Can VAST Improve ACLS in Rwanda
Can the VAST Course Enhance Resuscitation Skills in a Resource-limited Setting?
1 other identifier
interventional
47
1 country
1
Brief Summary
Aim The purpose of this study is to determine if the addition of the VAST Course to technical resuscitation skills training enhances healthcare providers' resuscitation performance in a resource-limited setting. Objectives The aims of this research will be achieved by meeting the following objectives:
- 1.Quantitative evaluation of study participants' resuscitation performance during a simulation scenario before ACLS course, immediately following ACLS course, immediately following VAST course, and at 4 months post training.
- 2.Qualitative exploration of the barriers and supports identified by course participants to implementing resuscitation in the workplace after resuscitation skills training through focus groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 28, 2022
CompletedFirst Posted
Study publicly available on registry
March 14, 2022
CompletedStudy Start
First participant enrolled
May 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2022
CompletedNovember 17, 2022
November 1, 2022
2 months
February 28, 2022
November 13, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Time to initiation of CPR
The time it takes for the team to start chest compressions in the simulation in seconds
From start of simulation scenario to time of first chest compressions, assessment up to 2 minutes of simulation
Secondary Outcomes (2)
Time to epinephrine administration
From start of simulation scenario to time of first epinephrine administration, assessment up to 5 minutes of simulation
Time to defibrillation
From start of simulation scenario to time of first defibrillation, assessment up to 5 minutes of simulation
Study Arms (1)
ACLS and then VAST teaching intervention
EXPERIMENTALFor each hospital, the intervention will be to pair a 2-day technical resuscitation skills training adapted from the ACLS/AHA and a 3-day VAST course for a multidisciplinary team of 20 participants (i.e., nurses, doctors, non-physician anesthesia providers). Participants' resuscitation skills will be tested at 4 time points: immediately before the ACLS course, immediately after the ACLS course, immediately after the VAST Course, and at 4 months post training.
Interventions
Advanced Cardiovascular Life Support (ACLS) is a resuscitation course to teach recognition and treatment of cardiopulmonary arrest in patients.
The Vital Anesthesia Simulation Training (VAST) Course focuses on core clinical practices and non-technical skills needed to respond to the most common urgent and emergent clinical challenges found in hospitals in resource-limited settings like Rwanda.
Eligibility Criteria
You may qualify if:
- Full course participation
- Available for focus group interviews
You may not qualify if:
- Refusal to provide informed consent
- Participated in VAST or ACLS training in the four months prior to study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Torontolead
- University of Rwandacollaborator
- ANZCA Health Equity Projectcollaborator
Study Sites (1)
University of Rwanda
Kigali, Rwanda
Related Publications (1)
Tuyishime E, Mossenson A, Livingston P, Irakoze A, Seneza C, Ndekezi JK, Skelton T. Resuscitation team training in Rwanda: A mixed method study exploring the combination of the VAST course with Advanced Cardiac Life Support training. Resusc Plus. 2023 Jun 16;15:100415. doi: 10.1016/j.resplu.2023.100415. eCollection 2023 Sep.
PMID: 37363124DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Teresa Skelton, MD, FRCPC
University of Toronto
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Anesthesiologist, Assistant Professor
Study Record Dates
First Submitted
February 28, 2022
First Posted
March 14, 2022
Study Start
May 1, 2022
Primary Completion
July 1, 2022
Study Completion
October 1, 2022
Last Updated
November 17, 2022
Record last verified: 2022-11
Data Sharing
- IPD Sharing
- Will not share
Final results will be prepared for publication but no plan to share IPD