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Effect of a technology on obstetric nurses' knowledge about Stress prevention after trauma in pregnancy, labor and puerperium of women with physical disabilities: clinical trial ?

Effect of educational technology on obstetric nurses' knowledge about post-traumatic Stress prevention in postpartum women with physical disabilities: clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10279hdr
Enrollment
Unknown
Registered
2024-03-14
Start date
2024-02-26
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

Post-traumatic stress disorders

Interventions

This is a two-arm, double-blind, randomized controlled clinical study. Intervention group: 29 obstetric nurses will receive a mobile application-type educational technology. Control group: 29 obstetri
I02.233.332

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Specialist degree in Obstetrics, Women's Health or related; aged 18 or over; both genders; six months of experience in obstetrics; employed at the public maternity hospital selected for the study

Exclusion criteria

Exclusion criteria: In the process of retirement; on leave; termination of contract with the service; in administrative areas of the maternity; have more than one employment relationship between the public maternity hospitals participating in the study from the same government sphere

Design outcomes

Primary

MeasureTime frame
knowledge of obstetric nurses about post-traumatic stress prevention in the post-partum period in women with physical disabilities, measured by pre-test and post-test scores—

Secondary

MeasureTime frame
No secondary outcomes are expected—

Countries

Brazil

Contacts

Public ContactCamila Carvalho

Universidade Federal de Pernambuco

camilafscarvalho@gmail.com+55(84)988075784

Outcome results

None listed

Source: REBEC (via WHO ICTRP)