Contraception, contraceptive counseling, Routine postpartum follow-up, Postpartum
Conditions
Interventions
This is an open-label, randomized, controlled, parallel superiority clinical trial. Only the statistician will be blinded during data analysis. Postpartum women who opt for the use of the Etonogestrel
V03.175.500
H02.403.840
Sponsors
Faculdade de Odontologia de Bauru da Universidade de São Paulo
Faculdade de Odontologia de Bauru da Universidade de São Paulo
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Postpartum women who have given birth at the Santa Isabel Maternity Hospital; aged between 18 and 45 years; who express a desire to use the Etonogestrel implant after contraceptive instructions; who regularly have access to cell phones with the ability to receive video messages
Exclusion criteria
Exclusion criteria: Patients who do not have a mobile phone with access to the internet and the free WhatsApp messaging application; women with clinical conditions that hinder understanding of the video (addiction to the use of alcohol and/or illicit drugs, vision or hearing difficulties, psychiatric illnesses without adequate clinical treatment); homeless women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Higher satisfaction rates are expected after 1 year of use of the Etonogestrel Implant in the group that received ongoing guidance through educational videos and telemedicine, assessed by satisfaction assessment questionnaires | — |
Secondary
| Measure | Time frame |
|---|---|
| Higher one-year continuation rates of Etonogestrel Implant use are expected in the group that received ongoing counseling through educational videos and telemedicine, evaluating the number of patients who maintain use of the method in 1 year | — |
Countries
Brazil
Contacts
Public ContactMariane Nadai
Faculdade de Odontologia de Bauru
Outcome results
None listed