NCT03151785

Brief Summary

60,000 people suffer an out of hospital cardiac arrest in the United Kingdom (UK) every year. Bystander cardiopulmonary resuscitation (CPR) rates are dismal (30%) compared with places where CPR education is mandatory for all school children (\>50%). Strategies are needed to increase these rates through innovative approaches. Lifesaver (www.life-saver.org.uk) is an immersive interactive programme/application that presents such an opportunity. This study aims to assess the effectiveness of Lifesaver on CPR attitudes, knowledge, skills acquisition and retention in school children. Additionally, it aims to examine whether Lifesaver provides additional benefits in terms of CPR attitudes, knowledge, skills acquisitions and retention in school children when combined with face-to-face BLS training.

Trial Health

100
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2016

Status
completed

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

Study Start

First participant enrolled

January 1, 2016

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 29, 2016

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2016

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
5 months until next milestone

First Posted

Study publicly available on registry

May 12, 2017

Completed
Last Updated

May 12, 2017

Status Verified

May 1, 2017

Enrollment Period

10 months

First QC Date

June 29, 2016

Last Update Submit

May 11, 2017

Conditions

Keywords

CPRSchoolsEducationLifesaver

Outcome Measures

Primary Outcomes (2)

  • Change in Chest compression depth (mm) from day of intervention and at 2 month and 4 month follow up visits.

    Day 0, 2 month, 4 month

  • Change in Chest compression rate from day of intervention and at 2 month and 4 month follow up visits

    Day 0, 2 month, 4 month

Secondary Outcomes (2)

  • Change in CPR attitude measured using an attitudes table questionnaire from baseline to post teaching and testing on Day 0 of intervention and at follow up

    Baseline on Day 0, Post intervention on Day 0 of testing, 2 month, 4 month

  • CPR knowledge test using a questionnaire

    Post intervention on Day 0 of testing, 2 month, 4 month

Study Arms (3)

Face-to-face BLS training

ACTIVE COMPARATOR

Pupils will receive CPR training by standardised face-to-face BLS training only

Other: Face-to-face BLS training

Lifesaver training

ACTIVE COMPARATOR

Pupils will receive CPR training by Lifesaver programme only

Other: Lifesaver training

Lifesaver and Face-to-Face BLS training

ACTIVE COMPARATOR

Pupils will receive CPR training by Lifesaver and standardised face-to-face BLS training

Other: Lifesaver and Face-to-Face BLS training

Interventions

Pupils will receive CPR training by standardised face-to-face BLS training only

Face-to-face BLS training

Pupils will receive CPR training by Lifesaver programme only

Lifesaver training

Pupils will receive CPR training by Lifesaver and standardised face-to-face BLS training

Lifesaver and Face-to-Face BLS training

Eligibility Criteria

Age11 Years - 14 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • All secondary schools in West Midlands
  • Year 8 pupils

You may not qualify if:

  • Participation in British Heart Foundation Heartstart programme
  • Schools with established CPR training programme for Year 8 and unable to substitute their programme with teaching provided by this study
  • Inability to participate in study during allocated timeframe

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Joyce Yeung

    University of Birmingham

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 29, 2016

First Posted

May 12, 2017

Study Start

January 1, 2016

Primary Completion

November 1, 2016

Study Completion

December 1, 2016

Last Updated

May 12, 2017

Record last verified: 2017-05