NCT02998723

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
95

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2016

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 6, 2016

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 20, 2016

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2017

Completed
Last Updated

September 7, 2018

Status Verified

September 1, 2018

Enrollment Period

5 months

First QC Date

December 6, 2016

Last Update Submit

September 6, 2018

Conditions

Keywords

Basic Life SupportEducation, MedicalCardiopulmonary ResuscitationLearning

Outcome Measures

Primary Outcomes (1)

  • Basic Life Support performance, as measured by the standardized Heart and Stroke Heartsaver checklist

    BLS performance, as measured by the standardized Heart and Stroke Heartsaver checklist

    4 months

Secondary Outcomes (7)

  • Time to start chest compression;

    4 months

  • Accuracy of compression depth

    4 months

  • Compression ratio

    4 months

  • Hand position

    4 months

  • Tidal volume

    4 months

  • +2 more secondary outcomes

Study Arms (3)

Early Booster Teaching

EXPERIMENTAL

The early booster group will receive a booster teaching session at 3 weeks post-training followed by feedback.

Other: Early Booster Teaching

Late booster Teaching

ACTIVE COMPARATOR

The late booster group will receive a booster teaching session at 2 months post-training followed by feedback.

Other: Late Booster Teaching

Control group

NO INTERVENTION

The control group will receive no booster at all.

Interventions

The early booster group will receive a booster teaching session at 3 weeks post-training followed by feedback.

Early Booster Teaching

The late booster group will receive a booster teaching session at 2 months post-training followed by feedback

Late booster Teaching

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Laypeople who have not received any BLS training or practice in the 6 months leading up to the date of their participation will be recruited.

You may not qualify if:

  • Under 18 years old;
  • Non layperson and Basic Life Training in less than 6 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Ottawa Hospital

Ottawa, Ontario, K1Y4E9, Canada

Location

Related Publications (1)

  • Boet S, Waldolf R, Bould C, Lam S, Burns JK, Moffett S, McBride G, Ramsay T, Bould MD. Early or late booster for basic life support skill for laypeople: a simulation-based randomized controlled trial. CJEM. 2022 Jun;24(4):408-418. doi: 10.1007/s43678-022-00291-3. Epub 2022 Apr 19.

Study Officials

  • Sylvain Boet, MD

    The Ottawa Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 6, 2016

First Posted

December 20, 2016

Study Start

November 1, 2016

Primary Completion

April 1, 2017

Study Completion

April 1, 2017

Last Updated

September 7, 2018

Record last verified: 2018-09

Data Sharing

IPD Sharing
Will not share

Locations