A Parental Educational Intervention to Facilitate Informed Consent for Pediatric Procedural Sedation 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: NCT01850329|
Recruitment Status : Completed
First Posted : May 9, 2013
Last Update Posted : April 6, 2017
|Condition or disease||Intervention/treatment||Phase|
|Informed Consent Process||Other: computed-assisted information program||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||67 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||A Parental Educational Intervention to Facilitate Informed Consent for Pediatric Procedural Sedation in the Emergency Department|
|Actual Study Start Date :||December 7, 2009|
|Actual Primary Completion Date :||September 9, 2014|
|Actual Study Completion Date :||September 9, 2014|
No Intervention: control
No computed-assisted information program will be administered.
computed-assisted information program will be administered.
Other: computed-assisted information program
- structured questionnaire [ Time Frame: before and immediately after the intervention when participants are in the emergency department, it is expected to take an expected average time of one hour ]a structured questionnaire with knowledge measure and satisfaction will be delivered to the participants for data collection.
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): NCT01850329
|Kaohsiung Medical University Hospital|
|Kaohsiung, Taiwan, 807|