Clinical Trials Logo

Breastfeeding clinical trials

View clinical trials related to Breastfeeding.

Filter by:

NCT ID: NCT02819193 Completed - Breastfeeding Clinical Trials

Using Mother's Raw Milk Could Improve Breastfeeding in Hospitalized Neonates

DOAL
Start date: April 2012
Phase: N/A
Study type: Observational

Despite the importance of breast milk for sick or preterm neonates, there is currently no consensus regarding the use of raw mother's own milk (MOM) in neonatal units. The aims of this study are to: (a) describe factors associated with the use of raw MOM; (b) investigate the association between early use of raw MOM and breastfeeding continuation at discharge and up to 6 months later.

NCT ID: NCT02756169 Completed - Breastfeeding Clinical Trials

Maternal Obesity and Breastfeeding Performance

Start date: July 14, 2016
Phase: N/A
Study type: Interventional

Investigators propose this study in order to answer the following research question: An educational intervention and breastfeeding support at postpartum will increase the frequency and total breastfeeding duration in the intervention group? This is a randomized (with control and intervention groups) study, open and parallel (1: 1 ratio between study groups) with 200 pregnant women in the second or third trimester, according to their body mass index (BMI, kg / m2) with excess weight (BMI> 29 pre-pregnancy weight) and that will address their pregnancy in the public health services and hospitals belonging to the Health Ministry of 5 districts: Coyoacán, Magdalena Contreras, Tlalpan, Xochimilco and Alvaro Obregón in Mexico City. The intervention group and the control group will have the same characteristics for eligibility. The main phases to develop the study are PHASE 1. INTERVENTION DESIGN PHASE 2. IMPLEMENTATION OF THE INTERVENTION. PHASE 3. FOLLOW-UP The intervention will be offered at 3 times: 1) Educational intervention (a workshop) to pregnant obese women. The workshop will be held by an International Board Certified Lactation Consultant (IBCLC) to promote exclusive breastfeeding and to encourage a better breastfeeding performance in accordance with the WHO recommendations. The workshop will be held at convenient times and will be conducted for groups of 8 to 10 participants; 2) Immediate breastfeeding support at hospital by an IBCLC and; 3) The women will be exposed to early telephonic follow-up during the first week of their children´s lives and each month until six months of life. Then, if the breastfeeding continues, every two months until the first year of their children´s life. At the first month postpartum, investigators will visit participants at home, both the control group and the intervention group, for collecting information on breastfeeding practices, for taking a breast milk sample to estimate its fatty acids content, and a blood sample (serum) to obtain the C-Reactive Protein. Also, the investigators will take anthropometric measurements of the children to evaluate their growth (weight, length, and skinfold thickness). Investigators will ask for breastfeeding practices and diet of the participants through a 24 hours recall. The results of this intervention group will be compared with the control group: pregnant obese women without educational intervention or telephonic follow-up.

NCT ID: NCT02740842 Completed - Breastfeeding Clinical Trials

A Follow-up Study on the Sustained Impact of Alive & Thrive Interventions on Infant and Young Child Feeding Practices

Start date: April 2016
Phase: N/A
Study type: Interventional

Alive & Thrive (A&T) is a multi-year initiative to improve infant and young child feeding (IYCF) practices. During Phase 1 (A&T-1, 2009-2014), funded by the Bill & Melinda Gates Foundation, A&T aimed to reduce undernutrition and death caused by suboptimal IYCF practices in three countries - Bangladesh, Ethiopia, and Viet Nam. In 2014, IFPRI in collaboration with DATA conducted the endline survey in Bangladesh. The overall findings of the evaluation indicate that A&T's work in Bangladesh is a remarkable success story of scaling up what has been challenging to date in the field of nutrition: complex, high intensity and at-scale behavior change communications interventions. In 2016, a follow up study will be conducted to determine the sustained impacts on IYCF practices, expansion of operations and promoted practices into new areas, and diffusion of IYCF information, two years after the termination of external project support.

NCT ID: NCT02738957 Completed - Breastfeeding Clinical Trials

Effect of Prenatal Counseling on Breastfeeding Rates in Twins

Start date: September 2009
Phase: N/A
Study type: Interventional

Few studies have investigated breastfeeding in twins, and none have addressed the effect of antenatal counseling on breastfeeding twins.The purpose of this study is to investigate the effect of antenatal breastfeeding counseling on the breastfeeding rates in twin pregnancies.

NCT ID: NCT02642133 Completed - Breastfeeding Clinical Trials

Breastfeeding Improvement Following Tongue-tie and Lip-tie Release

Start date: June 2014
Phase: N/A
Study type: Interventional

This study is an observational study to determine outcomes of surgical release of tongue-tie and lip-tie in babies who are experiencing difficulty with breastfeeding.

NCT ID: NCT02639663 Not yet recruiting - Breastfeeding Clinical Trials

Dental Support Device During Breastfeeding as a Mean for Pain Control

Start date: January 2016
Phase: Phase 3
Study type: Interventional

Leboride is a dental support device that was developed for reducing pain during active labor. It is made of an inert material, placed in the woman's mouth and does not disturb breathing, talking, or any other activity expected during labor. It is a single-use device, each user receives a new one. This study hypothesis is that the Leboride use can reduce pain during breastfeeding, by that improve women's breastfeeding experience, and increase breastfeeding rates.

NCT ID: NCT02581800 Completed - Breastfeeding Clinical Trials

Effect and Experience of PreHomeCare of Preterm Infants Using Telecommunication and Smartphone Application

Start date: November 2015
Phase: N/A
Study type: Interventional

Background: Premature infants and their patents are discharged earlier from hospital and sent home in early in-homecare programs. Research regarding the use of health IT is needed to say, whether the use of videoconference and Smartphone application is a viable option to address the parents need for support in relations to early discharge. Aim: Test and explore early in-homecare (PreHomeCare) with videoconference and mobile application versus hospital consultations. Method: Main study; a randomized controlled intervention study with the hypothesis; parent of premature infants who have access to electronic knowledge and participatory guidance 24-7: increases proportion of exclusive breastfeeding, Improves parent/infant interaction, enhances confidence and increases knowledge. Sub study 1; a field study. Sub study 2; an interview study. Perspectives: It is expected that this project will be an argument in development of care for premature infants and telemedicine use in the future

NCT ID: NCT02574494 Completed - Hypertension Clinical Trials

Does Breastfeeding Lower Blood Pressure in Postpartum Hypertensive Patients

Start date: October 2015
Phase:
Study type: Observational

The primary aim is to establish whether breastfeeding is associated with lowering blood pressure in hypertensive women.

NCT ID: NCT02438878 Completed - Breastfeeding Clinical Trials

Supporting Baby Behavior Through Pediatric Offices

Start date: March 2015
Phase: N/A
Study type: Interventional

The primary objective of this project is to evaluate the impact on infant growth and infant-feeding practices of a low-cost series of video trainings and tools targeted to medical staff and designed to support ongoing Baby Behavior education of WIC participants.

NCT ID: NCT02407860 Completed - Breastfeeding Clinical Trials

Efficacy of an Osteopathic Treatment for Mechanical Sucking Dysfunctions in Newborn

Start date: December 2014
Phase: N/A
Study type: Interventional

Breastfeeding is the physiological and recommended way of feeding newborns as indicated by the World Health Organization, Health Canada and the politics of perinatality 2008-2018 in Quebec. Despite these, mothers who exclusively breastfed their babies are rare. According to Statistics Canada, the first month of life is the most at risk time to wean because of technical difficulties (53% of weaning) including mechanical issues. In Quebec city, despite a supportive network of health care professionals including lactation consultant, many babies are weaned. Lactation consultant are often feeling helpless when facing these mechanical difficulties. The purpose of this study is to determine the efficiency of an osteopathic treatment for newborns presenting breastfeeding mechanical difficulties. The investigators' hypotheses is that an osteopathic treatment integrating in the usual care is more efficient than usual car alone to help healing mechanical breastfeeding issues. The investigators propose a randomized clinical trial on a sample of 90 babies (45 in each group), under six weeks, presenting sucking dysfunctions, in Quebec city (Canada). The control group will receive usual care with a lactation consultant and the intervention group will receive usual care plus an osteopathic treatment. It is a simple blind clinical trial: the osteopath finds out, prior to evaluating the patient, what intervention should be delivered to the baby (assessment alone or standardized osteopathic treatment for infant). The results will ultimately lead to improvements in the existing knowledge on the fields of osteopathy and lactation support, allowing implementation of osteopathic care in the perinatal network.