Sleep Disorders of Circadian Rhythm
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Postpartum women: more than 18 years of age; having given birth to an only child; living together for at least 24 hours; being literate; not working at night in the last 3 years; not using illicit drugs during pregnancy; agreeing and signing the free and informed consent term. Newborns: born of any type of birth; full term; by gestational age (DUM); chronological age greater than or equal to 24 hours; birth weight over 2000 grams; no malformations; female or male; and those who are mothers to agree and sign the informed consent form for participation of the neonate in the study.
Exclusion criteria
Exclusion criteria: Postpartum women who present any type of complication after delivery; newborn in phototherapy; with malformation; or postpartum women whose neonate is transferred to another unit.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increase of approximately 10% of the total postpartum women sleep time expressed in minutes and measured by acrometer in 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| Increased levels of 6-sulfatoximelatonin in the postpartum women urine, expressed as ng/mL and identified by the Elisa Method in a research laboratory. 6-Sulfatoxymelatonin will be measured as data collection is obtained. | — |
Countries
Brazil
Contacts
Escola Paulista de Enfermagem da Universidade Federal de São Paulo