Influence of Audiovisual Aids in the Preanesthetic Interview | NCT03274336

Studies
Influence of Audiovisual Aids in the Preanesthetic Interview

NCT03274336

Sponsor

Schulthess Klinik

Status

Completed

Last Update Posted

Sep 6, 2017Actual

Enrollment

1,172Actual

Phase

Not Applicable

Conditions

Patient Satisfaction

Interventions

questionnaire
face-to-face interview
brochure
movie

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Aug 2017

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jun 1, 2015Actual

Primary Completion Date

Sep 1, 2015Actual

Completion Date

Sep 30, 2015Actual

First Submitted Date

Aug 19, 2017

First Submission Date that Met QC Criteria

Sep 4, 2017

First Posted Date

Sep 6, 2017Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Sep 4, 2017

Last Update Posted Date

Sep 6, 2017Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief 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.

Detailed Description

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

1,172Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
interview	Active Comparator	questionnaire after face-to-face interview	Behavioral: questionnaire Behavioral: face-to-face interview Behavioral: brochure Behavioral: movie
brochure	Placebo Comparator	questionnaire interview plus brochure	Behavioral: questionnaire Behavioral: brochure
movie	Placebo Comparator	questionnaire interview plus movie	Behavioral: questionnaire Behavioral: movie

Interventions

Name	Type	Description	Arm Group Labels	Other Names
questionnaire	Behavioral	questionnaire post preanesthetic interview	brochure interview movie

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Patient satisfaction on a questionnaire	Patient satisfaction after the preanesthetic interview is measured	15 Minutes

Secondary Outcomes

Measure	Description	Time Frame
time	time needed for the preanesthetic interview in Minutes	30 Minutes

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

voluntary

Exclusion Criteria:

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

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

Not provided

Maximum Age

Not provided

Standard Ages

ChildAdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Name	Affiliation	Role
Berthold Moser, MD	Schulthess Klinik	Principal Investigator

Condition Browse Module

MeSH Terms

ID	Term
D017060	Patient Satisfaction

Ancestor Terms

ID	Term
D000074822	Treatment Adherence and Compliance
D015438	Health Behavior
D001519	Behavior

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D011795	Surveys and Questionnaires
D009040	Motion Pictures

Ancestor Terms

ID	Term
D003625	Data Collection
D004812	Epidemiologic Methods
D008919	Investigative Techniques
D017531	Health Care Evaluation Mechanisms

Browse Leaves

Not provided

Browse Branches

Not provided