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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03274336
Other study ID # Schulthess_Anä_12
Secondary ID
Status Completed
Phase N/A
First received August 19, 2017
Last updated September 4, 2017
Start date June 1, 2015
Est. completion date September 30, 2015

Study information

Verified date August 2017
Source Schulthess Klinik
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 1172
Est. completion date September 30, 2015
Est. primary completion date September 1, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- voluntary

Exclusion Criteria:

- language Problems

- not able to read or write

- patients does not want to fill out questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
questionnaire
questionnaire post preanesthetic interview
face-to-face interview
Group A = face-to-face interview
brochure
after reading a brochure a face to face interview will take place
movie
after seeing a film about the procedure a face-to-face interview will take place

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Schulthess Klinik

Outcome

Type Measure Description Time frame Safety issue
Primary Patient satisfaction on a questionnaire Patient satisfaction after the preanesthetic interview is measured 15 Minutes
Secondary time time needed for the preanesthetic interview in Minutes 30 Minutes
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