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Breast FeedingNCT02952950

Is it Possible to Prolong the Duration of Breastfeeding in Premature Infants? a Prospectivt Study

A study testing Oralstimulation in people with Breast Feeding and Premature Birth, run by Hvidovre University Hospital at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In this project three studies examined two possible explanations and one possible preventive intervention to early cessation of exclusively breastfeeding in premature infants. Study 1 The content of protein in the milk of mothers, who delivers prematurely, is about a third higher than in the milk from the mother who… Read more about this study

Who is it for?
Ages Up to 37 weeks
Conditions the study is for
Breast Feeding, Premature Birth
What is being tested?
Oralstimulation
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
211 participants
Where
1 siteDenmark
Study dates
Sep 2016to Aug 2019
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 Up to 37 weeks
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • mothers: with premature infant i.e. the infant's gestational age is equal to or maximum of 36 + 6
  • intend to breastfeed.
  • The mother or father / other primary caregiver understand Danish, Norwegian, Swedish or English.

Who cannot join

  • mothers: will not / can´t breastfeed because of illness or abuse such as: HIV and drugs.
  • In addition, if the infant has a disability which makes it difficult to breastfeeding or if the infant is physiologically unstable, for example due to reduced lung function.

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Paediatric Department section Neonatology

    Hvidovre, Copenhagen, 2650

Other trials in Denmark

About this study

Official title: Is it Possible to Prolong the Duration of Exclusive Breastfeeding in Premature Infants? a Prospectivt Study

In this project three studies examined two possible explanations and one possible preventive intervention to early cessation of exclusively breastfeeding in premature infants.

Study 1 The content of protein in the milk of mothers, who delivers prematurely, is about a third higher than in the milk from the mother who delivers on time. The nutritional composition changes over time and the content of protein decrease. Therefore the premature infant is at risk of protein deficiency. While the infant is feeding by tube this decreasing content of protein can made up by adding, while it is more difficult when the infant is exclusively breastfeeding. The hypothesis is that reduced protein content in breast milk is associated to a fewer number of days where the premature infant is exclusively breastfed.

Read more

Study 2 The premature infant is characterized with immature muscle with a low tension and therefore, a low ability to eat its needs by breastfeeding the first period. The transfer of milk from mother to child is an interaction between the mothers and her milk ejection reflex that establish a positive pressure on the milk and the child that have to establish a vacuum. The hypothesis is that the premature infants suction power is too weak to establish sufficient intraoral vacuum to ensure milk transfer from the breast to the infant and it can be related to a fewer number of days where the infant is exclusively breastfed.

Study 3 The premature infants low muscle tone and its immaturity also influence on the organization and the quality of movements, marked as neuro motor processes. These processes form the oral motor base supporting movement which involves the infant ability to establish vacuum. The hypothesis is that Oral Stimulation for a specific program in 5 minutes before the minimum 2 meals per. day for at least 14 days increases the preterm infant's ability to create intra oral vacuum and thus the power to transfer milk from the breast, thereby extending the number of days when the infant is exclusively breastfed.

200 infants are included consecutively, as a recurring cohort in all 3 studies. In Study 1 the mothers' milk is analyzed in order to the content of protein. In Study 2 the infant suction is assessed by vacuum measurement. In study 3 the families are randomized to an intervention or control group and parents off 100 infants are guided by occupational therapists in a program of oral stimulation of their child.

Read the detailed description

The purpose of this project, which consists of three studies, is to investigate whether insufficient protein in breastmilk and / or inadequate intra oral vacuum of the infant can explain early breastfeeding cessation in the premature infant. Furthermore to test whether the breastfeeding period may be extended by oral stimulation.

The rate of breastfeeding in mothers of infants born prematurely is lower than in mothers who give birth on time. A Danish survey shows that about 70% of premature are on exclusive breastfeeding at discharge and that this rate is decreasing to about 30% six weeks after discharge. Breastmilk is the healthiest nutrition for the newborn and based on WHO's strategy for the feeding of infants Board of Health recommends that newborn infants, including premature, as far as possible are exclusively breastfed for six months. Exclusively breastfeeding means that the infant only gets the breastmilk of the mother. Exclusively breastfeeding has health implications for both mother and infant. Breastfeeding reduces lactation incidence of infectious diseases, improves cognitive development and visual function in the infant and reduces the risk of developing later obesity. In addition, the level of immune protective factors and anti-inflammatory elements is high in the mother's milk to the preterm infant and therefore reduce the infant's increased risk of early and severe infections, and death late effects. Furthermore, breastfeeding may reduce the risk of premature infant's abnormal vessel growth in the eye, and appears to have a protective effect on the disease being of significant excess mortality primarily attack the intestines of the preterm infant (necrotizing enterocolitis).

Problem Area / factors in milk composition with the importance of breastfeeding Breastmilk contains the necessary nutritional components and energy that the infant needs. Therefore, the milk of the mother delivering early have a higher content of fat and protein, and thereby a higher level of energy comparing with the milk from the mother who have given birth to term. The content of protein in the milk of the mother who gives birth prematurely is about 12 grams per liter and thus approximately one-third higher than that from the mother who gives birth on time. The nutritional composition of breastmilk vary considerably over time and the content of protein is decreasing why the premature infant are at risk of protein deficiency and thereby insufficient growth. During the hospital stay, and while the infant are feed by tube this decreasing protein content are made up by adding, while it is more difficult when the infant breastfeed exclusively. Protein is important for the infant's growth and strength and a local statement from Hvidovre Hospital found that 18% of all hospitalized preterm infants in 2014 were added additional protein to breastmilk, because growth was not sufficient. The question is whether reduced protein content in breastmilk has a correlation with the number of days where preterm infants are exclusively breastfed?

Problem Area / intra oral vacuum strength of the infant with significance for breastfeeding The period from birth to the premature infant feed exclusively at the breast without supplementary tube feeding varies from weeks to months, depending on how early the infant is born. The premature infant is characterized as being immature and with low muscle tone and therefore, a decreased ability to breastfeed the first time. The transfer of milk from mother to infant is an interaction between the mother and her milk ejection reflex creates a positive pressure on the milk and the infant creates a vacuum. If the infant not create a vacuum at the back of the mouth, the nipple of the mother is just pushed together and the infant is not transferred milk from the breast to the oral cavity. The amount of milk is regulated in relation to demand and a weak or shortage of vacuum will cause a shortage of milk transfer, which in turn physiologically will lead to less milk production and thereby decreasing amount. Studies that investigates this process and measured intra oral vacuum, shows all the importance of the infant's contribution by milk transfer, but does not answer to the extent the premature infants ability to create vacuum importance of breastfeeding establishment and maintaining. The question is whether the premature infants sucking strength is too weak to establish sufficient intraoral vacuum to ensure milk transfer from the breast to the infant and it can be related to a fewer number of days where the infant is exclusively breastfed.

In addition to the premature infants muscle tone has its immaturity also affect the organization and quality of body movements. Organization and quality in the movements may be referred to neuro motor processes and form among others the oral motor base supporting the movements involving the infant's ability to create vacuum. The processes preceding the creation of vacuum and studies have shown that by early intervention with oral stimulation in the form of stimulation of the nerves and muscles in and around the mouth, it can be oral motor basis strengthened. Studies where the infant carefully is stimulated with a finger, showing that the premature infant's muscles and sucking reflex can be influenced so that it is able to suck a larger volume in a shorter time in the bottle compared to the infant that is not stimulated orally. This presents an opportunity to influence the premature infant´s strength and maybe increase the ability to create intra oral vacuum affected by oral stimulation as a skill the infant preserves. The question is whether oral stimulation can increase the premature infant's ability to create vacuum and thus increase the power to transfer milk from the breast and thereby extending the number of days when with exclusively breastfed? The 3 studies are based on the same cohort. The cohort is identified and recruited at the Neonatal Intensive Care Unit at Hvidovre Hospital and relevant families where the mother delivers prematurely are included consecutively in accordance to the inclusion and exclusion criteria. The cohort will be demographically representative of everyday life in clinical practice with various family formation, education levels and socio-economic background conditions.

Power calculations are based primary outcome: exclusively breastfeeding duration and made to show effect on exclusively breastfeeding duration between the intervention- and the control group. Requirements for power calculation are a mean value of the vacuum set at 100% with a standard deviation (SD) of 26%. To detect the smallest clinically relevant difference of 13%, equivalent to half a SD and with an expected drop out of 20%, which included 200 infants (100 infants in each group) in the study (alpha = 0.05 and beta = 0.1 ). There hospitalized annually on average 300 preterm infants in the neonatal section. It is expected about 100 infants to meet the criteria for inclusion, thus achieved at approximately 2 year.

By inclusion the family is anonymized by allocating an ID number. When multiple assigned each infant this ID number and a one of letters a, b or c. All data and all measurements is obtained / made and recorded as far as possible of the project manager or alternatively the project nurse.

6 weeks after the date for the expected terminator date either the family are visiting the Neonatal section or the project manager/project nurse visiting the family in order to a status of breastfeeding, vacuum measurement and the infant's growth. In addition the family is contact by telephone the week in which the infant's postnatal age is 6 months. Here is recorded breastfeeding status, the time of any termination of exclusive breastfeeding and the infant's weight at GP visit 5 month old. The infant's growth is defined by its naked weight, Length and head circumference. Previous studies show a number of factors which affect breastfeeding duration. Features concerning socio-demographic background variables, perinatal and psychosocial conditions will gathered by the project manager or project nurse using a questionnaire in an interview with the family and form data in the analyzes. Participation in the project is safe and not associated with risk or discomfort for either mother or infant.

STUDY 1 / PROTEIN IN BREASTMILK Data are obtained in the human milk section at the hospital. Volume is obtained in milliliter (ml.) and protein content in gram pr. 100 ml. by using Miris Human Milk Analyzer according to the usual practice. Miri is the only European equipment that analyzes human milk. The test sample is 10 milliliters and the result given within a minute and logged into the machine and then transferred to the project database. When the mother is exclusively breastfeeding, we ask for 10 ml. Manual hand compressed breast milk. The analyzed milk can´t be reused and is therefore destroyed.

STUDY 2 / WEEK STRENGTH ASSESSMENT BY VACUUM MEASUREMENT Sucking strength of the premature infant is defined as the ability to create intra oral vacuum during sucking.

The intra oral vacuum of the premature infant is assessed by measuring the vacuum in the unit of mBar and are primary made by the project manager which is blinded to know if the infant has received oral stimulation or not. The measurement is made when the infant is awake and show readiness to suck. For vacuum measurement is a manometer selected with a bottle pacifier, which fits a Calmaflaske made by the firm Medela. The pacifier is shaped and is similar in function a breast and extra small so that it matches the premature mouth of a premature infant. As in a completely closed system the sucking of the infant is registered on this connected manometer. In order to obtain a measure of reproducibility of the method all vacuum measurements is carried out at 3 consecutive measurements. The advantage of the 3 measurements within a short time is to determine the intra-individual variability, but only if the infant is motivated and show redlines for measurement 3 times. The equipment is developed in cooperation with the Technical University of Denmark.

STUDY 3 / randomized INTERVENTION STUDY / ORAL STIMULATION Infants whose mothers is included in the cohort is randomized to receive / not receive oral stimulation when the infant's postnatal age is at least 32 + 0 weeks, as it is the time when the infant is able to coordinate sucking and swallowing reflex. In multiple birth all infants is randomized to the same group. The list is generated block randomized in blocks of 10

Families were randomized to the intervention group granted in total one hour instructions in a program of oral stimulation by one of two occupational therapists with experience in oral stimulation of preterm infants. The program is in collaboration with the project team developed and described by the Department of Physiology and Occupational therapy at Hvidovre Hospital. The first guidance for parents has duration of approximately half an hour and then follow-up once or twice, depending on the needs of the family. To maintain consistent intervention over time is the program of oral stimulation written in a script, where the family also must record the following variables: date and time of oral stimulation. In occupational therapy the guidance and in the script examines the signs that the infant exhibits when it is ready / not ready for stimulation. The family also sees a movie where these signs and the program of oral stimulation review auditory and visual. Families in the control group is not seeing the movie, do not receive the script or the supervision of occupational therapists and these infants do not get oral stimulation. Both groups receive instructions after usual practice i.e. guidance and elements that promote breastfeeding example, skin to skin contact and compression.

Being tested
Oralstimulation
Keywords
Intra Oral Vacuum, protein content breastmilk
Medical subject headings
Breast Feeding, Premature Birth

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OralstimulationOther

    The intervention group granted in total 1 hour instructions in a program of oral stimulation by one of two occupational therapists with experience in oral stimulation of preterm infants. The first guidance for parents has duration of approximately half an hour and then follow-up once or twice, depending on the needs of the family. To maintain consistent intervention over time is the program of oral stimulation written in a script, where the family also must record the following variables: date and time of oral stimulation. In occupational therapy the guidance and in the script examines the signs that the infant exhibits when it is ready / not ready for stimulation. The family also sees a movie where these signs and the program of oral stimulation review auditory and visual.

Study groups in NCT02952950
Study groupRoleWhat they receive
OralstimulationOtherInfants whose mothers is included in the cohort is randomized to receive oral stimulation when the infant's postnatal age is at least 32 + 0 weeks, as it is the time when the infant is able to coordinate sucking and swallowing reflex
Receives: Other: Oralstimulation
ControlgroupNo interventionFamilies in the control group is not seeing the oralstimulation movie, do not receive the script or the supervision of occupational therapists and these infants do not get oral stimulation. Both groups receive instructions after usual practice i.e. guidance and elements that promote breastfeeding example, skin to skin contact and compression.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Duration of Breastfeeding

    Exclusively breastfeeding duration measured in number of whole days and defined as the infant is exclusively fed with breastmilk

    Measured: 6 month

Secondary outcomes (2)
  1. Content of protein in breastmilk

    Protein content are examined once a week as long the family is hospitalized and 6 weeks after the terminator date.

    Measured: 6 weeks after the terminator date

  2. Intra Oral Vacuum

    Intra oral vacuum are examined once a week as long the family is hospitalized and 6 weeks after the terminator date.

    Measured: 6 weeks after the terminator date

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Nov 2016 (estimated)
  2. Study startSep 2016
  3. Primary completionSep 2018
  4. Study completionAug 2019

Resources

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
211 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02952950
Sponsor's protocol ID
H-16000621
Status last verified
Feb 2018
First submitted
1 Nov 2016
Last updated
25 Sep 2019
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Maastrup R, Hansen BM, Kronborg H, Bojesen SN, Hallum K, Frandsen A, Kyhnaeb A, Svarer I, Hallstrom I. Factors associated with exclusive breastfeeding of preterm infants. Results from a prospective national cohort study. PLoS One. 2014 Feb 19;9(2):e89077. doi: 10.1371/journal.pone.0089077. eCollection 2014.

    PubMed 24586513
  • Pimenta HP, Moreira ME, Rocha AD, Gomes SC Jr, Pinto LW, Lucena SL. Effects of non-nutritive sucking and oral stimulation on breastfeeding rates for preterm, low birth weight infants: a randomized clinical trial. J Pediatr (Rio J). 2008 Sep-Oct;84(5):423-7. doi: 10.2223/JPED.1839. English, Portuguese.

    PubMed 18923786
  • Wambach K, Riordan J, redaktører. Breastfeeding and human lactation. Fifth edition. Burlington, Massachusetts: Jones & Bartlett Learning; 2015.

  • Cope MB, Allison DB. Critical review of the World Health Organization's (WHO) 2007 report on 'evidence of the long-term effects of breastfeeding: systematic reviews and meta-analysis' with respect to obesity. Obes Rev. 2008 Nov;9(6):594-605. doi: 10.1111/j.1467-789X.2008.00504.x. Epub 2008 Jun 12.

    PubMed 18554244
  • Vohr BR, Poindexter BB, Dusick AM, McKinley LT, Higgins RD, Langer JC, Poole WK; National Institute of Child Health and Human Development National Research Network. Persistent beneficial effects of breast milk ingested in the neonatal intensive care unit on outcomes of extremely low birth weight infants at 30 months of age. Pediatrics. 2007 Oct;120(4):e953-9. doi: 10.1542/peds.2006-3227.

    PubMed 17908750
  • Cristofalo EA, Schanler RJ, Blanco CL, Sullivan S, Trawoeger R, Kiechl-Kohlendorfer U, Dudell G, Rechtman DJ, Lee ML, Lucas A, Abrams S. Randomized trial of exclusive human milk versus preterm formula diets in extremely premature infants. J Pediatr. 2013 Dec;163(6):1592-1595.e1. doi: 10.1016/j.jpeds.2013.07.011. Epub 2013 Aug 20.

    PubMed 23968744
  • Groh-Wargo S, Sapsford A. Enteral nutrition support of the preterm infant in the neonatal intensive care unit. Nutr Clin Pract. 2009 Jun-Jul;24(3):363-76. doi: 10.1177/0884533609335310.

    PubMed 19483066
  • Smith JP, Harvey PJ. Chronic disease and infant nutrition: is it significant to public health? Public Health Nutr. 2011 Feb;14(2):279-89. doi: 10.1017/S1368980010001953. Epub 2010 Jul 13.

    PubMed 20624333
  • Hylander MA, Strobino DM, Pezzullo JC, Dhanireddy R. Association of human milk feedings with a reduction in retinopathy of prematurity among very low birthweight infants. J Perinatol. 2001 Sep;21(6):356-62. doi: 10.1038/sj.jp.7210548.

    PubMed 11593368
  • McGuire W, Anthony MY. Donor human milk versus formula for preventing necrotising enterocolitis in preterm infants: systematic review. Arch Dis Child Fetal Neonatal Ed. 2003 Jan;88(1):F11-4. doi: 10.1136/fn.88.1.f11.

    PubMed 12496220
  • Agostoni C, Buonocore G, Carnielli VP, De Curtis M, Darmaun D, Decsi T, Domellof M, Embleton ND, Fusch C, Genzel-Boroviczeny O, Goulet O, Kalhan SC, Kolacek S, Koletzko B, Lapillonne A, Mihatsch W, Moreno L, Neu J, Poindexter B, Puntis J, Putet G, Rigo J, Riskin A, Salle B, Sauer P, Shamir R, Szajewska H, Thureen P, Turck D, van Goudoever JB, Ziegler EE; ESPGHAN Committee on Nutrition. Enteral nutrient supply for preterm infants: commentary from the European Society of Paediatric Gastroenterology, Hepatology and Nutrition Committee on Nutrition. J Pediatr Gastroenterol Nutr. 2010 Jan;50(1):85-91. doi: 10.1097/MPG.0b013e3181adaee0.

    PubMed 19881390
  • Sakalidis VS, McClellan HL, Hepworth AR, Kent JC, Lai CT, Hartmann PE, Geddes DT. Oxygen Saturation and Suck-Swallow-Breathe Coordination of Term Infants during Breastfeeding and Feeding from a Teat Releasing Milk Only with Vacuum. Int J Pediatr. 2012;2012:130769. doi: 10.1155/2012/130769. Epub 2012 May 9.

    PubMed 22844300
  • Boiron M, Da Nobrega L, Roux S, Saliba E. Pharyngeal swallowing rhythm in response to oral sensorimotor programs in preterm infants. J Neonatal Nurs. 2009;15(4):123-8.

  • Geddes DT, Sakalidis VS, Hepworth AR, McClellan HL, Kent JC, Lai CT, Hartmann PE. Tongue movement and intra-oral vacuum of term infants during breastfeeding and feeding from an experimental teat that released milk under vacuum only. Early Hum Dev. 2012 Jun;88(6):443-9. doi: 10.1016/j.earlhumdev.2011.10.012. Epub 2011 Nov 26.

    PubMed 22119233
  • Morris SE. Development of oral-motor skills in the neurologically impaired child receiving non-oral feedings. Dysphagia. 1989;3(3):135-54. doi: 10.1007/BF02407132.

    PubMed 2517923

Questions about this trial

What is this clinical trial studying?

A study testing Oralstimulation in people with Breast Feeding and Premature Birth, run by Hvidovre University Hospital at 1 site in Denmark.

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 3 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 25 Sep 2019. 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 Denmark. 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?

Duration of Breastfeeding (time frame: 6 month). 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 NCT02952950, which also lists 27 linked publications.

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 25 Sep 2019.

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