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Expansion of access to insertion of the copper intrauterine device at the time of delivery using information technology

Digital care lines on immediate postpartum contraception counseling: use of information and communication technologies in reproductive health education. Expansion of access to insertion of the copper intrauterine device at the time of delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4znfspj
Enrollment
Unknown
Registered
2024-09-18
Start date
2023-05-16
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

Pregnancy

Interventions

Sponsors

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
Lead Sponsor
Centro de Referência de Saúde da Mulher de Ribeirão Preto - CRSMRP- Mater
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women with at least one office visit in the pre-natal service of Women's Health Reference Center of Ribeirão Preto – MATER; informed consent form signed if age at least 18 years old or assent form signed if younger than 18 years old (in this case, with a consent form signed by legal guardian)

Exclusion criteria

Exclusion criteria: Patients that do not have access to a mobile phone with internet connection and access to the free messaging app Whatsapp; clinical conditions that impair the comprehension of the videos (such as alcohol and/or drug addiction, psychiatric diseases without adequate medical treatment); patients with medical conditions that are considered to be categories 3 or 4 for the intrauterine device insertion in the immediate postpartum period, according to the World Health Organization; other conditions observed at the moment of childbirth, according to the Women's Health Reference Center of Ribeirão Preto – MATER protocol, will be considered as exclusion criteria, such as the presence of chorioamnionitis, rupture of membranes for longer than 18 hours, uncontrolled postpartum hemorrhage, multiple vaginal lacerations

Design outcomes

Primary

MeasureTime frame
Evaluate the rate of copper intrauterine device insertion in the immediate postpartum period

Secondary

MeasureTime frame
Evaluate the rate of presence in the puerperal office visit for evaluation of the perinatal inserted intrauterine device

Countries

Brazil

Contacts

Public ContactCarolina Vieira

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

carol.sales@usp.br+55-16-3602-2583

Outcome results

None listed

Source: REBEC (via WHO ICTRP)