- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06003504
The Impact of First Aid Blended Learning Training on Learning Outcomes and Helping Behaviour of Adult Laypeople in Rwanda
The Impact of First Aid Training, Delivered Via a Face-to-face or Blended Learning Approach, on Learning Outcomes and Helping Behaviour of Adult Laypeople in Rwanda: a Randomised Controlled Trial
The goal of this study is to assess the impact of a first aid training delivered through a blended learning approach on learning outcomes and helping behaviour in adult laypeople in Rwanda.
Participants will be randomly assigned to either:
- a first aid training with blended learning approach;
- a first aid training with conventional face-to-face approach;
- no first aid training.
All participants will be asked before, immediately after, and 6 months after the first aid trainings to complete
- a questionnaire on first aid-related knowledge, self-efficacy, and willingness to help;
- a practical test on first aid-related skills.
The helping behaviour of the participants will be surveyed before and 6 months after the first aid trainings have been completed.
Researchers will compare the effects in learning outcomes and helping behaviour after 6 months between:
- the first aid training with blended learning approach and no first aid training;
- the first aid training with blended learning approach and first aid training with conventional face-to-face approach.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Kigali, Rwanda
- Rwanda Red Cross
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adult (≥ 18 years) laypeople
- Access to a smartphone or tablet, which is able to install and run a mobile application
Exclusion Criteria:
- Having attended a first aid training in the past
- Having an academic or professional background in the (para)medical field
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: First aid training with blended learning approach
Participants follow a first aid training delivered through a blended learning approach.
|
The content of the first aid blended learning training is standardised and based on the 2021 edition of the Basic First Aid in Africa manual from the Belgian Red Cross, covering first aid general principles and instructions for:
The training consists of 2 consecutive parts:
Participants get at least 10 days to learn in the mobile application and obtain the admission ticket.
Other Names:
|
Active Comparator: First aid training with face-to-face approach
Participants follow a first aid training delivered through a conventional face-to-face approach.
|
The content of the first aid face-to-face training is standardised and based on the 2021 edition of the Basic First Aid in Africa manual from the Belgian Red Cross, covering first aid general principles and instructions for:
The training consists of a 3-days in-class training with lectures and practical exercises on first aid the-ory and skills, facilitated by a certified first aid instructor of the Rwanda Red Cross.
Other Names:
|
No Intervention: Waitlist control
Participants do not receive any training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
First aid knowledge
Time Frame: Before, immediately after, and 6 months after the first aid trainings
|
20-item multiple choice questionnaire about first aid topics using a numerical scale.
Possible scores range from 0 to 20, with higher scores meaning a better outcome.
|
Before, immediately after, and 6 months after the first aid trainings
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Helping behaviour in the past 6 months
Time Frame: Before and 6 months after the first aid trainings
|
Structured questionnaire to survey the helping behaviour and to gauge the potential barriers and facilitators.
|
Before and 6 months after the first aid trainings
|
First aid skills
Time Frame: Before, immediately after, and 6 months after the first aid trainings
|
22-item observation checklist about first aid practical skills using a numerical scale.
Possible scores range from 0 to 30, with higher scores meaning a better outcome.
|
Before, immediately after, and 6 months after the first aid trainings
|
First aid self-efficacy
Time Frame: Before, immediately after, and 6 months after the first aid trainings
|
10-item scenario-based questionnaire using a 5-point Likert scale assessing self-efficacy concerning first aid topics.
Possible scores range from 0 to 40, with higher scores meaning a better outcome.
|
Before, immediately after, and 6 months after the first aid trainings
|
First aid willingness to help
Time Frame: Before, immediately after, and 6 months after the first aid trainings
|
6-item scenario-based questionnaire using a 5-point Likert scale assessing willingness to help concerning first aid topics.
Possible scores range from 0 to 24, with higher scores meaning a better outcome.
|
Before, immediately after, and 6 months after the first aid trainings
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Costs
Time Frame: Before, immediately after, and 6 months after the first aid trainings
|
Costs associated with a first aid training, relatively to the gain in knowledge.
|
Before, immediately after, and 6 months after the first aid trainings
|
Collaborators and Investigators
Investigators
- Principal Investigator: Emmy De Buck, PhD, Centre for Evidence-Based Practice, Belgium
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FABL-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Emergencies
-
Central Hospital, Nancy, FranceCompleted
-
Betsi Cadwaladr University Health BoardRecruitingMedical EmergenciesUnited Kingdom
-
Technische Universität DresdenCompletedPerformance in Simulated Emergencies | Stress During Simulator Scenario | Behaviour of Physicians in Simulated EmergenciesGermany
-
Universidad de AntioquiaCompleted
-
Second Affiliated Hospital, School of Medicine,...UnknownMedical EmergenciesChina
-
Charite University, Berlin, GermanyZentralinstitut für die Kassenärztliche Versorgung in DeutschlandUnknownNon-urgent EmergenciesGermany
-
Peking University People's HospitalBeijing Emergency Medical Center; Beijing Red Cross Emergency CenterCompletedEmergencies [Disease/Finding]China
-
M.D. Anderson Cancer CenterRecruitingOncologic Complications and EmergenciesUnited States
-
Copenhagen Academy for Medical Education and SimulationCompletedCardiopulmonary Resuscitation | Education | Medical Emergencies
-
Chinese University of Hong KongUnknownEmergencies | Cancer | Oncologic Complications and EmergenciesChina
Clinical Trials on First aid training with blended learning approach
-
ARCIM Institute Academic Research in Complementary...CompletedBurnout | Work-Related StressGermany
-
Sydney Children's Hospitals NetworkCompleted
-
University of OuluUnknown
-
Institut et Haute Ecole de la Santé la SourceHEIG-VD- Haute Ecole d'Ingénierie et de Gestion du Canton de VaudCompletedPreventative MedicineSwitzerland
-
Oregon Center for Applied Science, Inc.Eunice Kennedy Shriver National Institute of Child Health and Human Development...Completed
-
Leanne SaxonInstitute of Public Accountants; Beyond Blue; WorkSafe Victoria; Mental Health...Completed
-
Seattle Children's HospitalRecruitingChild Behavior Problems | Child Disruptive Behavior Disorders | Peer Support | Challenging Behavior | Parent Child Relationship | Positive Parenting | Parent Management TrainingUnited States
-
NYU Langone HealthWithdrawn
-
Zonguldak Bulent Ecevit UniversityNurten TaşdemirCompletedCardiopulmonary Arrest With Successful Resuscitation | Education, NursingTurkey
-
McMaster UniversityHamilton Health Sciences Corporation; Ontario Mental Health Foundation; St. Joseph...CompletedMental Health ImpairmentCanada