Mastodynia
Conditions
Interventions
The study began recruitment on August 23, 2023. The last participating woman was selected on December 15, 2023, however data collection continues and is expected to end on January 15, 2024, with the v
E02.594.540
E02.190.044
Sponsors
Universidade Federal da Paraíba - Programa de Pós-graduação em Saúde Coletiva
Instituto Candida Vargas
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Women with breast pain. Older than 18 years. In Exclusive Breastfeeding (EBF) or mixed. Express a desire to continue breastfeeding. Being in rooming-in with babies born at term (over 37 weeks). Breastfeeding within one month of postpartum
Exclusion criteria
Exclusion criteria: Prolonged hospitalization of the mother or baby. Low birth weight or premature baby. Contraindication to breastfeeding. She has already stopped breastfeeding. Woman with previous mammoplasty. Woman with breast implants. Babies with facial malformations (cleft lip and cleft palate)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to evaluate whether the application of laser therapy and laser acupuncture is related to the difference in the reduction in the average breast pain in the intervention group through the application of the Visual Analogue Scale for pain, before and after conventional treatment or the association of conventional treatment with laser therapy. and laser acupuncture | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the maintenance of exclusive or mixed breastfeeding, it is expected to find out whether there is a greater number of women who maintain exclusive and/or mixed breastfeeding in the intervention group after 15 days and 30 days after birth through a structured multiple questionnaire. choose considering a significance of 0.05;To evaluate the improvement in satisfaction and tranquility in breastfeeding, we hope to find out whether there is an improvement in the average satisfaction and tranquility in the control and intervention groups using a 5-point Likert scale, after 15 days and 30 days after birth using a structured multiple choice questionnaire considering a significance of 0.05 | — |
Countries
Brazil
Contacts
Public ContactDaniela Lima
Centro de Ciências da Saúde da Universidade Federal da Paraíba - CCS/UFPB
Outcome results
None listed