Family Centered CareNCT04761419
Family Centered Care Cohort Study 1 in Nagano Children's Hospital
An observational study of Family Centered Care, run by Nagano Children's Hospital at 1 site in Japan.
Trial summary
An observational cohort study to show the effect of parents' presence beside their infants, skin-to-skin contact (SCC), participation in infant care, or any interaction with their infants on parents' and infants' short- and long-term outcomes. Read more about this study
- Who is it for?
- Ages Up to 7 days
- Conditions the study is for
- Family Centered Care
- What is being tested?
- Parents' longer presence beside their infant
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 90 participants
- Where
- 1 siteJapan
- Study dates
- 1 Feb 2021to Nov 2027
- How long will I take part?
- 3 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 7 days
- All sexes
- No healthy volunteers
- Child
Study population: A level IV NICU in Japan
Who may be able to join
- Born at 34 weeks of gestation or earlier in Nagano Children's Hospital and need admission into NICU in the same hospital
Who cannot join
- Having any major anomalies including suspicion of chromosomal disorder on admission
- At least one parent is Not Japanese
- The consent is not obtained by day 7
- Do not survive until discharge home
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effect of Parents' Presence in Nagano Children's Hospital NICU on Infant and Parent Outcomes
An observational cohort study to show the effect of parents' presence beside their infants, skin-to-skin contact (SCC), participation in infant care, or any interaction with their infants on parents' and infants' short- and long-term outcomes. Investigators create a hypothesis that longer parents' presence, SCC, participation in infant care, and any interaction with their infants affect outcomes of infants and parents by preventing parents' depression and promoting parent-infant bonding and, in addition, by shortening the length of stay, promoting growth, promoting establishment breastfeeding, and improving developmental outcomes. Parents are asked to make a record of the length of their presence, SCC, participation in infant care, and any interaction with their infants, which are quantitative measurements of family centered care (FCC). Investigators also collect the data related to the background information of the family, delivery, the clinical course of infants, and the outcome measures of the infants and parents. No intervention is included in this research.
The study setting is a level IV neonatal intensive care unit (NICU) at Nagano Children's Hospital in Nagano, Japan. Eligible infants are those who are born at 34 weeks of gestation or earlier from Japanese parents in Nagano Children's Hospital and need admission into NICU in the same hospital. Infants are excluded from this study if they have any major anomalies including suspicion of chromosomal disorder on admission, if at least one parent is Not Japanese, or if they do not survive until discharge home.
The primary outcomes are the EPDS and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) of the parents. The secondary outcomes are the followings; (1) length of stay (days), (2) physical measurements at 36 weeks (g or cm) and growth rate from birth to discharge home (g or cm /d), (3) breastmilk-feeding (exclusive, partial, or no breast milk) and the frequency of breastfeeding directly from breast at 36 weeks PMA and at discharge (average frequency per day), and for the infants whose birth weight <1500g only, (4) developmental quotient (DQ) at 6 and 18 months of corrected age, and 3 years old assessed by Kyoto Scale of Psychological Development (KSPD).
Read the detailed description
<Ethical considerations> This research protocol was approved by the Ethics Committee of Nagano Children's Hospital before this research is being conducted. Recruitment is undertaken by the neonatologists in the unit. They provide written and oral information about the study when they explain infants' condition to their parents at admission. The parents are given sufficient time to consider their participation. The informed consent will be asked within 7 days from the birth, otherwise the infant will be excluded from this study. At least one of the parents should sign the informed consent before enrolment. At the time of agreement, investigators give the infant an anonymous number to protect personal information.
< Power calculation > The sample size should be decided by the number of parents as the primary outcomes are for parents. Investigators plan to include 110 couples or families; the power calculation showed that investigators could detect a 2.5 difference in the mean Edinburgh Postnatal Depression Scale (EPDS) score of longer and shorter presence groups (with power 0.8 and alfa 0.05) with this number of parents.
<Measures and data collection> Diary record Parents make a record on daily diary from the next day of agreement to one day before discharge. Parents make a record about duration of these four topics; presence, skin-to-skin contact (SCC), participation in infant care, and any other interaction with their infants.
- "Care taking" includes the followings; breast feeding, bottle feeding, milking, tube feeding, changing diaper, wiping body, bathing, and any other essential care for baby. However, any care taking during "SCC" mustn't included in this section.
- "Other interaction with baby" includes the followings; hugging, holding, touching, watching, talking, reading books, playing, making something or writing diary for baby, and any other approaches for baby. However, any interaction given during "SCC" or "care taking" mustn't included in this section.
Investigators use the modified Parent-Infant Closeness Diary. The original diary includes three items for each mother and father; presence, holding and SCC. Investigators have changed these items into our own settings as above and changed the used language into Japanese. Investigators already have got the permission from the developers of this diary. This diary has one day per page including all the four topics for both parents. Mother and father respectively draw a line on the blank of specific items they do. They should fill all the corresponding blanks when they do things for multiple babies. The start and the end times should be put in 5-minute increments. The validity of Parent-Infant Closeness Diary has already been proven.
Perinatal Data Collection Perinatal information of the infant includes sex, gestational age, birth weight, height, head circumference, mode of delivery, parity and plurality of mother, and Apgar score at 1, 5, and 10 minutes. Investigators will also find out if the infant meets the criteria for small for gestational age (SGA), which is defined as both birth weight and height are <10th percentile.
Perinatal information of the family members includes the first meeting days with the infant and the first SCC days, for mother and father respectively.
Background information of the family includes family composition, presence of mother's supporter, the number of siblings living with parents, and required time from home to the hospital.
Background information of the parents includes the age, the educational background, the smoking history at pregnant, occupation and parental leave, history of depression or any other mental health problem before and during pregnancy and the history of medication for that disease, and the degree of social support, which is measured by the Multidimensional Scale of Perceived Social Support (MSPSS) as mentioned below. These are risk factors of postpartum depression.
Short version of Multidimensional Scale of Perceived Social Support in Japanese (MSPSS-Js) The Multidimensional Scale of Perceived Social Support (MSPSS) is widely used self-report measure of subjectively assessed social support. There have been several modifications for MSPSS and now it consists of 12 questions with 7-point rating scale ranging from very strongly disagree (1) to very strongly agree (7) for each question. There is Japanese version of MSPSS (MSPSS-J), whose reliability and validity have proven. Investigators use short version of MSPSS-J (MSPSS-Js), which consists of only 7 questions with 7-point rating scale ranging from 1 to 7 and has high correlation with full version. The total score varies from minimum 7 to maximum 49, and higher scores indicates to have better social support.
Data Collection of the clinical course The information of the clinical course includes days of invasive ventilation, days of non-invasive ventilation, days of any respiratory support including oxygen, the history of patent ductus arteriosus (PDA) operation, the history of surgical treatment of abdomen, age of full feeding (the amount of enteral nutrition >=100ml/kg/day), the history and the degree of intraventricular hemorrhage (IVH), and the history of retinopathy of prematurity (ROP) treatment.
Evaluation at 36 weeks postmenstrual age (PMA) and discharge Investigators measure the weight (g), height (cm), head circumference(cm), the frequency of breast feeding (per day), and the type of nutrition (exclusive, partial, or no breast milk) at 36 weeks PMA and when the infant discharges home or leaves our NICU to another hospital or ward to prepare for discharge. Investigators also calculate the length of hospital stay (days) and the growth rate of physical measurements between the time of admission and discharge. If the infant leaves our NICU before 36 weeks PMA, investigators use the data at that point as an evaluation at 36 weeks PMA.
The Edinburgh Postnatal Depression Scale (EPDS) and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother and father All mothers and fathers of the infants enrolled in this research undergo the Edinburgh Postnatal Depression Scale (EPDS) and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) at least twice. Almost all mothers who deliver in Nagano Children's Hospital usually undergo the EPDS and MIBS-J at 2 and 4 weeks postpartum at the maternity outpatient clinic. Investigators additionally carry out the EPDS and MIBS-J for fathers in NICU once within a month postpartum, and for both fathers and mothers at discharge of their infant for the purpose of this research.
The EPDS is a screening method for mothers to detect postpartum depressive symptoms. It comprises 10 self-report items, each of which is scored on a four-point scale (0-3). The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms. Investigators use Japanese version of the EPDS, whose reliability and validity have already proven. The cutoff score for Japanese people to indicate probable major postpartum depression should be eight and nine, which is lower than that usually used in western countries.
Mother-to-Infant Bonding Scale (MIBS) is an assessment method for the feelings of a mother towards her new infant, but investigators use Japanese version of MIBS (MIBS-J), whose reliability and validity have already proven. MIBS comprises eight self-report items, but MIBS-J have ten self-report items, each of which is scored on a four-point scale (0-3). The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
The main risk factors of mothers' postpartum depression are prenatal depression and anxiety, previous depression or other mental problems, lower income and occupational status, multiparity, presence of other children, poor marital relationship or without partner, lack of social support, stressful life events, negative image toward pregnancy, and experiences of early mother-infant separation. In addition, the risk factors vary depending on when to evaluate postpartum depression. The depression scores in mothers and fathers of preterm infants is at its highest just after delivery and will reduce over time, which shows different change compared with term birth. This is why investigators have to adjust these confounding factors when investigators evaluate the EPDS and MIBS-J of the parents.
Long-term developmental assessment after discharge (birth weight <1500g) The development of the infants whose birth weight <1500g are assessed by Kyoto Scale of Psychological Development (KSPD) at 6 and 18 months of corrected age, and 3 years old at the outpatient clinic of Nagano Children's Hospital. KSPD is one of the assessment methods to evaluate developmental quotient and it is known to be well correlated with Bayley III. KSPD consists of three subscales: Cognitive-Adaptive, Language-Social, and Postural-Motor.
<Outcomes> The primary outcomes are the EPDS and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) of the parents. Investigators hypothesize that longer parents' presence decreases the EPDS score and MIBS-J score. Investigators will divide mothers and fathers into two groups respectively (longer and shorter presence groups) based on the distribution of the time of parents' presence, and compare the difference of the mean EPDS score and MIBS-J score between these two groups at each point in time measured.
The secondary outcomes are the followings; (1) length of stay (days), (2) physical measurements at 36 weeks (g or cm) and growth rate from birth to discharge home (g or cm /d), (3) breastmilk-feeding (exclusive, partial, or no breast milk) and the frequency of breastfeeding directly from breast at 36 weeks PMA and at discharge (average frequency per day), and for the infants whose birth weight <1500g only, (4) developmental quotient (DQ) at 6 and 18 months of corrected age, and 3 years old assessed by KSPD. Investigators hypothesize that longer parents' presence, SCC, participation in infant care, or any interaction with infant improve these outcomes. Investigators will divide mothers and fathers into two groups respectively (longer and shorter presence groups, SCC, participation in infant care, or any interaction with infant) as mentioned above and compare the difference of these outcomes between these two groups. In addition, investigators also correct the data from the diary as the followings; presence of at least one of their parents, SCC with at least one of their parents, participation of at least one of their parents in infant care, and any interaction with at least one of their parents, and consider the outcomes in the same manner. Investigators will also consider (5) the difference of the mean EPDS score and MIBS-J score between longer and shorter SCC, participation in infant care, or any interaction with infant groups.
<Statistical analysis> As a statistical analysis, investigators will use a mixed effect model for the EPDS score and MIBS-J score, a linear regression model for other continuous variables (length of stay, physical measurements, growth rate, the frequency of breastfeeding and DQ), and a logistic regression model for binary variable (type of nutrition). Potential confounders will be adjusted.
- Conditions
- Family Centered Care
- Being tested
- Parents' longer presence beside their infant
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Parents' longer presence beside their infantBehavioural
Also called Parents' longer skin-to-skin contact, Parents' longer participation in infant care, Parents' longer interaction with their infant
They are not intervention. We will collect data about these items.
What is being measured
The primary outcome is the main question the study is designed to answer.
The Edinburgh Postnatal Depression Scale (EPDS) of mother 1
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Measured: 2 weeks postpartum.
The Edinburgh Postnatal Depression Scale (EPDS) of mother 2
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Measured: 4 weeks postpartum.
The Edinburgh Postnatal Depression Scale (EPDS) of mother 3
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Measured: At discharge of the infant, an average of 2 months postpartum.
The Edinburgh Postnatal Depression Scale (EPDS) of father 1
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Measured: Within 1 month postpartum.
The Edinburgh Postnatal Depression Scale (EPDS) of father 2
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Measured: At discharge of the infant, an average of 2 months postpartum.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 1
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Measured: 2 weeks postpartum.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 2
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Measured: 4 weeks postpartum.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 3
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Measured: At discharge of the infant, an average of 2 months postpartum.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for father 1
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Measured: Within 1 month postpartum.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for father 2
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Measured: At discharge of the infant, an average of 2 months postpartum.
Secondary outcomes (14)
Length of stay
Hospitalization of the infant in NICU
Measured: At discharge of the infant, an average of 2 months postpartum.
Weight at 36 weeks
Weight in grams.
Measured: 36 weeks of postmenstrual age.
Height at 36 weeks
Height in centimeters.
Measured: 36 weeks of postmenstrual age.
Head circumference at 36 weeks
Head circumference in centimeters.
Measured: 36 weeks of postmenstrual age.
Growth rate of weight from birth to discharge home (change)
Weight in grams per day
Measured: At birth and discharge, an average of 2 months postpartum.
Growth rate of height from birth to discharge home (change)
Height in centimeters per day
Measured: At birth and discharge, an average of 2 months postpartum.
Growth rate of head circumference from birth to discharge home (change)
Head circumference in centimeters per day
Measured: At birth and discharge, an average of 2 months postpartum.
Breastmilk-feeding at 36 weeks
Exclusive, partial, or no breast milk
Measured: 36 weeks of postmenstrual age.
Breastmilk-feeding at discharge
Exclusive, partial, or no breast milk
Measured: At discharge, an average of 2 months postpartum.
Frequency of breastfeeding directly from breast at 36 weeks
Average frequency per day
Measured: 36 weeks of postmenstrual age.
Frequency of breastfeeding directly from breast at discharge
Average frequency per day
Measured: At discharge, an average of 2 months postpartum.
Developmental quotient (DQ) at 6 months of corrected age
Assessed by Kyoto Scale of Psychological Development (KSPD), which is calculated by dividing the age of the group into which test scores place the child by the child's corrected age and multiplying by 100. Higher score indicates better development.
Measured: At 6 months of corrected age.
Developmental quotient (DQ) at 18 months of corrected age
Assessed by Kyoto Scale of Psychological Development (KSPD), which is calculated by dividing the age of the group into which test scores place the child by the child's corrected age and multiplying by 100. Higher score indicates better development.
Measured: At 18 months of corrected age.
Developmental quotient (DQ) at 3 years old
Assessed by Kyoto Scale of Psychological Development (KSPD), which is calculated by dividing the age of the group into which test scores place the child by the child's real age and multiplying by 100. Higher score indicates better development.
Measured: 3 years old (3 years of postmenstrual age)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Feb 2021
- Study start1 Feb 2021
- Primary completion16 Mar 2024
- Study completionNov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Family Centered CareStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 90 participants (actual)
- Target duration
- 3 Years
Sponsor and investigators
- Lead sponsor
- Nagano Children's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Ryo Itoshima, MD, Principal investigator, Nagano Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04761419
- Sponsor's protocol ID
- FCC-cohort1
- Status last verified
- Apr 2026
- First submitted
- 12 Feb 2021
- Last updated
- 13 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Parents' Presence in Nagano Children's Hospital NICU on Infant and Parent Outcomes
- ClinicalTrials.gov ID
- NCT04761419
- Acronym / sponsor ID
- FCC-cohort1
- Conditions
- Family Centered Care
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 90 participants (actual)
- Lead sponsor
- Nagano Children's HospitalUniversity, hospital or other
- Study start
- 1 Feb 2021 (actual)
- Primary completion
- 16 Mar 2024 (actual)
- Study completion
- Nov 2027 (estimated)
- First posted
- 18 Feb 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
An observational cohort study to show the effect of parents' presence beside their infants, skin-to-skin contact (SCC), participation in infant care, or any interaction with their infants on parents' and infants' short- and long-term outcomes. Investigators create a hypothesis that longer parents' presence, SCC, participation in infant care, and any interaction with their infants affect outcomes of infants and parents by preventing parents' depression and promoting parent-infant bonding and, in addition, by shortening the length of stay, promoting growth, promoting establishment breastfeeding, and improving developmental outcomes. Parents are asked to make a record of the length of their presence, SCC, participation in infant care, and any interaction with their infants, which are quantitative measurements of family centered care (FCC). Investigators also collect the data related to the background information of the family, delivery, the clinical course of infants, and the outcome measures of the infants and parents. No intervention is included in this research.
The study setting is a level IV neonatal intensive care unit (NICU) at Nagano Children's Hospital in Nagano, Japan. Eligible infants are those who are born at 34 weeks of gestation or earlier from Japanese parents in Nagano Children's Hospital and need admission into NICU in the same hospital. Infants are excluded from this study if they have any major anomalies including suspicion of chromosomal disorder on admission, if at least one parent is Not Japanese, or if they do not survive until discharge home.
The primary outcomes are the EPDS and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) of the parents. The secondary outcomes are the followings; (1) length of stay (days), (2) physical measurements at 36 weeks (g or cm) and growth rate from birth to discharge home (g or cm /d), (3) breastmilk-feeding (exclusive, partial, or no breast milk) and the frequency of breastfeeding directly from breast at 36 weeks PMA and at discharge (average frequency per day), and for the infants whose birth weight <1500g only, (4) developmental quotient (DQ) at 6 and 18 months of corrected age, and 3 years old assessed by Kyoto Scale of Psychological Development (KSPD).
Detailed description
<Ethical considerations> This research protocol was approved by the Ethics Committee of Nagano Children's Hospital before this research is being conducted. Recruitment is undertaken by the neonatologists in the unit. They provide written and oral information about the study when they explain infants' condition to their parents at admission. The parents are given sufficient time to consider their participation. The informed consent will be asked within 7 days from the birth, otherwise the infant will be excluded from this study. At least one of the parents should sign the informed consent before enrolment. At the time of agreement, investigators give the infant an anonymous number to protect personal information.
< Power calculation > The sample size should be decided by the number of parents as the primary outcomes are for parents. Investigators plan to include 110 couples or families; the power calculation showed that investigators could detect a 2.5 difference in the mean Edinburgh Postnatal Depression Scale (EPDS) score of longer and shorter presence groups (with power 0.8 and alfa 0.05) with this number of parents.
<Measures and data collection> Diary record Parents make a record on daily diary from the next day of agreement to one day before discharge. Parents make a record about duration of these four topics; presence, skin-to-skin contact (SCC), participation in infant care, and any other interaction with their infants.
- "Care taking" includes the followings; breast feeding, bottle feeding, milking, tube feeding, changing diaper, wiping body, bathing, and any other essential care for baby. However, any care taking during "SCC" mustn't included in this section.
- "Other interaction with baby" includes the followings; hugging, holding, touching, watching, talking, reading books, playing, making something or writing diary for baby, and any other approaches for baby. However, any interaction given during "SCC" or "care taking" mustn't included in this section.
Investigators use the modified Parent-Infant Closeness Diary. The original diary includes three items for each mother and father; presence, holding and SCC. Investigators have changed these items into our own settings as above and changed the used language into Japanese. Investigators already have got the permission from the developers of this diary. This diary has one day per page including all the four topics for both parents. Mother and father respectively draw a line on the blank of specific items they do. They should fill all the corresponding blanks when they do things for multiple babies. The start and the end times should be put in 5-minute increments. The validity of Parent-Infant Closeness Diary has already been proven.
Perinatal Data Collection Perinatal information of the infant includes sex, gestational age, birth weight, height, head circumference, mode of delivery, parity and plurality of mother, and Apgar score at 1, 5, and 10 minutes. Investigators will also find out if the infant meets the criteria for small for gestational age (SGA), which is defined as both birth weight and height are <10th percentile.
Perinatal information of the family members includes the first meeting days with the infant and the first SCC days, for mother and father respectively.
Background information of the family includes family composition, presence of mother's supporter, the number of siblings living with parents, and required time from home to the hospital.
Background information of the parents includes the age, the educational background, the smoking history at pregnant, occupation and parental leave, history of depression or any other mental health problem before and during pregnancy and the history of medication for that disease, and the degree of social support, which is measured by the Multidimensional Scale of Perceived Social Support (MSPSS) as mentioned below. These are risk factors of postpartum depression.
Short version of Multidimensional Scale of Perceived Social Support in Japanese (MSPSS-Js) The Multidimensional Scale of Perceived Social Support (MSPSS) is widely used self-report measure of subjectively assessed social support. There have been several modifications for MSPSS and now it consists of 12 questions with 7-point rating scale ranging from very strongly disagree (1) to very strongly agree (7) for each question. There is Japanese version of MSPSS (MSPSS-J), whose reliability and validity have proven. Investigators use short version of MSPSS-J (MSPSS-Js), which consists of only 7 questions with 7-point rating scale ranging from 1 to 7 and has high correlation with full version. The total score varies from minimum 7 to maximum 49, and higher scores indicates to have better social support.
Data Collection of the clinical course The information of the clinical course includes days of invasive ventilation, days of non-invasive ventilation, days of any respiratory support including oxygen, the history of patent ductus arteriosus (PDA) operation, the history of surgical treatment of abdomen, age of full feeding (the amount of enteral nutrition >=100ml/kg/day), the history and the degree of intraventricular hemorrhage (IVH), and the history of retinopathy of prematurity (ROP) treatment.
Evaluation at 36 weeks postmenstrual age (PMA) and discharge Investigators measure the weight (g), height (cm), head circumference(cm), the frequency of breast feeding (per day), and the type of nutrition (exclusive, partial, or no breast milk) at 36 weeks PMA and when the infant discharges home or leaves our NICU to another hospital or ward to prepare for discharge. Investigators also calculate the length of hospital stay (days) and the growth rate of physical measurements between the time of admission and discharge. If the infant leaves our NICU before 36 weeks PMA, investigators use the data at that point as an evaluation at 36 weeks PMA.
The Edinburgh Postnatal Depression Scale (EPDS) and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother and father All mothers and fathers of the infants enrolled in this research undergo the Edinburgh Postnatal Depression Scale (EPDS) and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) at least twice. Almost all mothers who deliver in Nagano Children's Hospital usually undergo the EPDS and MIBS-J at 2 and 4 weeks postpartum at the maternity outpatient clinic. Investigators additionally carry out the EPDS and MIBS-J for fathers in NICU once within a month postpartum, and for both fathers and mothers at discharge of their infant for the purpose of this research.
The EPDS is a screening method for mothers to detect postpartum depressive symptoms. It comprises 10 self-report items, each of which is scored on a four-point scale (0-3). The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms. Investigators use Japanese version of the EPDS, whose reliability and validity have already proven. The cutoff score for Japanese people to indicate probable major postpartum depression should be eight and nine, which is lower than that usually used in western countries.
Mother-to-Infant Bonding Scale (MIBS) is an assessment method for the feelings of a mother towards her new infant, but investigators use Japanese version of MIBS (MIBS-J), whose reliability and validity have already proven. MIBS comprises eight self-report items, but MIBS-J have ten self-report items, each of which is scored on a four-point scale (0-3). The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
The main risk factors of mothers' postpartum depression are prenatal depression and anxiety, previous depression or other mental problems, lower income and occupational status, multiparity, presence of other children, poor marital relationship or without partner, lack of social support, stressful life events, negative image toward pregnancy, and experiences of early mother-infant separation. In addition, the risk factors vary depending on when to evaluate postpartum depression. The depression scores in mothers and fathers of preterm infants is at its highest just after delivery and will reduce over time, which shows different change compared with term birth. This is why investigators have to adjust these confounding factors when investigators evaluate the EPDS and MIBS-J of the parents.
Long-term developmental assessment after discharge (birth weight <1500g) The development of the infants whose birth weight <1500g are assessed by Kyoto Scale of Psychological Development (KSPD) at 6 and 18 months of corrected age, and 3 years old at the outpatient clinic of Nagano Children's Hospital. KSPD is one of the assessment methods to evaluate developmental quotient and it is known to be well correlated with Bayley III. KSPD consists of three subscales: Cognitive-Adaptive, Language-Social, and Postural-Motor.
<Outcomes> The primary outcomes are the EPDS and Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) of the parents. Investigators hypothesize that longer parents' presence decreases the EPDS score and MIBS-J score. Investigators will divide mothers and fathers into two groups respectively (longer and shorter presence groups) based on the distribution of the time of parents' presence, and compare the difference of the mean EPDS score and MIBS-J score between these two groups at each point in time measured.
The secondary outcomes are the followings; (1) length of stay (days), (2) physical measurements at 36 weeks (g or cm) and growth rate from birth to discharge home (g or cm /d), (3) breastmilk-feeding (exclusive, partial, or no breast milk) and the frequency of breastfeeding directly from breast at 36 weeks PMA and at discharge (average frequency per day), and for the infants whose birth weight <1500g only, (4) developmental quotient (DQ) at 6 and 18 months of corrected age, and 3 years old assessed by KSPD. Investigators hypothesize that longer parents' presence, SCC, participation in infant care, or any interaction with infant improve these outcomes. Investigators will divide mothers and fathers into two groups respectively (longer and shorter presence groups, SCC, participation in infant care, or any interaction with infant) as mentioned above and compare the difference of these outcomes between these two groups. In addition, investigators also correct the data from the diary as the followings; presence of at least one of their parents, SCC with at least one of their parents, participation of at least one of their parents in infant care, and any interaction with at least one of their parents, and consider the outcomes in the same manner. Investigators will also consider (5) the difference of the mean EPDS score and MIBS-J score between longer and shorter SCC, participation in infant care, or any interaction with infant groups.
<Statistical analysis> As a statistical analysis, investigators will use a mixed effect model for the EPDS score and MIBS-J score, a linear regression model for other continuous variables (length of stay, physical measurements, growth rate, the frequency of breastfeeding and DQ), and a logistic regression model for binary variable (type of nutrition). Potential confounders will be adjusted.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 3 Years
Who may qualify
- Ages
- Up to 7 days
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
- Study population
- A level IV NICU in Japan
Key inclusion criteria (1 listed)
- Born at 34 weeks of gestation or earlier in Nagano Children's Hospital and need admission into NICU in the same hospital
Key exclusion criteria (4 listed)
- Having any major anomalies including suspicion of chromosomal disorder on admission
- At least one parent is Not Japanese
- The consent is not obtained by day 7
- Do not survive until discharge home
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Parents' longer presence beside their infantAlso: Parents' longer skin-to-skin contact, Parents' longer participation in infant care, Parents' longer interaction with their infantThey are not intervention. We will collect data about these items. | Behavioural | – |
Primary outcome
The Edinburgh Postnatal Depression Scale (EPDS) of mother 1
Time frame: 2 weeks postpartum.
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
The Edinburgh Postnatal Depression Scale (EPDS) of mother 2
Time frame: 4 weeks postpartum.
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
The Edinburgh Postnatal Depression Scale (EPDS) of mother 3
Time frame: At discharge of the infant, an average of 2 months postpartum.
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
The Edinburgh Postnatal Depression Scale (EPDS) of father 1
Time frame: Within 1 month postpartum.
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
The Edinburgh Postnatal Depression Scale (EPDS) of father 2
Time frame: At discharge of the infant, an average of 2 months postpartum.
Indicators to estimate depression in parents. The total score varies from minimum 0 to maximum 30, and higher scores indicates to have more depressive symptoms.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 1
Time frame: 2 weeks postpartum.
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 2
Time frame: 4 weeks postpartum.
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for mother 3
Time frame: At discharge of the infant, an average of 2 months postpartum.
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for father 1
Time frame: Within 1 month postpartum.
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
Japanese version of Mother-to-Infant Bonding Scale (MIBS-J) for father 2
Time frame: At discharge of the infant, an average of 2 months postpartum.
Indicators to estimate bonding between infant and parents. The total score varies from minimum 0 to maximum 30, and higher scores indicate a problematic bonding between a mother and her infant.
14 secondary outcomes
Length of stay
Time frame: At discharge of the infant, an average of 2 months postpartum.
Weight at 36 weeks
Time frame: 36 weeks of postmenstrual age.
Height at 36 weeks
Time frame: 36 weeks of postmenstrual age.
Head circumference at 36 weeks
Time frame: 36 weeks of postmenstrual age.
Growth rate of weight from birth to discharge home (change)
Time frame: At birth and discharge, an average of 2 months postpartum.
Growth rate of height from birth to discharge home (change)
Time frame: At birth and discharge, an average of 2 months postpartum.
Growth rate of head circumference from birth to discharge home (change)
Time frame: At birth and discharge, an average of 2 months postpartum.
Breastmilk-feeding at 36 weeks
Time frame: 36 weeks of postmenstrual age.
Breastmilk-feeding at discharge
Time frame: At discharge, an average of 2 months postpartum.
Frequency of breastfeeding directly from breast at 36 weeks
Time frame: 36 weeks of postmenstrual age.
Frequency of breastfeeding directly from breast at discharge
Time frame: At discharge, an average of 2 months postpartum.
Developmental quotient (DQ) at 6 months of corrected age
Time frame: At 6 months of corrected age.
Developmental quotient (DQ) at 18 months of corrected age
Time frame: At 18 months of corrected age.
Developmental quotient (DQ) at 3 years old
Time frame: 3 years old (3 years of postmenstrual age)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Apr 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ryo Itoshima, MD principal investigator
Nagano Children's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Family Centered Care, run by Nagano Children's Hospital at 1 site in Japan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Japan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The Edinburgh Postnatal Depression Scale (EPDS) of mother 1 (time frame: 2 weeks postpartum.). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.