Mothers of newborn infants before the time or in the right time hospitalized in neonatal ICU, under the use of natural intervention based on flowers: clinical research where neither the researcher nor the participant nor the statistician knows which group they belong to and the groups are made by lot

Not Applicable

Recruiting

• Conditions: Psychological stress; premature newborn; Postpartum period; F01.145.126.990; M01.060.703.520.520; G08.686.702

• Registration Number: RBR-7jtmpc
• Lead Sponsor: niversidade Federal de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-10
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Puerperas older or younger than 18 years old with free and informed consent, for adults and or parents and guardians, and Term of Assent, for minors, with no age limit, single-gestation, whose premature born less than 37 weeks old, who are hospitalized at the Neonatal or Semi-Intensive Care Unit for at least 48 hours, who have visited the child at least once, do not present a contraindication to breastfeeding, and have started the expression of the milk in the first 24 hours of hospitalization, which exhibit some level of stress measured from the Parental Stress Scale: Neonatal Intensive Care Unit

Exclusion Criteria

Mothers of newborns who are breastfeeding directly in the mother, puerperal women using galactagogues and or anxiolytics and antidepressants, with mammary malformation or reduction or mammoplasty; foreigners, due to the difficulty of communication and cultural difference, drug users, who do not have a mobile phone.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome variable<br><br>Stress: It refers to the level of stress of the puerperas that will be evaluated in two ways: by the Parental Stress Scale: Neonatal Intensive Care Unit and by the hormonal dosage of cortisol<br><br>There is no cut-off point (score) and the analysis will be done in terms of average because the objective will be to evaluate the reduction or not of the level of stress with the use of the Florals.

Secondary Outcome Measures

Name	Time	Method
Secondary outcome variable<br><br>Milk production: it will be analyzed by means of the volume of milk collected, obtained means of consulting the donor's file. The average volume obtained in the interval of 5 days, between the 7th. and 8th. day and between the 12th. and 13th day after delivery, after the second and third intervention. It is expected an increase of at least 10% increase in dairy production from the beginning to the end of the research for each woman.