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FACETS: Pediatric Resuscitation for Family-centered Care in Pediatric Resuscitation
N/A
Waitlist Available
Led By Nancy Kassam-Adams, PhD
Research Sponsored by Children's Hospital of Philadelphia
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 in situ simulations conducted immediately before and after training.
Awards & highlights
Study Summary
This trial will assess the impact of an online skills training module on providers' confidence and comfort with family centered care, as well as team performance of FCC and resuscitative care skills during simulated pediatric resuscitation scenarios.
Who is the study for?
This trial is for healthcare providers aged 18 or older who work in emergency departments and regularly participate in pediatric resuscitations. There are no specific exclusions, as long as they can perform simulations and understand English well enough to complete online training.Check my eligibility
What is being tested?
The study is testing an online training module called FACETS aimed at improving providers' confidence, comfort, and practice of family-centered care during pediatric resuscitation. It's a randomized controlled trial comparing the effects of this training with usual control conditions.See study design
What are the potential side effects?
Since this trial involves educational interventions rather than medical treatments, there are no direct physical side effects expected from participating in the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre-training survey up to 4 weeks prior to training, post-training survey up to 6 weeks after training
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-training survey up to 4 weeks prior to training, post-training survey up to 6 weeks after training
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pre- to post-training changes in individual providers' self-rated confidence in providing FCC in pediatric resuscitation
Pre- to post-training changes in self-reported use of FCC skills in practice
Secondary outcome measures
Pre- to post-training changes in team performance of FCC
Other outcome measures
Pre- to post-training changes in resuscitative care
Pre- to post-training changes in resuscitative care and in teamwork / team performance
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Family-centered & Trauma-informed Support in Pediatric Resuscitation (FACETS: Pediatric Resuscitation) is an online skills training module for health care professionals involved in pediatric resuscitation in general EDs. The module combines didactic information and scenario-based learning with opportunities for the learner to practice applying their knowledge of Family Centered Care (FCC) practices at key choice points in realistic pediatric resuscitation case scenarios. Training content is guided by evidence regarding FCC practices that are effective in reducing concurrent and ongoing emotional distress in children and family members, and in promoting child and family involvement and satisfaction with care.
Group II: ControlActive Control1 Intervention
An online training module in which participants will receive information and policy education about national pediatric readiness standards for all EDs, including a brief mention of FCC as one of these standards, with no specific skills training in FCC. The module provides practice-relevant knowledge related to pediatric differences and pediatric readiness.
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Who is running the clinical trial?
Children's Hospital of PhiladelphiaLead Sponsor
707 Previous Clinical Trials
8,580,491 Total Patients Enrolled
Yale UniversityOTHER
1,847 Previous Clinical Trials
2,735,728 Total Patients Enrolled
Nancy Kassam-Adams, PhDPrincipal InvestigatorChildren's Hospital of Philadelphia
3 Previous Clinical Trials
694 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Control
- Group 2: Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
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