Postpartum Hemorrhage
Conditions
Interventions
This is a randomized clinical trial, with a parallel group, allocated 1:1, randomly, through numbers drawn by a computer program. Experimental group: 98 health professionals who will undergo training
I02.903.847
Sponsors
Faculdade de Enfermagem da Universidade Federal de Goiás
Secretaria da Saúde do Estado de Goiás - Leide das Neves Ferreira
Eligibility
Inclusion criteria
Inclusion criteria: Health professionals in the obstetric area working in direct assistance to parturient and postpartum women and newborns in the following sectors: Obstetric Emergency, Surgical Center, Normal Delivery Unit and Joint Accommodations; be contactable by telephone; have access to the internet at home or on your cell phone; both genders
Exclusion criteria
Exclusion criteria: Health professionals who, during the period of data collection, are on vacation, or on sick leave, or away from care or serving prior notice; professionals who, after three attempts, are not on their original shift according to the duty schedule; professionals who have already participated in a Clinical Simulation course for Postpartum Hemorrhage (PPH)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the knowledge of health professionals, verified using an instrument with objective questions, applied in a pre- and post-test format, based on the observation of a variation of at least 5% in pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to know the satisfaction and self-confidence of health professionals regarding learning, verified using a validated instrument called the Learning Satisfaction and Self-Confidence Scale, of the 5-item Likert type. | — |
Countries
Brazil
Contacts
Public ContactAna Paula Moreira
Universidade Federal de Goiás
Outcome results
None listed