Mobile technology as an adjunct to postpartum follow-up: a randomized clinical trial.
Not Applicable
- Conditions
- Contraception, Postpartum period
- Registration Number
- RBR-42gv7tq
- Lead Sponsor
- Fundação Bahiana para Desenvolvimento das Ciências - FUNDECI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
Women over 18 years old, immediate postpartum with live newborns; own smartphone and use whastapp
Exclusion Criteria
Incomplete questionnaires; women with considerable cognitive deficit and with contraindication to breastfeeding.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Result of the use of a multiplatform in the return to the puerperal consultation, data were obtained by tests between groups using the Mann-Whitney test and associations between the categorical variables using the Chi-Square or Fisher's Exact test. During a period of 45 days the intervention took place once a week and after this time evaluation of the participants' return as puerperal consultations
- Secondary Outcome Measures
Name Time Method Result of the use of a multiplatform to control the use of contraceptives after delivery. Data were evaluated by tests between groups using the Mann-Whitney test and associations between categorical variables using the Chi-Square or Fisher's Exact test. ;Breastfeeding rate in the 45-day postpartum period Data were evaluated by tests between groups using the Mann-Whitney test and associations between categorical variables using the Chi-Square or Fisher's Exact test.;Assessment of pregnancy planning and intention. Data were evaluated by tests between groups using the Mann-Whitney test and associations between categorical variables using the Chi-Square or Fisher's Exact test.