A Parental Educational Intervention to Facilitate Informed Consent for Pediatric Procedural Sedation in the Emergency Department
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 67
- Locations
- 2
- Primary Endpoint
- structured questionnaire
Study Overview
Brief Summary
This study is planning to develop the computed-assisted information program and determine whether the computed-assisted information program are superior to routine discussion for informing parents in the emergency department (ED) about risks, benefits, and alternatives to receiving procedural sedation for their children.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Health Services Research
- Masking
- None
Eligibility Criteria
- Ages
- — to 18 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Parents with patients under 18 years of age
- •patients receive the procedural sedation and anesthesia in the emergency department
Exclusion Criteria
- •clinically unstable
- •refuse to participate
- •unable to understand the consent process for this study
Outcomes
Primary Outcomes
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.
Secondary Outcomes
No secondary outcomes reported
Investigators
Yen-Ko Lin (980425)
Attending physician
Kaohsiung Medical University Chung-Ho Memorial Hospital