- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03274336
Influence of Audiovisual Aids in the Preanesthetic Interview
Influence of Audiovisual Aids in the Preanesthetic Interview: A Comparison of the Effect of Face-to-face-interview Versus a Brochure and Video Assisted Interview
1000 patients will be asked to fill out a questionnaire about preanesthetic visit right after the interview. On a daily randomization the Groups will be assigned to: Group A = face-to-face interview; Group B = interview plus brochure, Group C= interview plus movie.
Evaluation of patient satisfaction und knowledge transfer will be evaluated with a questionnaire filled out right after the interview with the anesthesist.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- voluntary
Exclusion Criteria:
- language Problems
- not able to read or write
- patients does not want to fill out questionnaire
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: interview
questionnaire after face-to-face interview
|
questionnaire post preanesthetic interview
Group A = face-to-face interview
after reading a brochure a face to face interview will take place
after seeing a film about the procedure a face-to-face interview will take place
|
Placebo Comparator: brochure
questionnaire interview plus brochure
|
questionnaire post preanesthetic interview
after reading a brochure a face to face interview will take place
|
Placebo Comparator: movie
questionnaire interview plus movie
|
questionnaire post preanesthetic interview
after seeing a film about the procedure a face-to-face interview will take place
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient satisfaction on a questionnaire
Time Frame: 15 Minutes
|
Patient satisfaction after the preanesthetic interview is measured
|
15 Minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
time
Time Frame: 30 Minutes
|
time needed for the preanesthetic interview in Minutes
|
30 Minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Berthold Moser, MD, Schulthess Klinik
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Schulthess_Anä_12
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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