Patient Survey as a Tool to Quality Assurance and Quality Improvement

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Recruiting
CT.gov ID
NCT02413775
Collaborator
(none)
1,000
1
92
10.9

Study Details

Study Description

Brief Summary

One goal of the investigators of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin is a continuous improvement in the quality of care to the patients. One focus is the freezing preoperatively during surgery, and on the follow-up study to assess the perceived waiting times in the anesthesiology outpatient clinic.

The project aims to quality assurance and quality improvement of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin .

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The primary objective of the survey is to assess the entire perioperative care with particular focus on the development of perceived waiting times in the anesthesiology outpatient clinic, re-evaluation of the preoperative freezing the preoperative thirst, pain, nausea and vomiting after surgery (PONV prophylaxis).

    The survey will be repeated in a three-year interval (approximately 1000 - 2000 patients per survey) to monitor and improve the quality of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin from the patient point of view.

    In order to achieve a meaningful data collection, a response rate of 50 percent should be achieved.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Patient Survey as a Tool to Quality Assurance and Quality Improvement - Department of Anesthesiology and Operative Intensive Care (CCM/CVK), Charité - Universitätsmedizin Berlin
    Actual Study Start Date :
    Apr 1, 2015
    Actual Primary Completion Date :
    Sep 1, 2018
    Anticipated Study Completion Date :
    Dec 1, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Patient satisfaction [Time during hospital stay, an average of 2 weeks]

      Patient satisfaction with the care provided by the staff of the Department of Operative Anesthesiology and Intensive Care Medicine CCM/CVK; Measurement of satisfaction: Yes/No/Partly

    Secondary Outcome Measures

    1. Waiting time in the premedication visit [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Measurement of waiting time: < 15 minutes, 15-30 minutes, 30-60 minutes, > 60 minutes

    2. Friendliness of the staff during the premedication visit [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Measurement of friendliness: Yes/No/Partly

    3. Information provided during the premedication visit by the anesthetist [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Measurement of Information: Yes/No/Partly

    4. Response to questions during the premedication visit [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Response to questions is measured: Yes/No/Partly

    5. Fear reduction during the premedication visit [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Fear reduction is measured: Yes/No/Partly

    6. Information provided during the premedication visit by educational films [Time in the outpatient clinic of anesthesia, an average of 1 hour]

      Measurement of information by educational films: Yes/No/Partly/No film

    7. Compliance with the planned start of the operation [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Measurement of compliance with the start of the operation: Yes/No

    8. Friendliness of staff [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Measurement of friendliness: Yes/No/Partly

    9. Fear [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Fear measured: Yes, very much/Yes, but not much/No fear /Partly

    10. Thirst [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Thirst measured: Yes, very much/Yes, but not much/No thirst/Partly

    11. Pain [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Pain measured: Yes, strong pain/Yes, but not strong/No pain/Can't remember

    12. Sufficient pain treatment [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Sufficient pain treatment measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No pain/No treatment wanted/Partly

    13. Shivering [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Shivering is measured: Yes, strong/Yes, but not strong/No shivering/Partly

    14. Sufficient therapy in case of shivering [Time in the operation room before start of anesthesia, an average of 30 minutes]

      Sufficient therapy in case of shivering is measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No shivering/No treatment wanted/ Partly

    15. Friendliness of staff [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Friendliness is measured: Yes/No/Partly

    16. Post-operative nausea and vomiting (PONV) [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Measurement of PONV: nausea/vomiting/nausea and vomiting/neither nor

    17. Sufficient therapy in case of PONV [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Sufficient therapy is measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No PONV/No treatment wanted/Partly

    18. Pain intensity [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Pain intensity is measured by likert scale: strong, moderate, low, none

    19. Sufficient therapy in case of pain [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Sufficient therapy is measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No pain/No treatment wanted/Partly

    20. Shivering [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Sufficient therapy in case of shivering is measured: Yes/No/Partly

    21. Sufficient therapy in case of shivering [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Sufficient therapy in case of shivering is measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No shivering/No treatment wanted/Partly

    22. Post-operative nausea and vomiting (PONV) [Time during hospital stay, an average of 2 weeks]

      Measurement of PONV: nausea/vomiting/nausea and vomiting/neither nor

    23. Regional anaesthesia [Time during hospital stay, an average of 2 weeks]

      Measured: Yes / No

    24. Satisfaction with regional anaesthesia [Time during hospital stay, an average of 2 weeks]

      Measurement of satisfaction: Yes/No/Partly

    25. In case of need choosing of regional anaesthesia again [Time during hospital stay, an average of 2 weeks]

      Measurement of choosing again: Yes/No/Perhaps

    26. Satisfaction of care through pain service [Time during hospital stay, an average of 2 weeks]

      Measurement of care through pain service: Yes/No/Partly

    27. Recommendation of medical care (provided by the staff from the Department of Anesthesiology and Intensive Care CVK/CCM) [Time during hospital stay, an average of 2 weeks]

      Measurement of recommendation: Yes/No/Partly

    28. Atmosphere [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Measurement of atmosphere: calm/busy/can´t remember

    29. Postoperative fear [Time in the intensive care unit or post anesthesia care unit, an average of 3 days]

      Measurement of fear: Yes, very much/Yes, but not much/No fear

    30. Postoperative pain [Time during hospital stay, an average of 2 weeks]

      Pain intensity is measured by likert scale: strong, moderate, low, none

    31. Sufficient therapy in case of pain [Time during hospital stay, an average of 2 weeks]

      Sufficient therapy is measured: Yes, sufficiently treated/ Treated, but not sufficiently/Not treated/No pain/No treatment wanted/Partly

    32. Postoperative patient controlled analgesia [Time during hospital stay, an average of 2 weeks]

      Measurement: Yes/No/I don´t know

    33. Choosing of Patient controlled anesthesia [Time during hospital stay, an average of 2 weeks]

      Question: Would you choose patient controlled anesthesia again? Answer: Yes/No/Maybe

    Other Outcome Measures

    1. Postoperative stay [Time during hospital stay, an average of 2 weeks]

      Postoperative stay is measured by: in post anesthesia care unit/intensive care unit/unknown

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • male and female patients who underwent a procedure in anesthesia and willing to take part in the Survey

    • aged >= 1 years

    Exclusion Criteria:
    • unconscious patients,

    • refusal by patient / parents

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Anesthesiology and Intensive Care Medicine CCM and CVK, Charité - University Medicine Berlin Berlin Germany 13353

    Sponsors and Collaborators

    • Charite University, Berlin, Germany

    Investigators

    • Study Director: Claudia Spies, MD, Prof., Charite University, Berlin, Germany

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Claudia Spies, Clinic Director of the Department of Anesthesiology and Operative Intensive Care Medicine, CCM/CVK, Charite University, Berlin, Germany
    ClinicalTrials.gov Identifier:
    NCT02413775
    Other Study ID Numbers:
    • QM-Patient survey
    First Posted:
    Apr 10, 2015
    Last Update Posted:
    Mar 25, 2021
    Last Verified:
    Mar 1, 2021

    Study Results

    No Results Posted as of Mar 25, 2021