Skip to content

UNPACK - Evaluation of Patient's Understanding and Cost Effectiveness in the Pre-Anesthetic Clinic - A Multicenter Study on Knowledge Retention and Economic Efficiency

UNPACK - Evaluation of Patient's Understanding and Cost Effectiveness in the Pre-Anesthetic Clinic - A Multicenter Study on Knowledge Retention and Economic Efficiency - UNPACK

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034364
Enrollment
352
Registered
2024-08-12
Start date
2025-06-15
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients scheduled for a pre-anesthesia assessment due to a planned surgery.

Interventions

Group 1: Control Group. The control group receives the standard information sheet. Subsequently, a regular premedication consultation with an anesthesiologist is conducted. Group 2: Test Group. Instea

Sponsors

Klinik für Anästhesiologie, Uniklinikum RWTH Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Adult patients who present at the pre-anesthesia assessment clinic due to a planned surgery or for whom a bedside consultation for a pre-anesthesia assessment has been scheduled by the department of anesthesiology. The indication for surgery and presentation at the pre-anesthesia assessment clinic is based on a medical indication related to an existing illness and is independent of the study. - Signed informed consent. - Clear understanding of the study information.

Exclusion criteria

Exclusion criteria: - Individuals who are dependent of or employed by any of the investigators. - Inability to adhere to the study protocol. - Inability to independently go through and answer the questionnaire. - Individuals who work or have worked in the medical field or in a closely related area (e.g., hospital administration, medical law attorney, etc.), study a medical or medically related field (e.g., biomedicine), or undergo training in a medical field. - Lack of written informed consent or lack of ability to consent. - Individuals who are involuntarily placed in custodial accomodation due to a official order or court order.

Design outcomes

Primary

MeasureTime frame
Percentage of correctly answered questions per patient in relation to the informational materials used. The questionaire was created for this study and was validated in a pilot study.

Secondary

MeasureTime frame
(1) Patient satisfaction with the pre-anesthesia assessment (2) Preoperative Anxiety of the patients (3) Duration of the pre-anesthesia assessment The questionaire was created for this study and was validated in a pilot study. Furthermore, a german Version of the der Amsterdam Preoperative Anxiety and Information Scale (APAIS) is used [1]. [1] Berth H, Petrowski K, Balck F. The Amsterdam Preoperative Anxiety and Information Scale (APAIS) - the first trial of a German version. Psychosoc Med. 2007 Feb 20;4:Doc01.

Countries

Germany

Contacts

Public ContactAnna Fischbach

Klinik für Anästhesiologie, Uniklinikum RWTH Aachen

afischbach@ukaachen.de+492418088179

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026