- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05005988
Actions for Empowered Maternal Neonatal Care (ACUNE): A Nursing Intervention (ACUNE)
Actions for Empowered Maternal Neonatal Care (ACUNE): Nursing Intervention to Strengthen Mothers' Competence to Care for Their Preterm Infants at Home. A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Premature children have a higher risk of becoming ill and dying than full-term children and that risk do not end with hospitalization, so the care they receive at home is decisive in their health and wellbeing. Preterm infants are especially vulnerable and have a greater number of readmissions and emergency visits after discharge, as well as delays in vaccination, infections as well as nutritional alterations.
Women play central in family health, and it is necessary to design and applying interventions to facilitate a woman's empowerment, specially to care premature son at home after Neonatal Intensive Care Units (NICU) discharge. Preparation for discharge has been described in the literature as a process where the mothers develop skills and knowledge that they will need to care for their premature children once they are at home. However, for mothers, they face a challenging task in which they experience high levels of stress, fear and uncertainty. Premature children require particular care and the mothers need more than knowledge and skills, they also need to get confidence, believe in their abilities and empowerment themselves to participate more actively and safely in decisions that have to do with the health of their children. This study arises from the need to prepare mothers through the possibilities of empowerment, as a way to improve the health outcomes of premature children. A Randomized Clinical Trial is proposed to establish the effect of the educational intervention of empowerment on mothers' competence in premature infant care, readmissions, weight gain, exclusive breastfeeding and other aspects related to the health, survival and well-being of premature infants. The intervention was designed by integrating the theoretical approach, empirical evidence and the results of a qualitative study in which mothers and fathers of premature infants participated, which gives a participatory approach to the research and makes it close to the parents' reality and gives it social relevance.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Sandra P Osorio Galeano, MD
- Phone Number: (57)3004559227
- Email: sandra.osorio@udea.edu.co
Study Contact Backup
- Name: Angela M Salazar Maya, PhD
- Phone Number: (57)3113214501
- Email: angela.salazar@udea.edu.co
Study Locations
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Antioquia
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Medellín, Antioquia, Colombia, 050001
- Recruiting
- Sandra Osorio
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Contact:
- Angela M Salazar Maya, PhD
- Phone Number: (57)3113214501
- Email: angela.salazar@udea.edu.co
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Contact:
- Sandra P Osorio Galeano, Master
- Phone Number: (57)3004559227
- Email: sandra.osorio@udea.edu.co
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Sub-Investigator:
- Angela M Salazar Maya, PhD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Mothers of premature infants less than 37 weeks gestational age at birth.
- Mothers of premature infants hospitalized in the neonatal intensive care unit
Exclusion Criteria:
- Mothers with previous experience in caring for a premature infant.
- Mothers whose children have some type of congenital malformation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Empowerment educational intervention
Three 30-minute sessions will be conducted with each mother in the intervention group, the first during the first week after admission, the second session within 7 days after the second session, and the third 3 to 2 days before discharge.
An induction to the out-of-hospital kangaroo program will also take place on the day of admission to the program.
Mothers will receive a booklet with general care contents and empowerment information.
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The intervention includes three 30-minute face-to-face sessions: Session 1. Recognizing prematurity and the NICU environment: includes definitions of prematurity, characteristics of premature infants, equipment and dynamics of NICU care. Mothers are encouraged to identify their own and contextual resources that can help empower them. Session 2. Identifying the care of a premature baby: aspects related to the kangaroo method, feeding, thermoregulation, among others, are presented. Knowledge is presented as an empowerment resource. Session 3: Preparation for the return home. Aspects related to the discharge process and transition to home are described. Includes information on the transition home, warning signs, emergency situations, physical burden, and recognition of sources of personal and professional support. Session on admission to the out-of-hospital kangaroo program: presents the dynamics of the kangaroo program, as well as the goals in the new care setting.
Other Names:
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No Intervention: Usual intervention
Mothers receive information for home infant care, no theoretical perspective and no empowerment approach is considered
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in the caregiver's competence
Time Frame: At admission (baseline), through hospitalization completion, an average of 3 week and one week after the discharge.
|
The caregiver's competence is the capacity, ability and preparation that the caregiver has to perform his or her caregiving task at home and can be measured with the CUIDAR scale, which was designed and validated in Colombia.
This scale has been used in several studies, confirming its validity and reliability.
To determine the validity and reliability of the CUIDAR instrument in mothers of premature infants, a cross-sectional quantitative study was carried out in which its psychometric properties were measured.
207 mothers of premature infants participated.
A factor analysis did not confirm the original structure in the new population, but a model with 7 factors and 33 items with a Cronbach's alpha of 0.852 and adequate goodness-of-fit indices.
The new version of the scale, named CUIDAR-PreMa, has 7 dimensions: Acting, Coping, Bonding, Social Support, General Knowledge, Singularity and Specific Knowledge.
The scale has 33 items, with a Likert-type scale
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At admission (baseline), through hospitalization completion, an average of 3 week and one week after the discharge.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in premature infant body weight
Time Frame: At admission (baseline), through hospitalization completion, an average of 3 week and one week after the discharge.
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Weight of the premature infant in grams.
Measurements obtained by the percentile curve are evaluated.
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At admission (baseline), through hospitalization completion, an average of 3 week and one week after the discharge.
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Readmission
Time Frame: One week after the discharge
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Readmission iin the week following hospital discharge
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One week after the discharge
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Emergency visits
Time Frame: One week after discharge
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Emergency visits number in the firts week after discharge
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One week after discharge
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Exclusive breastfeeding
Time Frame: One week after discharge
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Exclusive breastfeeding refers to whether the mother covers all of her child's feeding needs with breast milk.
To establish this, a questionnaire will be used to determine how many times a day she expresses breast milk and how many cubic centimeters of breast milk she expresses, whether the premature child has a good suckling ability and whether she has had to give her child formula milk to supplement his or her diet.
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One week after discharge
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sandra P Osorio Galeano, MD, Universidad de Antioquia
- Study Director: Angela M Salazar Maya, PhD, Universidad de Antioquia
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CEI-FE2020-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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