Breastfeeding Exclusive

12

Review clinical trials related to Breastfeeding Exclusive. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Impact of Chia Seeds on Human Breast Milk Composition

The investigators' over-arching hypothesis is that mechanical and compositional properties of chia seeds supplemented during lactation diminish obesity-induced intestinal inflammation and barrier dysfunction. The investigators hypothesize these changes will result in: 1) reduced maternal systemic inflammation (serum CRP and IL-6) and increased gut microbial diversity and richness, 2) reduced HM fat and inflammatory markers, metrics the research team have demonstrated differ in tandem with maternal metabolic health and 3) improved infant growth/body composition. To test these hypotheses, investigators will evaluate chia seed supplementation during lactation in a 6wk multi-site pilot RCT (Aim 1) and through translational studies using human enteroids (Aim 2).

Participants needed: 80
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of OklahomaUpdated: May 15, 2026Locations: 2
Eligibility criteria

pre-pregnancy BMI >25 kg/m² [+7]

Inability to understand English [+4]

Status: Not yet recruiting

Breastfeeding Education Support Tool

The proposed project seeks to evaluate the effectiveness and implementation of the Breastfeeding Education Support Tool for Baby (BEST4Baby) intervention, an mHealth-supported community-based peer counselor breastfeeding intervention for mothers in India. Given that rates of optimal infant feeding practices have remained stagnant over the past two decades in India, and that India is the most populous country and icontributes one-fifth of all global live births, this project could have major global health implications if the intervention is found to improve maternal breastfeeding practices and infant clinical outcomes. The project will also provide evidence needed to adopt BEST4Baby nationally and in other low resource communities.

Participants needed: 336
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Thomas Jefferson UniversityUpdated: May 5, 2026Locations: 1
Eligibility criteria

at least 18 years of age, [+7]

Status: Recruiting

Avocado Consumption, Nutrients in Human Milk, and Infant Cognitive Development

The goal of this interventional study is to establish a whole food, avocado, as a viable study material to supplement mothers and infants with nutrients that support optimal brain development. Eighty-eight breastfeeding dyads, 3m postnatal, will participate in this study designed to: 1. To document whether lactating mothers will comply in the consumption of 5 avocados a week for 12 weeks. 2. To ascertain the choline, lutein, and fatty acids present in human milk in women who eat avocado. 3. To measure the cognitive advantage conferred to infants whose mothers consume avocados while breastfeeding compared to a non-avocado-eating reference group. To this end, healthy, lactating women who are 13 weeks postpartum and their infants will be enrolled. Mothers will be provided avocados on a bi-weekly basis and will be asked to consume an avocado a day. Infant cognition will be tested when the infants are 4.5 and 6 months of age. Milk samples and diet data will be collected and assayed on a bi-weekly basis.

Participants needed: 88
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: University of North Carolina, Chapel HillUpdated: Apr 21, 2026Locations: 1
Eligibility criteria

Healthy lactating women at 13 weeks postpartum [+3]

Gestational diabetes [+3]

Status: Recruiting

Synergistic Activity of Human Milk Nutrients and Infant Cognition

Purpose: To establish a whole food, egg, as a viable study material to supplement mothers and infants with nutrients that support optimal brain development. There will be 84 breastfeeding dyads, 3 months postnatal. Mothers will be randomized to a whole egg or egg white (due to lack of an appropriate control food). Initial diet intake will be screened using the NDSR. Participants will come to the lab 3 times across 3 months (age 3 months, 4.5 months, and 6 months). Milk, saliva, and plasma will be collected from the mother, while saliva and plasma (heel stick) are collected from the infant. Diet data will be collected at each visit. The infant will complete a recognition memory test using electrophysiology at 6 months as well as the Bayley Scales of Infant Development at 4.5 months. The mother will complete a temperament questionnaire at 3 months and 6 months.

Participants needed: 84
Trial details
Age: 3-35Biological sex: AllType: InterventionalSponsor: University of North Carolina, Chapel HillUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

infant is 12-15 weeks of age at enrollment [+3]

infant with diagnosis or documented suspicion of developmental delay [+3]

Status: Recruiting

taVNS-Paired Breastfeeding to Improve Breastfeeding at Discharge

Investigators aim to improve the skills of premature or sick term infants in breastfeeding by boosting motor learning with transcutaneous vagus nerve stimulation. Investigators will recruit 10 premature, ≥ 35 weeks gestational age, or convalescing sick term infants admitted to the NICU at MUSC to participate in this study. Infants will receive taVNS treatments once a day with breastfeeding's for up to 14 days. Before each treatment, the researcher will determine how much electrical stimulation is needed for the infant to feel a slight tingle without discomfort, and during daily treatment paired with breastfeeding the infant will continue to receive this level of electrical stimulation, coinciding with latching and sucking, repeated over the duration of the feed. Investigators will collect information about the pre- and post-feed weights, the length of time for each feed, and observations of latch, suck, and swallow techniques by the infant from parents and the lactation consultant. Investigators will also evaluate parental satisfaction associated with their infant's ability to breastfeed after taVNS by providing parental satisfaction surveys at the beginning, after 1 and 2 weeks, and at 3 months after the end of the study to assess infants' progress in and maintenance of breastfeeding abilities. If the pairing of breastfeeding with taVNS is able to result in improved outcomes of effective breastfeeding in infants in the neonatal intensive care units, this intervention could be further utilized by NICUs to increase the rate of premature and sick term infants who are successfully able to breastfeed at the time of discharge and maintain breast feeding longer after discharge. This would allow premature infants to acquire the many benefits of breastmilk as well as contribute towards the strengthening of the maternal-infant bond that breastfeeding has been shown to enhance.

Participants needed: 10
Trial details
Age: 35+Biological sex: AllType: InterventionalSponsor: Medical University of South CarolinaUpdated: Feb 6, 2026Locations: 1
Eligibility criteria

Infants ≥ 35 weeks post-menstrual age, [+4]

Cardiomyopathy, [+5]

Status: Not yet recruiting

Breastfeeding: Influencing Determinants, Knowledge and Self-efficacy

Our study will assess the prevalence of exclusive breastfeeding and the determinants and assess knowledge and self efficacy of lactating mothers towards breastfeeding

Participants needed: 380
Trial details
Age: 15-49Biological sex: FemaleType: ObservationalSponsor: Sohag UniversityUpdated: Jan 13, 2026
Eligibility criteria

Mothers with absolute contraindications to breastfeeding as the infant having cl... [+1]

Status: Not yet recruiting

Effectiveness of a Counseling Program on Exclusive Breastfeeding Rates in a Primary Care Center

Introduction: Evidence supports that exclusive breastfeeding (EBF) is the most beneficial method of infant feeding up to 6 months of age. The practice confers numerous advantages for the infant and the mother. Many breasfeeding are abandoned early due difficulties experienced after dischargue and after returning to work. Development specific early breastfeeding support programs in the community is necessary to avoid unwanted abandonment. Objective: To analyse the differences in BF rates at six month of birth in healthy full-term newborns between the study groups. Methodology: Pilot study of a randomised clinical trial carried out in a Paediatric Nursing clinic at the Ventorrillo Health Centre in A Coruña. The study population will be mothers of healthy full-term newborns who wish to give BF at the time of delivery and whose reference health centre is the one of the study. The mother- newborn dyads in the control group (CG) will receive the usual care described in the child health Program of the Galician Health Service, and the dyads included in the intervention group (IG) will also receive specific advice on breastfeeding during the first 6 months of life. A study sample of 80 participants is estimated for each group. The study will be approved by the Research Ethics Committee of A Coruña-Ferrol. The variables under study will be collected in a data collection notebook for later statistical analysis. A significant value of p \< 0.05 being considered.

Participants needed: 160
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Fundacion Profesor Novoa SantosUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Mothers who express a desire to breastfeed during a follow-up consultation with... [+2]

Maternal age under 18 years - Maternal use of drugs or medication that prevent b... [+2]

Status: Recruiting

The Effect of Breastfeeding Counseling on Social Support Perception, Breastfeeding Self-Efficacy and Outcomes

The purpose of this study is to examine the effects of the Breastfeeding Self-Efficacy Resources Development Nurse Consultancy Program (EMÖZGEDAP), based on Dennis's Breastfeeding Self-Efficacy Theory along with the hypno-breastfeeding philosophy given to mothers and family relatives, on social support perception, breastfeeding self-efficacy and outcomes. The study will involve pregnant women and close others assigned randomly to the intervention (n=50) or control (n=50) groups in a state hospital in Turkey. Individual counseling will be provided to the intervention group within the scope of the EMÖZGEDAP, based on Denis's Breastfeeding Self-Efficacy theory and hypnobreastfeeding philosophy. EMÖZGEDAP, which will be applied to pregnant women and their family relatives, will consist of 5 sessions lasting 7.5 hours (2 sessions with the woman and her family relatives, two sessions with the woman alone, and one with her family relatives alone). The Antenatal Breastfeeding Self-Efficacy Scale will be evaluated before the counseling program is given in the antepartum period. Breastfeeding and Nutrition Results, Postpartum Breastfeeding Self-Efficacy Scale, Breastfeeding Self-Efficacy Scale for Fathers, Assessment Scale for Perceived Support of Close Others in Relation to Breastfeeding Self-Efficacy and Scale of Perception of Close Others' Support For Breastfeeding Self-Efficacy will be evaluated at the 1st, 3rd, and 6th months postpartum.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Ondokuz Mayıs UniversityUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Being 18 years or older, [+7]

Not filling out the forms in the study or filling them incompletely, [+4]

Status: Recruiting

MBSR and NLP, Postpartum Breastfeeding and Depression

The postnatal period is a risky period in which mothers experience regressive and progressive changes and rapid biopsychosocial changes. Since this process affects not only the mother but also the family, mothers are under intense stress due to adaptation to the changes that occur in this period.

Participants needed: 90
Trial details
Age: 19-35Biological sex: FemaleType: InterventionalSponsor: Aysegul KilicliUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

19-35 years old [+3]

women who refused to participate in the research.

Status: Not yet recruiting

MILC: A Comprehensive Mobile Application That Addresses the Breastfeeding Challenges of Low-income Hispanic Mothers

The innovative platform MILC is designed to provide an integrated and comprehensive professional and social support network with personalized breastfeeding (BF) education to target exclusive breastfeeding (EBF) and any BF behaviors in low-income Hispanic women. Formative research conducted for the development of MILC and results from pilot testing will help guide the completion of the development and testing of this prototype that specifically caters to Hispanic women. In the long term, MILC has the potential to increase the rates of EBF and any BF up to 12 months.

Participants needed: 178
Trial details
Age: 18-44Biological sex: FemaleType: InterventionalSponsor: Benten Technologies, Inc.Updated: Jul 26, 2024Locations: 3
Eligibility criteria

Mothers who successfully exclusively breastfed for up to 6 months, at least one... [+13]

Participants who are under the age of 18 or over 44 [+12]

Status: Not yet recruiting

Providing Breastfeeding Support After Discharge From Hospital to Improve Growth and Development of Malnourished Infants

The current guidelines used to manage malnutrition among infants aged below 6 months (u6m) recommend that infants admitted to hospital with malnutrition be supported to reestablish exclusive breastfeeding before discharge. Studies have shown that reestablishing exclusive breastfeeding among infants being treated for acute malnutrition is possible. However, follow-up of the infants after discharge has revealed poor growth raising questions about what happens to infant feeding practices after discharge and whether providing breastfeeding support to mothers after discharge would help improve the recovery and growth of their infants. Providing a package of home-based care with breastfeeding support to mothers of infants u6m recovering from acute malnutrition has the potential to improve the retention of exclusive breastfeeding and lead to enhanced infant growth and survival. To date, no such post-discharge package of care is available in Kenya or other lower and meddle income countries (LMICs). The aim of this study is to apply participatory, qualitative and quantitative approaches to develop and evaluate the impact of a post-discharge package of care on the growth and development of acutely ill malnourished infants after discharge from hospital.

Participants needed: 250
Trial details
Age: 4-12Biological sex: AllType: InterventionalSponsor: University of OxfordUpdated: Apr 18, 2024
Eligibility criteria

Any possibility to breastfeed (carer of reproductive age willing to breastfeed a... [+1]

Status: Not yet recruiting

Impact of a Mobile Health Breastfeeding Counseling Intervention for Employed Mothers in Kenya

Exclusive breastfeeding (EBF) is critical for child survival, growth, and maternal health; however, over half of mothers in low and middle-income countries (LMIC). Mobile health (mHealth) describes a range of wireless technologies and techniques that seek to increase patient access to and interaction with preventive health services. This study will develop and test the feasibility of an mHealth intervention to improve support counseling for breastfeeding at a large sub-county referral hospital in Naivasha, Kenya.

Participants needed: 284
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Wheaton CollegeUpdated: Nov 16, 2022
Eligibility criteria

Mothers over 18 years who are employed in contract-based labor in sectors that i... [+1]

Mothers of infants with cleft deformities or other abnormalities that interfere...