Difference of Information Gain Between Video-base and Doctor Interview After Preanesthetic Visit
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| ClinicalTrials.gov Identifier: NCT03344445 |
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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
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Anesthesia | Other: video-assisted pre anesthesia explain | Not Applicable |
| 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 |
|---|---|
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No Intervention: traditional vist
Patients receive traditional anesthesiologist visit
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Experimental: video-assisted
Patients watch the video, then an anesthesiologist visit
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Other: video-assisted pre anesthesia explain
Anesthesiologist will visit all study patients, and only the experimental group will read the video. |
- 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
- satification anaylsis [ Time Frame: after every 100 effective data or 1 year, analyzed the data ]The score of questionnaire represent the ratification of patient
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
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
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
| Study Chair: | Li Kuei Chen, M.D. | National Taiwan University Hospital Hsin-Chu Branch |
| 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 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Anesthetics Central Nervous System Depressants Physiological Effects of Drugs |

