Difference of Information Gain Between Video-base and Doctor Interview After Preanesthetic Visit

March 7, 2018 updated by: IRB of NTUH Hsin-Chu Branch
To investigate the differenec of patients' satisfaction and information gain betweem face-to-face interview and video introduction

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

We made up a video which showed the type, the method, the risk, and the benefit of all anesthesia with words, pictures, and image. A study nurse will ask the will of patients. The patients enrolled in the study will be randomly divided into traditional group(control group) and study group(study group). The study group will watch the video at first, then our anesthesiologist visit the patient. The control group will receive traditional anesthesiologist visit. After doctors' visit, the patients have to complete a test and a questionnaire. The patients who don't participate in the study will have traditional visit and no test.

Study Type

Interventional

Enrollment (Anticipated)

250

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

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All adult patients were included who were scheduled to undergo elective surgery

Exclusion Criteria:

  • Postoperative stay in the intensive care unit was expected or unexpected.,Repeated general anesthesia had been performed in the previous 6 months,ASA classification was more than or equal to III,There were pronounced cognitive and or speech barriers

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: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: SINGLE_GROUP
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: traditional vist
Patients receive traditional anesthesiologist visit
EXPERIMENTAL: video-assisted
Patients watch the video, then an anesthesiologist visit
Other: video-assisted pre anesthesia explain
Anesthesiologist will visit all study patients, and only the experimental group will read the video.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
inform gain analysis
Time Frame: after every 100 effective data or 1 year, analyzed the data
The score of test would represent the inform gain of patient
after every 100 effective data or 1 year, analyzed the data
satification anaylsis
Time Frame: after every 100 effective data or 1 year, analyzed the data
The score of questionnaire represent the ratification of patient
after every 100 effective data or 1 year, analyzed the data

Collaborators and Investigators

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

Sponsor

IRB of NTUH Hsin-Chu Branch

Investigators

  • Study Chair: Li Kuei Chen, M.D., National Taiwan University Hospital Hsin-Chu Branch

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

January 1, 2017

Primary Completion (ANTICIPATED)

December 31, 2018

Study Completion (ANTICIPATED)

December 31, 2018

Study Registration Dates

First Submitted

November 13, 2017

First Submitted That Met QC Criteria

November 13, 2017

First Posted (ACTUAL)

November 17, 2017

Study Record Updates

Last Update Posted (ACTUAL)

March 9, 2018

Last Update Submitted That Met QC Criteria

March 7, 2018

Last Verified

March 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 102-019-E

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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