Responsive Infant FeedingNCT06898190
Testing LEIFc in the Community
A study testing Learning Early Infant Feeding Cues (LEIFc) in people with Responsive Infant Feeding and Infant Growth, run by Florida State University at 1 site in United States.
Trial summary
The reason that we are doing this research is to teach mothers ways to communicate with their baby during feeding. Understanding signals a baby gives helps mothers know when and how much to feed their baby which will help the baby grow in a healthy way. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Responsive Infant Feeding, Infant Growth
- What is being tested?
- Learning Early Infant Feeding Cues (LEIFc)
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 29 participants
- Where
- 1 siteUnited States
- Study dates
- 10 Apr 2022to 31 Oct 2023
- Phase
- Interventional
- 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 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- pregnant in the 3rd trimester (28 weeks or beyond) of a healthy pregnancy
- pregnant with a single fetus
- 18 years or older
- no known complications or genetic anomalies of the infant that would interfere with feeding or growth after birth
- English or Spanish speaking
Who cannot join
- mother less than 18 years
- will not have custody of the infant after birth
Trial locations and contacts
1 site in 1 country.
United States1 site
Florida State University
Tallahassee, Florida, 32306
About this study
Official title: Testing the Feasibility & Fidelity of the Learning Early Infant Feeding Cues (LEIFc) Intervention
The reason that we are doing this research is to teach mothers ways to communicate with their baby during feeding. Understanding signals a baby gives helps mothers know when and how much to feed their baby which will help the baby grow in a healthy way.
There are 5 study visits, 1 during pregnancy and 4 after the baby is born. At the first visit participants will watch some videos about feeding babies and be provided with information to read about feeding babies, there is also a questionnaire to complete. After the baby is born, a research team member will come to participants' homes at infant age of 1, 2, 3, and 4 months to videotape an infant feeding session. At the visit when the baby is 2 and 3 months of age, the intervention will occur in which the interventionists will provide coaching about responsive feeding before and during a feeding session. The baby's height and weight will be collected and some questionnaires completed. At the last study visit, a research assistant will ask opened ended questions about the study itself, these questions and participant answers will be audio recorded.
Read the detailed description
3.0 Background* 3.1 and 3.3 Health disparities in pediatric obesity are staggering; Non-Hispanic black and Hispanic children have obesity rates (22.2% and 25.8% respectively) higher than the national average (18.5%) and higher than non-Hispanic white children (14.1%).1,2 Additionally, children of low socioeconomic status (SES) are more likely to have obesity.2,3 These same populations are disproportionately affected by lifelong cardiometabolic conditions that result from obesity such as hypercholesterolemia, hypertension, and type 2 diabetes.4 Children with obesity are also more likely to suffer from mental health disorders (i.e., depression, anxiety) and complications of the pulmonary, orthopedic, and gastrointestinal systems.2,5,6 Lifestyle modifications implemented early in life are key to preventing obesity and the resulting lifelong complications. The first 1,000 days of life, from conception to age two years, is a critical period for development of habits that contribute to one's weight status later in life, such as dietary preferences and behaviors.7-10 Therefore, interventions implemented during the first 1,000 days and targeting infants from high-risk groups have potential to decrease one's obesity risk and address racial/ethnic and socioeconomic health disparities.
Infant feeding practices, which include what and how infants are fed, are one such habit that could be modified to decrease obesity risk.5 Exclusive formula feeding, short duration of breastfeeding when initiated, and early introduction of complementary foods contribute to rapid infant weight gain which, in turn, contributes to higher risk for childhood obesity.11,12 Many initiatives have targeted "what" infants are fed (i.e., promoting breastfeeding and healthy dietary intake) whereas "how" infants are fed is also important, yet understudied.5,8,13,14 The responsive feeding approach is thought to promote the ability to recognize and respond to internal cues of hunger and satiety.13-17 The ability to recognize these internal cues and self-regulate intake in response to physiologic need is associated with healthy weight gain trajectories.13,16 Responsive feeding occurs when a parent (or other caregiver) learns and recognizes the infant's cues of hunger and satiety, and responds promptly to these cues.18 The Dietary Guidelines for Americans recommend responsive feeding.19 Additionally, a recent systematic review found responsive feeding to be associated with healthy growth in children less than two years of age.13 Education on, and promotion of, responsive feeding should begin prenatally and evolve with the development of the child.18 Infant feeding during the first months after birth often occurs in the home, making this an ideal environment to promote responsive feeding.10,20-22 Interventions to promote responsive feeding have shown benefit in preventing rapid infant weight gain and promoting healthy dietary patterns in young children.20-28 However, this research has not been integrated using a validated coaching approach with the family's home. Additionally, responsive feeding has been largely measured via surveys.25 To address these gaps, an individualized responsive feeding coaching intervention, Learning Early Infant Feeding Cues (LEIFc), has been developed by the PI of the proposed study and her team.
The multicomponent LEIFc intervention involves maternal education on responsive feeding practices while using a family-guided caregiver coaching approach called SS-OO-PP-RR (Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) during feeding sessions.29,30 The SS-OO-PP-RR approach was developed based on adult learning theory and has been successfully used with parents and childcare providers to promote development across domains in infants and young children.29-31 For the LEIFc intervention, SS-OO-PP-RR was modified to be specific to communication during feeding to promote responsive feeding (Table 1). It is used as a guide for the interventionists during the coaching session but will also be used to evaluate the fidelity of the intervention. The purpose of this study is to test fidelity and feasibility of the LEIFc intervention in a group of diverse mother-infant dyads North Florida.
4.0 Study Endpoints* 4.1 The study will end when the participants complete all time points or the infant reaches 6 months of age.
5.0 Study Intervention
1.1 The investigators developed the LEIFc intervention based on the literature and prior pilot studies. The multicomponent LEIFc intervention involves maternal education on responsive feeding practices while using a family-guided caregiver coaching approach called SS-OO-PP-RR (Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) during feeding sessions.29,30 The SS-OO-PP-RR approach was developed based on the adult learning theory and has been successfully used with parents and childcare providers to promote development across domains in infants and young children.29-31 For the LEIFc intervention, SS-OO-PP-RR was modified to be specific to communication during feeding to promote responsive feeding. It is used as a guide for interventionists during the coaching session but will also be used to evaluate the fidelity of the intervention. The research study consists of five visits (Table 1) beginning in the third trimester (28 weeks and beyond) of pregnancy to four months after the infant's birth.
6.0 Procedures Involved* Design. This study uses a pre-post quasi experimental design with no control group to examine the feasibility, utility, and social validity of the LEIFc intervention. Videos will be coded prior to the intervention then after two coaching sessions between interventionist and mother during a feeding session. We will also use a pre-post measure to assess mother knowledge and beliefs regarding infant feeding practices. Demographic factors, post-partum depression, and maternal-infant bonding will be considered as covariates.
Instruments. Objective measurement of responsive feeding will occur through video coding and analysis of feeding sessions. The research team is in the process of developing a coding scheme. The Responsiveness to Child Feeding Cues Scale (RCFCS) 32 and literature from the communication arena 33-35 have been used to guide the coding scheme. Research assistants will be trained on the coding scheme and will use existing videos to code with a goal of at least 85% agreement achieved to confirm interrater reliability. Investigator Romano has significant experience with observational measurement.
The Infant Feeding Questionnaire (IFQ) is completed by mothers and provides a measure of infant feeding practices and beliefs.36 The 20-item questionnaire assesses for: concern for the infant being underweight, concern about hunger, awareness of hunger and fullness cues, concern about overweight, feeding on a schedule, providing food to calm an infant, and social interaction during feeding.36 Likert-type scoring is used, higher scores indicate a stronger measure of the construct. Investigator Bahorski has prior experience using this tool. 37,38 Infant feeding practices, including breastmilk, formula, and/or complementary foods, are collected at each visit, as well as reflective feedback from the interventionist. This instrument was developed by the investigators based on the literature and prior research. Infant height and weight will be collected using standard clinical techniques. The Patient Health Questionnaire-9 (PHQ-9) will provide a method to screen for depression at each visit as depression is known to influence infant feeding practices.39 The Maternal-to-Infant Bonding Questionnaire (MIBQ) will be also be collected at each visit; bonding will be used as a covariate.
Procedures:
Prenatal Intervention, Phase 1 (Visit 1). Teaching about responsive feeding practices before birth. This aspect of the intervention includes written and video materials about responsive feeding practices during the mothers' final weeks of her pregnancy. These practices include hunger and satiety cues, avoiding scheduled feedings and feeding to soothe, and how to make feeding times valuable contexts for mother-infant bonding and language learning. The materials will include examples of infant cues and will engage mothers to reflect on how these practices are similar to, or different from, what she has heard about feeding from family, friends, her community, or her healthcare provider. Additionally, the mother will complete the following surveys: demographics, prenatal infant feeding plans, depression (PHQ-9), and mother-infant bonding (MIBQ). This session will be held over the phone.
Pre-test (Visit 2). Approximately two weeks after the mother's due date, participants will be contacted to confirm continued eligibility in the study (full term birth of the infant, no complications at birth or unexpected infant anomaly). If the dyad remains eligible to participate in the study, study Visit 2 will occur when the infant is approximately 1 month of age. A feeding session with mother and infant will be videotaped in the home by the interventionist (or in the clinic if the mother prefers). Surveys will include birth history, current feeding practices, IFQ, PHQ-9, and MIBQ. Infant height and weight will also be collected.
Intervention Phase 2 (Visits 3 \& 4): The interventionist will conduct two study visits when the infant is approximately two and three months of age. These will be held within the family home at a time convenient to the mother (or in the clinic if the mother prefers). During these video-recorded coaching sessions, the interventionist will use a modified version of the SS-OO-PP-RR coaching approach to share the content about responsive feeding practices and responsive interactions. The mother will have a chance to practice these techniques with her infant with guidance and support from the interventionist. The mother and interventionist will also reflect and problem solve about how the interactions went and what potential adaptations could be made (i.e., if a mom is worried about wasting milk, how might they prepare bottles to account for responsiveness to a child's fullness cues). Current infant feeding practices will be collected at each visit and the PHQ-9 and MIBQ will be completed.
Post Test (Visit 5). The final visit will occur when the infant is approximately 4-5 months of age (but not more than 6 months). The interventionist will video record mother-infant interactions during a feeding as the post-test observational measure. The mother will also complete the IFQ, PHQ-9, and MIBQ; current infant feeding, infant height and weight will be collected. Maternal feedback on the intervention will be collected via open ended questions. Maternal response to questions will be audio recorded.
10.0 Subject Population* 10.1 Sample. Pregnant mothers (N = 50) aged 18 years or older, in their third trimester (28 weeks and beyond) of a healthy, singleton pregnancy will be recruited to participate in this study. Inclusion of this population of mothers will eliminate cofounding variables such as birth at either end of the age spectrum (i.e., teenage or advanced maternal age), caring for twins, or infants with complex medical conditions (i.e., congenital or genetic anomalies). Infants will be included once birth until infant age of 4-6 months. Only healthy, full-term infants with no congenital anomalies or medication conditions that would interfere with feeding and/or growth.
10.2 Women unable to provide consent will be excluded from participating along with incarcerated women.
10.3 Pregnant women and infants are included in this study.
- Conditions
- Responsive Infant Feeding, Infant Growth
- Being tested
- Learning Early Infant Feeding Cues (LEIFc)
- Keywords
- infants, infant feeding, breastfeeding, health promotion, infant growth, childhood obesity prevention
- Medical subject headings
- Breast Feeding
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Learning Early Infant Feeding Cues (LEIFc)Behavioural
Coaching sessions using SS-OO-PP-RR are conducted at infant age of 2 and 3 months. This occurs during an infant feeding session between mother and infant with the interventionists offering coaching specific to responsive feeding during the session. At the conclusion of the visit, the interventionists and mother develop specific strategies to practices prior to the next visit. At the following visit, a discussion of reflection and review occurs prior to the infant feeding session to identify what is going well and what still needs work.
| Study group | Role | What they receive |
|---|---|---|
| LEIFc | Experimental | The LEIFc intervention was developed by the research team and includes several key components, including a prenatal visit to introduce infants' early feeding cues and in the moment coaching supports during feeding routines after the baby is born. The SS-OO-PP-RR ("super," Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) coaching approach is a hallmark of the intervention that is intended to build caregiver confidence in reading their child's cues with in the moment practice and feedback as well as problem solving and reflecting on what is working or what needs to be adapted. Receives: Behavioral: Learning Early Infant Feeding Cues (LEIFc) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Responsive Infant Feeding
Subjective (via survey) and objective (via video) measurement of responsive feeding will be collected pre-post intervention visits. The Infant Feeding Questionnaire will provide a subjective measure of responsive feeding. A feeding session will be video recording then coded for instances of infant cues and maternal response to cues to provide an objective measure of responsive feeding.
Measured: Pre-intervention (infant age 1 month) to post-intervention (infant age 4 months)
Secondary outcomes (3)
Duration of Breastfeeding
Current infant feeding practices are collected at each study visit. Duration of any breastfeeding will be tabulated into a variable.
Measured: weeks since birth
Age of complementary food introduction
Current infant feeding practices are collected at each study visit. The infant age (in weeks) at which any foods other than breastmilk or formula were given will be tabulated into a variable.
Measured: weeks since birth
Infant weight-for-length z-score (WLz)
Infant WLz will be calculated from infant weight and length measurements obtained at each study visit. The difference in WLz between infant age of 2 weeks and 6 months will be calculated. Infants will be categorized into 3 growth categories: expected growth (WLz SD change between -0.67 and 0.67, rapid growth > or equal to 0.67, or slow growth < or equal to -0.67.
Measured: birth to 4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Mar 2025
- Study start10 Apr 2022
- Primary completion31 Oct 2023
- Study completion31 Oct 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Responsive Infant FeedingStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Obesity-Related Behavioral Intervention Trials (ORBIT)
- Masking
- None (open label)
- Enrolment
- 29 participants (actual)
Sponsor and investigators
- Lead sponsor
- Florida State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jessica Bahorski, Florida State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06898190
- Sponsor's protocol ID
- STUDY00002895
- Status last verified
- Mar 2025
- First submitted
- 16 Mar 2025
- Last updated
- 27 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: IPD may result in a breach of confidentiality, aggregated data may be shared via a DUA.
Publications
Bahorski J, Romano M, McDougal JM, Kiratzis E, Pocchio K, Paek I. Development of an Individualized Responsive Feeding Intervention-Learning Early Infant Feeding Cues: Protocol for a Nonrandomized Study. JMIR Res Protoc. 2023 Feb 28;12:e44329. doi: 10.2196/44329.
PubMed 36853761
Study at a glance
From the registry record, last updated by the sponsor on 27 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Testing the Feasibility & Fidelity of the Learning Early Infant Feeding Cues (LEIFc) Intervention
- ClinicalTrials.gov ID
- NCT06898190
- Acronym / sponsor ID
- STUDY00002895
- Conditions
- Responsive Infant Feeding, Infant Growth
- Keywords
- infants, infant feeding, breastfeeding, health promotion, infant growth, childhood obesity prevention
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 29 participants (actual)
- Lead sponsor
- Florida State UniversityUniversity, hospital or other
- Study start
- 10 Apr 2022 (actual)
- Primary completion
- 31 Oct 2023 (actual)
- Study completion
- 31 Oct 2023 (actual)
- First posted
- 27 Mar 2025 (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.
The reason that we are doing this research is to teach mothers ways to communicate with their baby during feeding. Understanding signals a baby gives helps mothers know when and how much to feed their baby which will help the baby grow in a healthy way.
There are 5 study visits, 1 during pregnancy and 4 after the baby is born. At the first visit participants will watch some videos about feeding babies and be provided with information to read about feeding babies, there is also a questionnaire to complete. After the baby is born, a research team member will come to participants' homes at infant age of 1, 2, 3, and 4 months to videotape an infant feeding session. At the visit when the baby is 2 and 3 months of age, the intervention will occur in which the interventionists will provide coaching about responsive feeding before and during a feeding session. The baby's height and weight will be collected and some questionnaires completed. At the last study visit, a research assistant will ask opened ended questions about the study itself, these questions and participant answers will be audio recorded.
Detailed description
3.0 Background* 3.1 and 3.3 Health disparities in pediatric obesity are staggering; Non-Hispanic black and Hispanic children have obesity rates (22.2% and 25.8% respectively) higher than the national average (18.5%) and higher than non-Hispanic white children (14.1%).1,2 Additionally, children of low socioeconomic status (SES) are more likely to have obesity.2,3 These same populations are disproportionately affected by lifelong cardiometabolic conditions that result from obesity such as hypercholesterolemia, hypertension, and type 2 diabetes.4 Children with obesity are also more likely to suffer from mental health disorders (i.e., depression, anxiety) and complications of the pulmonary, orthopedic, and gastrointestinal systems.2,5,6 Lifestyle modifications implemented early in life are key to preventing obesity and the resulting lifelong complications. The first 1,000 days of life, from conception to age two years, is a critical period for development of habits that contribute to one's weight status later in life, such as dietary preferences and behaviors.7-10 Therefore, interventions implemented during the first 1,000 days and targeting infants from high-risk groups have potential to decrease one's obesity risk and address racial/ethnic and socioeconomic health disparities.
Infant feeding practices, which include what and how infants are fed, are one such habit that could be modified to decrease obesity risk.5 Exclusive formula feeding, short duration of breastfeeding when initiated, and early introduction of complementary foods contribute to rapid infant weight gain which, in turn, contributes to higher risk for childhood obesity.11,12 Many initiatives have targeted "what" infants are fed (i.e., promoting breastfeeding and healthy dietary intake) whereas "how" infants are fed is also important, yet understudied.5,8,13,14 The responsive feeding approach is thought to promote the ability to recognize and respond to internal cues of hunger and satiety.13-17 The ability to recognize these internal cues and self-regulate intake in response to physiologic need is associated with healthy weight gain trajectories.13,16 Responsive feeding occurs when a parent (or other caregiver) learns and recognizes the infant's cues of hunger and satiety, and responds promptly to these cues.18 The Dietary Guidelines for Americans recommend responsive feeding.19 Additionally, a recent systematic review found responsive feeding to be associated with healthy growth in children less than two years of age.13 Education on, and promotion of, responsive feeding should begin prenatally and evolve with the development of the child.18 Infant feeding during the first months after birth often occurs in the home, making this an ideal environment to promote responsive feeding.10,20-22 Interventions to promote responsive feeding have shown benefit in preventing rapid infant weight gain and promoting healthy dietary patterns in young children.20-28 However, this research has not been integrated using a validated coaching approach with the family's home. Additionally, responsive feeding has been largely measured via surveys.25 To address these gaps, an individualized responsive feeding coaching intervention, Learning Early Infant Feeding Cues (LEIFc), has been developed by the PI of the proposed study and her team.
The multicomponent LEIFc intervention involves maternal education on responsive feeding practices while using a family-guided caregiver coaching approach called SS-OO-PP-RR (Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) during feeding sessions.29,30 The SS-OO-PP-RR approach was developed based on adult learning theory and has been successfully used with parents and childcare providers to promote development across domains in infants and young children.29-31 For the LEIFc intervention, SS-OO-PP-RR was modified to be specific to communication during feeding to promote responsive feeding (Table 1). It is used as a guide for the interventionists during the coaching session but will also be used to evaluate the fidelity of the intervention. The purpose of this study is to test fidelity and feasibility of the LEIFc intervention in a group of diverse mother-infant dyads North Florida.
4.0 Study Endpoints* 4.1 The study will end when the participants complete all time points or the infant reaches 6 months of age.
5.0 Study Intervention
1.1 The investigators developed the LEIFc intervention based on the literature and prior pilot studies. The multicomponent LEIFc intervention involves maternal education on responsive feeding practices while using a family-guided caregiver coaching approach called SS-OO-PP-RR (Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) during feeding sessions.29,30 The SS-OO-PP-RR approach was developed based on the adult learning theory and has been successfully used with parents and childcare providers to promote development across domains in infants and young children.29-31 For the LEIFc intervention, SS-OO-PP-RR was modified to be specific to communication during feeding to promote responsive feeding. It is used as a guide for interventionists during the coaching session but will also be used to evaluate the fidelity of the intervention. The research study consists of five visits (Table 1) beginning in the third trimester (28 weeks and beyond) of pregnancy to four months after the infant's birth.
6.0 Procedures Involved* Design. This study uses a pre-post quasi experimental design with no control group to examine the feasibility, utility, and social validity of the LEIFc intervention. Videos will be coded prior to the intervention then after two coaching sessions between interventionist and mother during a feeding session. We will also use a pre-post measure to assess mother knowledge and beliefs regarding infant feeding practices. Demographic factors, post-partum depression, and maternal-infant bonding will be considered as covariates.
Instruments. Objective measurement of responsive feeding will occur through video coding and analysis of feeding sessions. The research team is in the process of developing a coding scheme. The Responsiveness to Child Feeding Cues Scale (RCFCS) 32 and literature from the communication arena 33-35 have been used to guide the coding scheme. Research assistants will be trained on the coding scheme and will use existing videos to code with a goal of at least 85% agreement achieved to confirm interrater reliability. Investigator Romano has significant experience with observational measurement.
The Infant Feeding Questionnaire (IFQ) is completed by mothers and provides a measure of infant feeding practices and beliefs.36 The 20-item questionnaire assesses for: concern for the infant being underweight, concern about hunger, awareness of hunger and fullness cues, concern about overweight, feeding on a schedule, providing food to calm an infant, and social interaction during feeding.36 Likert-type scoring is used, higher scores indicate a stronger measure of the construct. Investigator Bahorski has prior experience using this tool. 37,38 Infant feeding practices, including breastmilk, formula, and/or complementary foods, are collected at each visit, as well as reflective feedback from the interventionist. This instrument was developed by the investigators based on the literature and prior research. Infant height and weight will be collected using standard clinical techniques. The Patient Health Questionnaire-9 (PHQ-9) will provide a method to screen for depression at each visit as depression is known to influence infant feeding practices.39 The Maternal-to-Infant Bonding Questionnaire (MIBQ) will be also be collected at each visit; bonding will be used as a covariate.
Procedures:
Prenatal Intervention, Phase 1 (Visit 1). Teaching about responsive feeding practices before birth. This aspect of the intervention includes written and video materials about responsive feeding practices during the mothers' final weeks of her pregnancy. These practices include hunger and satiety cues, avoiding scheduled feedings and feeding to soothe, and how to make feeding times valuable contexts for mother-infant bonding and language learning. The materials will include examples of infant cues and will engage mothers to reflect on how these practices are similar to, or different from, what she has heard about feeding from family, friends, her community, or her healthcare provider. Additionally, the mother will complete the following surveys: demographics, prenatal infant feeding plans, depression (PHQ-9), and mother-infant bonding (MIBQ). This session will be held over the phone.
Pre-test (Visit 2). Approximately two weeks after the mother's due date, participants will be contacted to confirm continued eligibility in the study (full term birth of the infant, no complications at birth or unexpected infant anomaly). If the dyad remains eligible to participate in the study, study Visit 2 will occur when the infant is approximately 1 month of age. A feeding session with mother and infant will be videotaped in the home by the interventionist (or in the clinic if the mother prefers). Surveys will include birth history, current feeding practices, IFQ, PHQ-9, and MIBQ. Infant height and weight will also be collected.
Intervention Phase 2 (Visits 3 \& 4): The interventionist will conduct two study visits when the infant is approximately two and three months of age. These will be held within the family home at a time convenient to the mother (or in the clinic if the mother prefers). During these video-recorded coaching sessions, the interventionist will use a modified version of the SS-OO-PP-RR coaching approach to share the content about responsive feeding practices and responsive interactions. The mother will have a chance to practice these techniques with her infant with guidance and support from the interventionist. The mother and interventionist will also reflect and problem solve about how the interactions went and what potential adaptations could be made (i.e., if a mom is worried about wasting milk, how might they prepare bottles to account for responsiveness to a child's fullness cues). Current infant feeding practices will be collected at each visit and the PHQ-9 and MIBQ will be completed.
Post Test (Visit 5). The final visit will occur when the infant is approximately 4-5 months of age (but not more than 6 months). The interventionist will video record mother-infant interactions during a feeding as the post-test observational measure. The mother will also complete the IFQ, PHQ-9, and MIBQ; current infant feeding, infant height and weight will be collected. Maternal feedback on the intervention will be collected via open ended questions. Maternal response to questions will be audio recorded.
10.0 Subject Population* 10.1 Sample. Pregnant mothers (N = 50) aged 18 years or older, in their third trimester (28 weeks and beyond) of a healthy, singleton pregnancy will be recruited to participate in this study. Inclusion of this population of mothers will eliminate cofounding variables such as birth at either end of the age spectrum (i.e., teenage or advanced maternal age), caring for twins, or infants with complex medical conditions (i.e., congenital or genetic anomalies). Infants will be included once birth until infant age of 4-6 months. Only healthy, full-term infants with no congenital anomalies or medication conditions that would interfere with feeding and/or growth.
10.2 Women unable to provide consent will be excluded from participating along with incarcerated women.
10.3 Pregnant women and infants are included in this study.
Study design
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Obesity-Related Behavioral Intervention Trials (ORBIT)
| Arm | Type | Receives |
|---|---|---|
| LEIFc | Experimental | Behavioral: Learning Early Infant Feeding Cues (LEIFc)The LEIFc intervention was developed by the research team and includes several key components, including a prenatal visit to introduce infants' early feeding cues and in the moment coaching supports during feeding routines after the baby is born. The SS-OO-PP-RR ("super," Setting the Stage, Observation and Opportunities, Problem Solving and Planning, Reflection and Review) coaching approach is a hallmark of the intervention that is intended to build caregiver confidence in reading their child's cues with in the moment practice and feedback as well as problem solving and reflecting on what is working or what needs to be adapted. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- pregnant in the 3rd trimester (28 weeks or beyond) of a healthy pregnancy
- pregnant with a single fetus
- 18 years or older
- no known complications or genetic anomalies of the infant that would interfere with feeding or growth after birth
- English or Spanish speaking
Key exclusion criteria (2 listed)
- mother less than 18 years
- will not have custody of the infant after birth
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 |
|---|---|---|
| Learning Early Infant Feeding Cues (LEIFc)Coaching sessions using SS-OO-PP-RR are conducted at infant age of 2 and 3 months. This occurs during an infant feeding session between mother and infant with the interventionists offering coaching specific to responsive feeding during the session. At the conclusion of the visit, the interventionists and mother develop specific strategies to practices prior to the next visit. At the following visit, a discussion of reflection and review occurs prior to the infant feeding session to identify what is going well and what still needs work. | Behavioural | LEIFc |
Primary outcome
Responsive Infant Feeding
Time frame: Pre-intervention (infant age 1 month) to post-intervention (infant age 4 months)
Subjective (via survey) and objective (via video) measurement of responsive feeding will be collected pre-post intervention visits. The Infant Feeding Questionnaire will provide a subjective measure of responsive feeding. A feeding session will be video recording then coded for instances of infant cues and maternal response to cues to provide an objective measure of responsive feeding.
3 secondary outcomes
Duration of Breastfeeding
Time frame: weeks since birth
Age of complementary food introduction
Time frame: weeks since birth
Infant weight-for-length z-score (WLz)
Time frame: birth to 4 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Mar 2025.
- Results publication: PubMed 36853761Bahorski J, Romano M, McDougal JM, Kiratzis E, Pocchio K, Paek I. Development of an Individualized Responsive Feeding Intervention-Learning Early Infant Feeding Cues: Protocol for a Nonrandomized Study. JMIR Res Protoc. 2023 Feb 28;12:e44329. doi: 10.2196/44329.
- Individual participant dataSharing planned: No. IPD may result in a breach of confidentiality, aggregated data may be shared via a DUA.
Related trials for Responsive Infant Feeding
Not yet recruiting
Learning Early Infant Feeding Cues
Responsive Feeding, Infants
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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Learning Early Infant Feeding Cues (LEIFc) in people with Responsive Infant Feeding and Infant Growth, run by Florida State University 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?
The sponsor lists 5 inclusion and 2 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: finished, as of the sponsor's last update on 27 Mar 2025. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Responsive Infant Feeding (time frame: Pre-intervention (infant age 1 month) to post-intervention (infant age 4 months)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06898190, which also lists 1 linked publication.
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 27 Mar 2025; AzTrials last refreshed its copy on 27 Oct 2026.