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Online teaching of caring for the cardiac critical child: A Pilot Study

Teaching pediatric cardiac critical care online: a pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-102g78kb
Enrollment
Unknown
Registered
2022-03-08
Start date
2022-09-16
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Disease

Interventions

Intervention group (40 students) will be invited to attend asynchronous online lectures about pediatric cardiac critical care + synchronous online bi-weekly lectures based on active learning methodolo

Sponsors

Faculdade de Medicina da Universidade de São Paulo
Lead Sponsor
Escola de educação permanente do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Last year residents of pediatric cardiology or pediatric intensive care or neonatology; voluntarily willing to participate

Exclusion criteria

Exclusion criteria: Refusal to participate; refusal to sign the informed consent

Design outcomes

Primary

MeasureTime frame
Expected endpoint 1 is the comparison of knowledge progression throughout the course, between both groups. We hope to evaluate the progression difference within each module between both groups, using the percentual difference between pre and post-test scores, applying an appropriate statistical test according to normality distribution (paired t-student if normal). We expect to refute the null hypothesis and find a statistically significant difference, considered as p<0.05

Secondary

MeasureTime frame
Expected endpoint 2 is the comparison of final course scores between groups. The final score will be an average of all post-test scores. We will compare final scores applying an appropriate statistical test according to normality distribution (t-student test if normal). We expect to refute the null hypothesis and find a statistically significant difference, considered as p<0.05;Expected endpoint 3 is the comparison of satisfaction scores about the course, between both groups. We will evaluate satisfaction using a likert scale based on the NPS (Net Promoter Score). We will compare satisfaction scores applying an appropriate statistical test according to normality distribution (t-student test if normal). We expect to refute the null hypothesis and find a statistically significant difference, considered as p<0.05 ;Expected endpoint 4 is the comparison between usability scores for the learning management system, evaluated with the System Usability Scale. We will compare usability scores applying an appropriate statistical test according to normality distribution (t-student test if normal). We expect not to refute the null hypothesis, since the learning management system is the same for both groups, and find no statistically significant difference

Countries

Brazil

Contacts

Public ContactCarolina Vieira de Campos

Instituto do coração da Faculdade de Medicina da Universidade de São Paulo

carolina.campos@hc.fm.usp.br+551126615339

Outcome results

None listed

Source: REBEC (via WHO ICTRP)