Improving Informed Consent Process for Percutaneous Cholecystostomy in the Emergency Department
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01476319|
Recruitment Status : Completed
First Posted : November 22, 2011
Last Update Posted : April 7, 2017
|Condition or disease||Intervention/treatment||Phase|
|Cholecystitis||Other: video||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||22 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Actual Study Start Date :||November 9, 2009|
|Actual Primary Completion Date :||September 9, 2014|
|Actual Study Completion Date :||September 9, 2014|
|No Intervention: control|
The intervention group includes patients who obtain information about percutaneous cholecystostomy from a video will view at their bedside on a laptop.
- knowledge and satisfaction measure [ Time Frame: immediately after intervention ]One questionnaire will be used as an outcome measure tool. Participants will be asked to complete one questionnaire with knowledge test and satisfaction evaluation with the process of informed consent after the educational sessions.
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): NCT01476319
|Kaohsiung Medical University Chung-Ho Memorial Hospital|
|Kaohsiung, Taiwan, 807|