Empowering Mothers in the NICU
Empowering Mothers With Hospitalized Infants in the Neonatal Intensive Care Unit Through Integrated Care: A Randomized Controlled Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
Family Integrated Care is designed to eliminate the barriers between parents and their infants in the NICU by involving parents of premature infants in their care. Parents are integrated into both the healthcare team and the care of their infant. Through this approach, parents are informed about how they can contribute to their infant's overall development, including neurological and sensory development, motor and behavioral progress, as well as practices such as touch, bonding, skin-to-skin contact, breastfeeding, and increasing breast milk production. They are also educated on general hygiene and care tasks such as diaper changing and body cleaning. This model places importance on the protection and enhancement of both the physical and psychological well-being of the parent and the infant. During this process, parents move beyond being mere "visitors" in the unit to becoming active "participants" and members of the care team. Family integrated care aims to support parents in becoming the primary caregivers for their infants, both during hospitalization and after discharge. This model not only provides education and counseling but also supports the family's comprehensive involvement in the infant's care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 18, 2025
CompletedFirst Posted
Study publicly available on registry
May 6, 2025
CompletedStudy Start
First participant enrolled
August 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedFebruary 18, 2026
February 1, 2026
4 months
April 18, 2025
February 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Parental Stress in the Neonatal Intensive Care Unit
The Parental Stressor Scale: Neonatal Intensive Care Unit (PSS:NICU) will be used to assess the level of parental perception of stressors arising from the physical and psychosocial environment of the intensive care unit. The scale consists of 34 items across three dimensions: Sights and Sounds, Infant Appearance and Behavior, and Parental Role Alteration. Higher scores on the scale indicate higher levels of parental stress (minimum: 0, maximum: 170).
The mother will be asked to complete the scale form within the first 72 hours of admission to the unit, one day before discharge, and one week after discharge.
Maternal Attachment
The Maternal Attachment Scale consists of 26 items. The total score can range from 26 to 104. A higher score indicates a higher level of maternal attachment.
The mother will be asked to complete the scale form within the first 72 hours of admission to the unit, one day before discharge, and one week after discharge.
Study Arms (2)
Mother Integrated Care Group
EXPERIMENTALMothers whose infants are admitted to the NICU will be contacted within the first 72 hours. Pre-test data (Information Form, Maternal Attachment Scale, and Parental Stressor Scale: Neonatal Intensive Care Unit) will be collected, and education will be planned through a face-to-face interview. After meeting with the mother and administering the pre-test, the training date will be scheduled together with the researchers. The training, which consists of four steps, is planned to be conducted with a two-day interval between each session. The practices will be demonstrated on mannequins and supported by a PowerPoint presentation and visual materials. A booklet prepared specifically for the mothers will also be distributed. After the training steps are completed, mothers will be encouraged to participate in their infant's care in cooperation with the NICU team. One day before discharge and one week after discharge, questionnaire forms will be administered via WhatsApp.
Control group
NO INTERVENTIONMothers in this group will receive standard unit care and education. Data collection procedures will be the same as those used in the intervention group. The mother will be contacted within the first 72 hours of admission to the unit, and pre-test data will be collected. One day before discharge and one week after discharge, questionnaire forms will be administered via WhatsApp.
Interventions
In order to empower mothers whose premature infants have been hospitalized in the neonatal intensive care unit (NICU) for at least three days, a four-step neonatal care training program will be provided. Through the empowerment of the mother, the empowerment of the family will also be supported. The family will no longer be considered as visitors but will be involved in the infant's care in the NICU as parents. Data collection forms will be completed before the training begins, one day prior to discharge, and one week after discharge.
Eligibility Criteria
You may qualify if:
- The newborn must be premature (gestational age \>28 and \<34 weeks),
- The infant must be admitted to the NICU and hospitalized for at least 3 days,
- The mother must be open to communication and cooperation,
- The mother must voluntarily agree to participate in the study,
- The mother must be literate,
- The mother must be able to speak and understand Turkish,
- The mother must be primiparous and experiencing motherhood for the first time,
- The mother must be over 18 years of age,
- Mothers in the intervention group must be present in the hospital for an average of 6-8 hours per day.
You may not qualify if:
- The newborn has a congenital anomaly (e.g., craniofacial anomalies such as cleft palate, cleft lip, or facial muscle paralysis),
- The newborn has a diagnosed gastrointestinal, neurological, or genetic disorder (e.g., necrotizing enterocolitis, hydrocephalus, Down syndrome, omphalocele, gastroschisis, short bowel syndrome, or other diseases),
- The newborn has a congenital heart defect requiring surgical intervention,
- The mother has a diagnosed psychiatric illness,
- The mother and/or father do not wish to participate in the study.
- Withdrawal Criteria:
- The mother does not attend the training sessions during the study period,
- The mother fails to maintain cooperation throughout the study,
- The newborn is transferred to another healthcare center for any reason,
- The mother wishes to withdraw from the study,
- The newborn is diagnosed with a chronic illness during the study process.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Yalova University
Yalova, 77200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
EMEL AVÇİN, Doctor
Adiyaman University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer Dr
Study Record Dates
First Submitted
April 18, 2025
First Posted
May 6, 2025
Study Start
August 30, 2025
Primary Completion
December 30, 2025
Study Completion
February 1, 2026
Last Updated
February 18, 2026
Record last verified: 2026-02