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Family safety reporting intervention for Family Reported Errors and Adverse Events (FACES Trial)
N/A
Waitlist Available
Led By Alisa Khan, MD, MPH
Research Sponsored by Boston Children's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
FACES Trial Summary
This study is evaluating whether a new intervention may help reduce medical errors in hospitals.
FACES Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
experience with safety reporting
family safety reporting rates
Secondary outcome measures
hospital safety culture scores
FACES Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Post-intervention armExperimental Treatment1 Intervention
This arm is the post-intervention arm of parents and providers after the family safety reporting bundle has been implemented on the study units.
Group II: Pre-intervention armActive Control1 Intervention
This arm is the pre-intervention arm of parents and providers before the family safety reporting bundle has been implemented.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Family safety reporting intervention
2018
N/A
~990
Find a Location
Who is running the clinical trial?
Boston Children's HospitalLead Sponsor
761 Previous Clinical Trials
5,578,745 Total Patients Enrolled
1 Trials studying Family Reported Errors and Adverse Events
656 Patients Enrolled for Family Reported Errors and Adverse Events
Alisa Khan, MD, MPHPrincipal Investigator - Boston Children's Hospital/Harvard Medical School
Boston Children's Hospital
2 Previous Clinical Trials
15,056 Total Patients Enrolled
1 Trials studying Family Reported Errors and Adverse Events
656 Patients Enrolled for Family Reported Errors and Adverse Events
Frequently Asked Questions
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