Implementation of a Computer-based Questionnaire for Preoperative Evaluation in Anesthesia Ambulance

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Completed
CT.gov ID
NCT03243747
Collaborator
(none)
81
1
10
246.5

Study Details

Study Description

Brief Summary

Preanesthetic evaluation is a clinical assessment process with purpose of increased patient safety. One focus is review of patient medical history to reduce perioperative morbidity and mortality as well as optimize the daily process in at anesthesia ambulance. The aim of that study is the development and implementation of a practical computer-based individualized and risk-adapted questionnaire for the daily routine

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The study was a step-by-step process. In the first investigation in 2013 the investigators included 50 patients and 81 patients in 2016. Questionnaires were identical in both testing stages for comparability. Practicability of a computer-based questionnaire on patient medical history, diagnosis as well as behavior guidelines was tested at anesthesia ambulance. Moreover, the investigators evaluated the user satisfaction with the help of a separate anonym paper-based questionnaire in 2013 as well as in 2016.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    81 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Implementation of a Computer-based Questionnaire for Preoperative Evaluation in Anesthesia Ambulance
    Actual Study Start Date :
    Oct 4, 2016
    Actual Primary Completion Date :
    Oct 14, 2016
    Actual Study Completion Date :
    Oct 14, 2016

    Outcome Measures

    Primary Outcome Measures

    1. Utilization of computer-based questionnaire measured by duration time [Time in the outpatient clinic of anesthesia, an average of 1 hour]

    2. Number of assistance during filling-out in depending of age [Time in the outpatient clinic of anesthesia, an average of 1 hour]

    Secondary Outcome Measures

    1. Question 1: All in all I am content [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    2. Question 2: The usability of tablet-pc is easy [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    3. Question 3: My medical history is well determined [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    4. Question 4: The phrasing of questions is clearly understandable [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    5. Question 5: The total count of questions is acceptable [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    6. Question 6: The complete duration time is acceptable [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    7. Question 7: In the future, I would prefer digital questionnaires [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire

    8. Question 8: In the future, I would prefer the questionnaire at home using internet. [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      User satisfaction evaluation by the help of a paper-based questionnaire. The evaluation was based on rating scale: 1=very good, 2=good, 3=satisfactory, 4=sufficient, 5=poor, 6=fail.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 18 years and older

    • Patients who undergo a procedure in anaesthesia and elective surgery

    • German speaking people

    Exclusion Criteria:
    • Emergency surgery

    • American Society of Anesthesiologists (ASA) classification V and VI

    • Patients with guardianship

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Anesthesiology and Operative Intensive Care Medicne Berlin (CCM/CVK) Berlin Germany 10117

    Sponsors and Collaborators

    • Charite University, Berlin, Germany

    Investigators

    • Study Director: Claudia Spies, MD, Prof., Charité - Univsersitätsmedizin Berlin

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Claudia Spies, Clinical Director of the Department of Anesthesiology and Operative Intensive Care Medicine Berlin (CCM, CVK), Charite University, Berlin, Germany
    ClinicalTrials.gov Identifier:
    NCT03243747
    Other Study ID Numbers:
    • WAA
    First Posted:
    Aug 9, 2017
    Last Update Posted:
    Jun 25, 2018
    Last Verified:
    Jun 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Jun 25, 2018