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Early or Late Booster in Basic Life Support for Health Care Professionals

H

Hopital Montfort

Status

Completed

Conditions

Basic Life Support

Treatments

Other: Late Booster Teaching
Other: Early Booster Teaching

Study type

Interventional

Funder types

Other

Identifiers

NCT03893253
18-19-08-020

Details and patient eligibility

About

Attrition of skills after basic life support (BLS) training is common. Psychology studies have established that for basic memory recall tasks, spaced learning strategies improve retention. Spaced learning is often organized as a refresher or 'booster' course after initial training. This study aims to investigate if this principle holds true for BLS skills, which require rapid memory recall and efficient deployment of procedural skills while under time pressure.

Full description

Health care professionals who have not received BLS training in the 6 months leading up to the date of participation will be recruited from local health care institutions in the greater-Ottawa area. Participants will be randomized into one of three groups: early booster, late booster, or no booster (control). Currently, no booster is the educational standard. The early booster group will receive a booster at 3 weeks, the late booster at 2 months, and no booster for the control. All participants will undergo BLS training, an immediate post-test, and a retention post-test at 4 months. Post-tests involve a simulated cardiac arrest scenario. Raters will be blinded to the group allocation and simulation test order.

Enrollment

84 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

-Healthcare professionals who interact with patients and have not received any BLS training or practice in the 6 months leading up to the date of their participation will be recruited.

Exclusion criteria

  • under 18 years of age
  • non healthcare professionals
  • healthcare professionals who don't interact directly with patients
  • healthcare professionals who have completed Basic Life Support training in the previous six months

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

84 participants in 3 patient groups

Early Booster Teaching
Experimental group
Description:
The early booster group will receive a booster teaching session at 3 weeks post-training followed by feedback.
Treatment:
Other: Early Booster Teaching
Late Booster Teaching
Active Comparator group
Description:
The late booster group will receive a booster teaching session at 2 months post-training followed by feedback.
Treatment:
Other: Late Booster Teaching
Control group
No Intervention group
Description:
The control group will receive no booster teaching at all.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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