Complication of Surgical ProcedureNCT02030951
Measurement of Feeding Experience for Infants With Non-Oral Feedings
An observational study of Complication of Surgical Procedure, run by Medical College of Wisconsin at 1 site in United States.
Trial summary
Feeding that circumvents the oral cavity drastically alters the infant's feeding experience (pre, intra and post feeding) and may lead to oral feeding difficulty. It is estimated that 35 - 40% of infants exhibit oral feeding difficulty. Read more about this study
- Who is it for?
- Ages Up to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Complication of Surgical Procedure
- How many people
- 27 participants
- Where
- 1 siteUnited States
- Study dates
- Jan 2014to Aug 2015
- Phase
- Observational
- Are there results?
- None posted in the registry
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 50 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Study population: Seventy-five infants who are expected to receive a minimum of two weeks of non-oral formula/breast milk feedings during hospitalization and their mothers.
Infant Inclusion Criteria: * prior surgical treatment for gut,
- chest surgery (non cardiac),
- or non-surgical infants who will require a minimum of 2 weeks of non-oral formula/breast milk feedings,
- may be receiving oxygen therapy and intravenous therapy.
- may have previously been treated for sepsis, pneumonia, received intravenous only intake, or managed with assisted ventilation. Maternal Inclusion criteria: *must be able to read and comprehend English. Infant Exclusion Criteria: *infant receiving assisted ventilation,
Trial locations and contacts
1 site in 1 country.
United States1 site
Children's Hospital of Wisconsin
Milwaukee, Wisconsin, 53201
About this study
Feeding that circumvents the oral cavity drastically alters the infant's feeding experience (pre, intra and post feeding) and may lead to oral feeding difficulty. It is estimated that 35 - 40% of infants exhibit oral feeding difficulty. Consequences include delayed oral feeding, growth failure, and inadequate mother-infant interaction. Behaviors related to the feeding experience include behavioral state transitions, orally directed behaviors, hunger and satiation cues, and social interactive behaviors. It is unknown whether these early behaviors differ for hospitalized infants who receive long term tube feedings when compared with infants fed orally or whether alterations in these behaviors can be early indicators of later oral feeding difficulty. Documentation of these missing or altered behaviors is needed prior to the development and testing of interventions to prevent oral feeding difficulty.
For 75 hospitalized infants with long term tube feedings, this research will: 1) describe the range of early feeding behaviors encompassing the feeding experience; 2) identify the change in early feeding behaviors throughout hospitalization; 3) compare the early feeding behaviors of infants with and without oral feeding difficulty at 12 months corrected age (CA); and 4) compare parent perception and provider assessment of feeding, for infants with and without oral feeding difficulty.
We will document infant behaviors surrounding the feeding experience during tube feedings weekly during hospital stay. Throughout the first year of life, infant growth, parent perception and clinician assessment of infant feeding and infant and maternal behavior during feeding will be evaluated to document the occurrence of oral feeding difficulty, allowing for a comparison with early in hospital feeding behaviors. To analyze for changes over time, we will use Generalized Linear Mixed Models (GLMM) for repeated count (Poisson) and frequency/categorical (logistic and multinomial logistic) outcomes (e.g., frequency of infant behaviors). Understanding the constellation of these behaviors and when they begin, will guide the development of interventions whose goal will be to alleviate the long term consequences of oral feeding difficulty, inform clinical practice, and reduce cost.
Read the detailed description
SPECIFIC AIMS: Feeding that circumvents the oral cavity drastically alters the infant's feeding experience and may lead to oral feeding difficulty. It is estimated that 35 - 40% of infants exhibit oral feeding difficulty and 34% of infants evaluated for oral feeding difficulty develop oral feeding resistance during the first year of life. Behaviors associated with oral feeding difficulty include: unclear infant behaviors signaling hunger or satiation; the infant frequently interrupts the feeding, spitting or vomiting, or postural changes during the feeding; infant irritability; increased or decreased length of feeding; delayed acquisition of feeding skills, and disengagement during feeding. Oral feeding resistance is more severe and includes persistent food refusal >1 month, disruptive mealtime behavior, rigid food preferences, gagging in anticipation of feeding, and/or vomiting and failure to master feeding skills consistent with the child's developmental level. The consequences of oral feeding difficulty involve: delayed oral feeding, growth failure, delayed perceptual motor performance, and disengagement with the caregiver related to feeding, which leads to less optimal patterns of parent-infant interaction. It is currently unknown what the early indicators of oral feeding difficulty are or when they begin to develop. The purpose of this research is to prospectively describe early feeding and social interactive behaviors of tube fed infants prior to the later development of oral feeding difficulty and retrospectively compare differences in these behaviors in infants who exhibit oral feeding difficulty with infants not exhibiting these behaviors.
Throughout the first year of life, infant growth, parent perception of infant feeding, clinician assessment of infant feeding skills, and infant and maternal behavior during feeding will be evaluated to document the occurrence of oral feeding difficulty, allowing for a comparison of these early in hospital feeding behaviors. The study aims are to:
Aim 1: Describe the range of early feeding behaviors (pre-feeding, intra feeding, and post) and feeding progression in hospitalized infants who have long term exposure to naso-gastric, oral-gastric and gastrostomy tube feedings. Feeding behaviors are measured as behavioral states, orally directed behaviors, social interactive behaviors (engagement and disengagement behaviors), hunger and satiation cues, sucking organization, and motor activity. Feeding progression is measured as the daily change in the proportion of tube to oral intake.
Aim 2: Identify the change in early feeding behaviors throughout the infant's hospital stay.
Aim 3: Compare the early feeding behaviors of infants with and without oral feeding difficulty at 12 months corrected age (CA).
Aim 4: Compare parent perception and provider assessment of feeding, maternal sensitivity to infant, response to distress, social-emotional and cognitive growth foster cues and infant clarity of cues and responsivity to mother during feeding at hospital discharge and 2, 4, 6, and 12 months CA for infants with and without oral feeding difficulty at 12 months CA.
BACKGROUND AND SIGNIFICANCE: While most healthy infants establish the recurring cycle of hunger, oral feeding, and satiation in association with transition of behavioral states, orally directed behaviors, and social interaction, hospitalized infants often experience tube or intravenous feeding for extended periods of time, which contributes to non-establishment of hunger, feeding, and satiation patterns. Unlike normal healthy infants who experience the pleasurable sensations of smell, taste, touch, and social interaction associated with oral feeding, hospitalized infants often have aversive oral experiences related to intubation, insertion of oral gastric tubes, and suctioning. Behaviors associated with oral feeding difficulty include: unclear infant behaviors signaling hunger or satiation; the infant frequently interrupts the feeding, frequent interruptions, spitting or vomiting, or postural changes during the feeding; infant irritability; increased or decreased length of feeding; delayed acquisition of feeding skills, and behavioral disengagement during feeding. Oral feeding resistance is more severe and may include but is not limited to food refusal, disruptive mealtime behavior, rigid food preferences, increased or decreased length of feeding, altered patterns of mother-infant interaction, suboptimal growth, and failure to master feeding skills consistent with the child's developmental level. The consequences include: delayed oral feeding, and disengagement with the caregiver related to feeding (which leads to parent/caregiver frustration.
The cost of tube feeding averages $40,000 during the first year of life. The cost of outpatient behavioral treatment ranges from $10,000 to $52,000 and readmission treatment averages $ 330,000.
Infant Characteristics and Behaviors Related to Feeding and Oral Feeding Difficulty: The feeding experience encompasses the infant's preparation for feeding (prefeeding period), as well as the actual feeding (intra feeding) and post feeding periods. Feeding involves complex anatomic structures, coordination of breathing, sucking and swallowing, reflex activity, a constellation of behaviors, and social interaction. Several infant characteristics including gestational age (GA), post menstrual age, birth weight, health status, and long term tube feeding have been shown to influence oral feeding.
There is a paucity of research that identifies the constellation of behaviors prior to, during and post feeding for infants during tube feedings. Additionally, interventions currently in use for hospitalized infants experiencing feeding difficulties predominately address the intra feeding period. Management of oral feeding difficulty for older infants/children is intensive, yet also addresses the intra feeding period.
Oral Feeding Progression: Low level oral feeding skills and slow feeding progression are key indicators of oral feeding difficulty. Lau and Smith categorized levels of oral feeding skill that include fatigue and endurance. Infants with more alert behavioral states progressed more quickly to complete oral feedings.
Importance of Mother-Infant Interaction: Feeding holds the central opportunity for the development of long lasting patterns of mother infant interaction. Feeding is critically important because it involves mother-infant interaction; is a primary factor that affects growth; and is a major concern for both clinicians and parents during the transition to full oral feeding and through discharge to home. When the infant is unable able to engage with the mother during feedings, this difficulty leads to non-optimal mother-infant interaction and the potential for altered infant development.
Oral Feeding Difficulty: Oral feeding difficulty is identified by both parents and clinicians. Parent perception offers detailed information from the parent's perspective and includes ease/difficulty of feeding the infant, the infant's behavioral cues surrounding the feeding experience, how the parent sets up and begins the feedings, and the length of feeding. Clinician assessment identifies the infant's oral feeding skills.
Design and Methods Prospective design. Infant feeding behavior, feeding progression, and growth will be evaluated weekly during hospital stay. Parent perception and clinician assessment of oral feeding difficulty will be evaluated at 2, 4, 6, and 12 months corrected age. Mother-infant interaction will be evaluated at hospital discharge and throughout the first year of life.
Sample: We will enroll 75 infants from Children's Hospital of Wisconsin (CHW) who are expected to receive a minimum of two weeks of non-oral formula/breast milk feedings during hospitalization. Infants meeting the following criteria will be eligible for this study: prior surgical treatment for gut, or chest surgery (non cardiac), or non-surgical infants who will require a minimum of two weeks of non-oral formula/breast milk feedings. Infants may be receiving oxygen therapy and intravenous therapy. Infants may have previously been treated for sepsis, pneumonia, received intravenous only intake, or managed with assisted ventilation.
Exclusion criteria include those infants who are currently being treated for sepsis, pneumonia, intravenous only intake, receiving assisted ventilation, have congenital anomalies of the oral cavity, chromosomal abnormalities, or are not neurologically intact (e.g. hypoxic ischemic encephalopathy or significant neurologic deficit).
Procedures Procedures for Data Collection. Evaluation data are collected at enrollment, weekly during hospitalization, at hospital discharge, and at 2, 4, 6, and 12 months CA. At enrollment, after informed consent is obtained, the in-hospital research nurse will conduct the medical record review and obtain the infant demographics/risk factors.
The early feeding behaviors data will be obtained weekly. Infants will be video recorded for 90 minutes. The first 30 minutes will comprise the pre feeding time. Immediately following the 30 minute pre feeding recording, the infant will be fed (approximately 20 - 30 minutes for the feeding). After the feeding is complete, the video recording will be continued for an additional 30 minutes. The early feeding behaviors data are assessed during the entire 90 minute data collection session. Infants will remain on their cardiac monitors during the session. The video recorded data will be transferred from the video camera to the secure (encrypted) server and saved. The video recordings will also be downloaded into the Mangold system for coding. The feeding progression data will be collected from the medical record.
Outcomes assessed at hospital discharge. Within 24 hours of discharge, the final assessment of early feeding behaviors will occur. In addition, sucking organization will be measured for infants who are partially or fully oral fed at discharge. The medical record will be reviewed for the hospital progression data (feeding progression, type of feeding the infant receives, weight gain, length, head circumference, length of hospital stay). The oral feeding skills and sucking organization data will be collected by a member of the research team. Mother-infant interaction will be assessed during a feeding.
Outcomes assessed after Infant Discharge at 2, 4, 6, and 12 months CA. Infant growth and mother-Infant interaction during feeding and play will be assessed at 2, 4, 6, and 12 months CA in the Pediatric Translational Research Unit. Difficulty with Oral Feeding during the infant's first 12 months, will be identified through parent self report and clinician assessment. Mother-infant interaction will be assessed during a feeding.
Statistical Analysis Plan: Frequencies and 95% confidence intervals based on the appropriate model for the variation will be calculated for the behavioral data and changes in the behavior over time. The behavioral data will be converted to percents, counts and rates over time (weeks) to evaluate change over time (maturation). Changes over time will be modeled as linear, curvilinear or step functions with fractional polynomials. Analysis of changes over time will use Generalized Linear Mixed Models (GLMM) for repeated count (Poisson) and frequency/categorical (logistic and multinomial logistic). Where the outcome occurs only once, such as feeding by tube at discharge, the corresponding Generalized Linear Model (GLM) will be used for regression modeling; e.g. a Poisson GLM instead of Poisson GLMM, a logistic GLM in place of a logistic GLMM, etc. (AIM 1 and AIM 3).
- Conditions
- Complication of Surgical Procedure
- Keywords
- preterm infant behavior, tube feeding, feeding efficiency
What is being measured
The primary outcome is the main question the study is designed to answer.
Oral Feeding Difficulty
Oral feeding difficulty will be identified through parent self report and clinician assessment at 2,4,6, and 12 months CA.
Measured: 12 months of life
Secondary outcomes (1)
Feeding progression
Ability to feed orally
Measured: over the first year of life
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jan 2014 (estimated)
- Study startJan 2014
- Primary completionAug 2015
- Study completionAug 2015
Why it stopped: Funding completed
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Complication of Surgical ProcedureStudies of the same condition, open and under way.
- More trials run by Medical College of WisconsinThe sponsor's other registered studies.
- 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
- 27 participants (actual)
Sponsor and investigators
- Lead sponsor
- Medical College of Wisconsin
- Sponsor type
- University, hospital or other
- Collaborators
- Children's Hospital and Health System Foundation, Wisconsin
- Responsible party
- Principal investigator, Rosemary White-Traut, Medical College of Wisconsin
- Investigators
- Rosemary C. White-Traut, PhD, Principal investigator, Children's Hospital and Health System Foundation, Wisconsin
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02030951
- Sponsor's protocol ID
- CHW 13/115
- Status last verified
- Jul 2026
- First submitted
- 11 Dec 2013
- Last updated
- 30 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Measurement of Feeding Experience for Infants With Non-Oral Feedings
- ClinicalTrials.gov ID
- NCT02030951
- Acronym / sponsor ID
- CHW 13/115
- Conditions
- Complication of Surgical Procedure
- Keywords
- preterm infant behavior, tube feeding, feeding efficiency
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Funding completed
- Enrolment
- 27 participants (actual)
- Lead sponsor
- Medical College of WisconsinUniversity, hospital or other
- Collaborators
- Children's Hospital and Health System Foundation, Wisconsin
- Study start
- Jan 2014
- Primary completion
- Aug 2015 (actual)
- Study completion
- Aug 2015 (actual)
- First posted
- 9 Jan 2014 (estimated)
- 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.
Feeding that circumvents the oral cavity drastically alters the infant's feeding experience (pre, intra and post feeding) and may lead to oral feeding difficulty. It is estimated that 35 - 40% of infants exhibit oral feeding difficulty. Consequences include delayed oral feeding, growth failure, and inadequate mother-infant interaction. Behaviors related to the feeding experience include behavioral state transitions, orally directed behaviors, hunger and satiation cues, and social interactive behaviors. It is unknown whether these early behaviors differ for hospitalized infants who receive long term tube feedings when compared with infants fed orally or whether alterations in these behaviors can be early indicators of later oral feeding difficulty. Documentation of these missing or altered behaviors is needed prior to the development and testing of interventions to prevent oral feeding difficulty.
For 75 hospitalized infants with long term tube feedings, this research will: 1) describe the range of early feeding behaviors encompassing the feeding experience; 2) identify the change in early feeding behaviors throughout hospitalization; 3) compare the early feeding behaviors of infants with and without oral feeding difficulty at 12 months corrected age (CA); and 4) compare parent perception and provider assessment of feeding, for infants with and without oral feeding difficulty.
We will document infant behaviors surrounding the feeding experience during tube feedings weekly during hospital stay. Throughout the first year of life, infant growth, parent perception and clinician assessment of infant feeding and infant and maternal behavior during feeding will be evaluated to document the occurrence of oral feeding difficulty, allowing for a comparison with early in hospital feeding behaviors. To analyze for changes over time, we will use Generalized Linear Mixed Models (GLMM) for repeated count (Poisson) and frequency/categorical (logistic and multinomial logistic) outcomes (e.g., frequency of infant behaviors). Understanding the constellation of these behaviors and when they begin, will guide the development of interventions whose goal will be to alleviate the long term consequences of oral feeding difficulty, inform clinical practice, and reduce cost.
Detailed description
SPECIFIC AIMS: Feeding that circumvents the oral cavity drastically alters the infant's feeding experience and may lead to oral feeding difficulty. It is estimated that 35 - 40% of infants exhibit oral feeding difficulty and 34% of infants evaluated for oral feeding difficulty develop oral feeding resistance during the first year of life. Behaviors associated with oral feeding difficulty include: unclear infant behaviors signaling hunger or satiation; the infant frequently interrupts the feeding, spitting or vomiting, or postural changes during the feeding; infant irritability; increased or decreased length of feeding; delayed acquisition of feeding skills, and disengagement during feeding. Oral feeding resistance is more severe and includes persistent food refusal >1 month, disruptive mealtime behavior, rigid food preferences, gagging in anticipation of feeding, and/or vomiting and failure to master feeding skills consistent with the child's developmental level. The consequences of oral feeding difficulty involve: delayed oral feeding, growth failure, delayed perceptual motor performance, and disengagement with the caregiver related to feeding, which leads to less optimal patterns of parent-infant interaction. It is currently unknown what the early indicators of oral feeding difficulty are or when they begin to develop. The purpose of this research is to prospectively describe early feeding and social interactive behaviors of tube fed infants prior to the later development of oral feeding difficulty and retrospectively compare differences in these behaviors in infants who exhibit oral feeding difficulty with infants not exhibiting these behaviors.
Throughout the first year of life, infant growth, parent perception of infant feeding, clinician assessment of infant feeding skills, and infant and maternal behavior during feeding will be evaluated to document the occurrence of oral feeding difficulty, allowing for a comparison of these early in hospital feeding behaviors. The study aims are to:
Aim 1: Describe the range of early feeding behaviors (pre-feeding, intra feeding, and post) and feeding progression in hospitalized infants who have long term exposure to naso-gastric, oral-gastric and gastrostomy tube feedings. Feeding behaviors are measured as behavioral states, orally directed behaviors, social interactive behaviors (engagement and disengagement behaviors), hunger and satiation cues, sucking organization, and motor activity. Feeding progression is measured as the daily change in the proportion of tube to oral intake.
Aim 2: Identify the change in early feeding behaviors throughout the infant's hospital stay.
Aim 3: Compare the early feeding behaviors of infants with and without oral feeding difficulty at 12 months corrected age (CA).
Aim 4: Compare parent perception and provider assessment of feeding, maternal sensitivity to infant, response to distress, social-emotional and cognitive growth foster cues and infant clarity of cues and responsivity to mother during feeding at hospital discharge and 2, 4, 6, and 12 months CA for infants with and without oral feeding difficulty at 12 months CA.
BACKGROUND AND SIGNIFICANCE: While most healthy infants establish the recurring cycle of hunger, oral feeding, and satiation in association with transition of behavioral states, orally directed behaviors, and social interaction, hospitalized infants often experience tube or intravenous feeding for extended periods of time, which contributes to non-establishment of hunger, feeding, and satiation patterns. Unlike normal healthy infants who experience the pleasurable sensations of smell, taste, touch, and social interaction associated with oral feeding, hospitalized infants often have aversive oral experiences related to intubation, insertion of oral gastric tubes, and suctioning. Behaviors associated with oral feeding difficulty include: unclear infant behaviors signaling hunger or satiation; the infant frequently interrupts the feeding, frequent interruptions, spitting or vomiting, or postural changes during the feeding; infant irritability; increased or decreased length of feeding; delayed acquisition of feeding skills, and behavioral disengagement during feeding. Oral feeding resistance is more severe and may include but is not limited to food refusal, disruptive mealtime behavior, rigid food preferences, increased or decreased length of feeding, altered patterns of mother-infant interaction, suboptimal growth, and failure to master feeding skills consistent with the child's developmental level. The consequences include: delayed oral feeding, and disengagement with the caregiver related to feeding (which leads to parent/caregiver frustration.
The cost of tube feeding averages $40,000 during the first year of life. The cost of outpatient behavioral treatment ranges from $10,000 to $52,000 and readmission treatment averages $ 330,000.
Infant Characteristics and Behaviors Related to Feeding and Oral Feeding Difficulty: The feeding experience encompasses the infant's preparation for feeding (prefeeding period), as well as the actual feeding (intra feeding) and post feeding periods. Feeding involves complex anatomic structures, coordination of breathing, sucking and swallowing, reflex activity, a constellation of behaviors, and social interaction. Several infant characteristics including gestational age (GA), post menstrual age, birth weight, health status, and long term tube feeding have been shown to influence oral feeding.
There is a paucity of research that identifies the constellation of behaviors prior to, during and post feeding for infants during tube feedings. Additionally, interventions currently in use for hospitalized infants experiencing feeding difficulties predominately address the intra feeding period. Management of oral feeding difficulty for older infants/children is intensive, yet also addresses the intra feeding period.
Oral Feeding Progression: Low level oral feeding skills and slow feeding progression are key indicators of oral feeding difficulty. Lau and Smith categorized levels of oral feeding skill that include fatigue and endurance. Infants with more alert behavioral states progressed more quickly to complete oral feedings.
Importance of Mother-Infant Interaction: Feeding holds the central opportunity for the development of long lasting patterns of mother infant interaction. Feeding is critically important because it involves mother-infant interaction; is a primary factor that affects growth; and is a major concern for both clinicians and parents during the transition to full oral feeding and through discharge to home. When the infant is unable able to engage with the mother during feedings, this difficulty leads to non-optimal mother-infant interaction and the potential for altered infant development.
Oral Feeding Difficulty: Oral feeding difficulty is identified by both parents and clinicians. Parent perception offers detailed information from the parent's perspective and includes ease/difficulty of feeding the infant, the infant's behavioral cues surrounding the feeding experience, how the parent sets up and begins the feedings, and the length of feeding. Clinician assessment identifies the infant's oral feeding skills.
Design and Methods Prospective design. Infant feeding behavior, feeding progression, and growth will be evaluated weekly during hospital stay. Parent perception and clinician assessment of oral feeding difficulty will be evaluated at 2, 4, 6, and 12 months corrected age. Mother-infant interaction will be evaluated at hospital discharge and throughout the first year of life.
Sample: We will enroll 75 infants from Children's Hospital of Wisconsin (CHW) who are expected to receive a minimum of two weeks of non-oral formula/breast milk feedings during hospitalization. Infants meeting the following criteria will be eligible for this study: prior surgical treatment for gut, or chest surgery (non cardiac), or non-surgical infants who will require a minimum of two weeks of non-oral formula/breast milk feedings. Infants may be receiving oxygen therapy and intravenous therapy. Infants may have previously been treated for sepsis, pneumonia, received intravenous only intake, or managed with assisted ventilation.
Exclusion criteria include those infants who are currently being treated for sepsis, pneumonia, intravenous only intake, receiving assisted ventilation, have congenital anomalies of the oral cavity, chromosomal abnormalities, or are not neurologically intact (e.g. hypoxic ischemic encephalopathy or significant neurologic deficit).
Procedures Procedures for Data Collection. Evaluation data are collected at enrollment, weekly during hospitalization, at hospital discharge, and at 2, 4, 6, and 12 months CA. At enrollment, after informed consent is obtained, the in-hospital research nurse will conduct the medical record review and obtain the infant demographics/risk factors.
The early feeding behaviors data will be obtained weekly. Infants will be video recorded for 90 minutes. The first 30 minutes will comprise the pre feeding time. Immediately following the 30 minute pre feeding recording, the infant will be fed (approximately 20 - 30 minutes for the feeding). After the feeding is complete, the video recording will be continued for an additional 30 minutes. The early feeding behaviors data are assessed during the entire 90 minute data collection session. Infants will remain on their cardiac monitors during the session. The video recorded data will be transferred from the video camera to the secure (encrypted) server and saved. The video recordings will also be downloaded into the Mangold system for coding. The feeding progression data will be collected from the medical record.
Outcomes assessed at hospital discharge. Within 24 hours of discharge, the final assessment of early feeding behaviors will occur. In addition, sucking organization will be measured for infants who are partially or fully oral fed at discharge. The medical record will be reviewed for the hospital progression data (feeding progression, type of feeding the infant receives, weight gain, length, head circumference, length of hospital stay). The oral feeding skills and sucking organization data will be collected by a member of the research team. Mother-infant interaction will be assessed during a feeding.
Outcomes assessed after Infant Discharge at 2, 4, 6, and 12 months CA. Infant growth and mother-Infant interaction during feeding and play will be assessed at 2, 4, 6, and 12 months CA in the Pediatric Translational Research Unit. Difficulty with Oral Feeding during the infant's first 12 months, will be identified through parent self report and clinician assessment. Mother-infant interaction will be assessed during a feeding.
Statistical Analysis Plan: Frequencies and 95% confidence intervals based on the appropriate model for the variation will be calculated for the behavioral data and changes in the behavior over time. The behavioral data will be converted to percents, counts and rates over time (weeks) to evaluate change over time (maturation). Changes over time will be modeled as linear, curvilinear or step functions with fractional polynomials. Analysis of changes over time will use Generalized Linear Mixed Models (GLMM) for repeated count (Poisson) and frequency/categorical (logistic and multinomial logistic). Where the outcome occurs only once, such as feeding by tube at discharge, the corresponding Generalized Linear Model (GLM) will be used for regression modeling; e.g. a Poisson GLM instead of Poisson GLMM, a logistic GLM in place of a logistic GLMM, etc. (AIM 1 and AIM 3).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- Up to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
- Study population
- Seventy-five infants who are expected to receive a minimum of two weeks of non-oral formula/breast milk feedings during hospitalization and their mothers.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Oral Feeding Difficulty
Time frame: 12 months of life
Oral feeding difficulty will be identified through parent self report and clinician assessment at 2,4,6, and 12 months CA.
1 secondary outcome
Feeding progression
Time frame: over the first year of life
Results and safety
The study was stopped early (reason given: Funding completed). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jul 2026.
Related trials for Complication of Surgical Procedure
Recruiting
A Study to Compare Two Surgical Procedures in Individuals With BRCA1 Mutations to Assess Reduced Risk of Ovarian Cancer
Ovarian Carcinoma
Recruiting
Prospective, Multicenter, Randomized Controlled Phase III Trial of Biological Mesh for Alimentary Tract Reconstruction in Digestive Surgery
Digestive System Surgical Procedures, Anastomosis, Surgical
RecruitingPhase 3
Lanreotide Versus Placebo Before Surgery to Prevent a Surgical Complication Called a Pancreatic Fistula
Pancreatic Carcinoma, Pancreatic Neoplasm
Recruiting
Efficacy of Ovarian Drilling Via vNOTES Laparoscopy in Patients With PCOS
PCOS (Polycystic Ovary Syndrome)
Recruiting
Safety and Efficacy of NTP in Thyroid Surgery: Pilot Study on Morbidity Prevention and Adjuvant Oncological Control
Thyroid Diseases, Wound Healing
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.
Rosemary C. White-Traut, PhD principal investigator
Children's Hospital and Health System Foundation, Wisconsin
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 Complication of Surgical Procedure, run by Medical College of Wisconsin at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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: stopped early, as of the sponsor's last update on 30 Jul 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 United States. 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?
The study was stopped early (reason given: Funding completed). Results are not available in the source record.
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?
Oral Feeding Difficulty (time frame: 12 months of life). 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 30 Jul 2026.