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

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ClinicalTrials.gov Identifier: NCT03344445
Recruitment Status : Unknown
Verified March 2018 by IRB of NTUH Hsin-Chu Branch, National Taiwan University Hospital Hsin-Chu Branch.
Recruitment status was:  Active, not recruiting
First Posted : November 17, 2017
Last Update Posted : March 9, 2018
Sponsor:
Information provided by (Responsible Party):
IRB of NTUH Hsin-Chu Branch, National Taiwan University Hospital Hsin-Chu Branch

Brief Summary:
To investigate the differenec of patients' satisfaction and information gain betweem face-to-face interview and video introduction

Condition or disease Intervention/treatment Phase
Anesthesia Other: video-assisted pre anesthesia explain Not Applicable

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.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 250 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Intervention Model Description: simple compare of information gain between traditional visit and video-assisted visit
Masking: Single (Outcomes Assessor)
Primary Purpose: Other
Official Title: Difference of Information Gain Between Video-base and Doctor Interview After Preanesthetic Visit
Actual Study Start Date : January 1, 2017
Estimated Primary Completion Date : December 31, 2018
Estimated Study Completion Date : December 31, 2018

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.




Primary Outcome Measures :
  1. 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

  2. satification anaylsis [ Time Frame: after every 100 effective data or 1 year, analyzed the data ]
    The score of questionnaire represent the ratification of patient



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03344445


Sponsors and Collaborators
IRB of NTUH Hsin-Chu Branch
Investigators
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Study Chair: Li Kuei Chen, M.D. National Taiwan University Hospital Hsin-Chu Branch
Publications of Results:
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Responsible Party: IRB of NTUH Hsin-Chu Branch, Department of Anesthesia, National Taiwan University Hospital Hsin-Chu Branch
ClinicalTrials.gov Identifier: NCT03344445    
Other Study ID Numbers: 102-019-E
First Posted: November 17, 2017    Key Record Dates
Last Update Posted: March 9, 2018
Last Verified: March 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs