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Vera Guttenthaler

study coordinator

University of Bonn

Study Sites (2)

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