Influence of Audiovisual Aids in the Preanesthetic Interview

September 4, 2017 updated by: Schulthess Klinik

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

Study Type

Interventional

Enrollment (Actual)

1172

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • voluntary

Exclusion Criteria:

  • language Problems
  • not able to read or write
  • patients does not want to fill out questionnaire

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Berthold Moser, MD, Schulthess Klinik

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2015

Primary Completion (Actual)

September 1, 2015

Study Completion (Actual)

September 30, 2015

Study Registration Dates

First Submitted

August 19, 2017

First Submitted That Met QC Criteria

September 4, 2017

First Posted (Actual)

September 6, 2017

Study Record Updates

Last Update Posted (Actual)

September 6, 2017

Last Update Submitted That Met QC Criteria

September 4, 2017

Last Verified

August 1, 2017

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

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Patient Satisfaction

Clinical Trials on questionnaire

3
Subscribe