Evidence map›Paper›PMID 28683833›Full record

Trial reportBMC pediatrics2017

Effectiveness of skin-to-skin contact versus care-as-usual in mothers and their full-term infants: study protocol for a parallel-group randomized controlled trial.

Kelly H M Cooijmans, Roseriet Beijers, Anne C Rovers, Carolina de Weerth

Registry-linked trialAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in BMC pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04425096 (The Effect of Skin to Skin Contact on Postpartum Hemorrhage, Pain And Breastfeeding), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04425096 nacompletednot on this mapstarted 2020, after this paper: background citation

The Effect of Skin to Skin Contact on Postpartum Hemorrhage, Pain And Breastfeeding: Randomized Controlled Trial

TypeinterventionalSponsorSaglik Bilimleri UniversitesiRan2020 to 2020Enrolled64ConditionsSkin to Skin ContactArmsSkin to skin contact
3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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  17. Birth Experience, Postpartum PTSD and Depression before and during the Pandemic of COVID-19 in Russia.International journal of environmental research and public health · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Kelly H M CooijmansDepartment of Developmental Psychology, Behavioural Science Institute, Radboud University, P.O. Box 9140, 6500 HE, Nijmegen, The Netherlands. k.cooijmans@psych.ru.nl.
Roseriet BeijersDepartment of Developmental Psychology, Behavioural Science Institute, Radboud University, P.O. Box 9140, 6500 HE, Nijmegen, The Netherlands.
Anne C RoversDepartment of Developmental Psychology, Behavioural Science Institute, Radboud University, P.O. Box 9140, 6500 HE, Nijmegen, The Netherlands.
Carolina de WeerthDepartment of Developmental Psychology, Behavioural Science Institute, Radboud University, P.O. Box 9140, 6500 HE, Nijmegen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTwenty-to-forty percent of women experience postpartum depressive symptoms, which can affect both the mother and infant. In preterm infants, daily skin-to-skin contact (SSC) between the mother and her infant has been shown to decrease maternal postpartum depressive symptoms. In full-term infants, only two studies investigated SSC effects on maternal depressive symptoms and found similar results. Research in preterm infants also showed that SSC improves other mental and physical health outcomes of the mother and the infant, and improves the quality of mother-infant relationship. This randomized controlled trial will investigate the effects of a SSC intervention on maternal postpartum depressive symptoms and additional outcomes in mothers and their full-term infants. Moreover, two potential underlying mechanisms for the relation between SSC and the maternal and infant outcomes will be examined, namely maternal oxytocin concentrations and infant intestinal microbiota. METHODS/

designDesign: A parallel-group randomized controlled trial.

participants116 mothers and their full-term infants.

interventionMothers in the SSC condition will be requested to provide daily at least one continuous hour of SSC to their infant. The intervention starts immediately after birth and lasts for 5 weeks. Mothers in the control condition will not be requested to provide SSC. Maternal and infant outcomes will be measured at 2 weeks, 5 weeks, 12 weeks and 1 year after birth. PRIMARY OUTCOME: maternal postpartum depressive symptoms. Secondary maternal outcomes: mental health (anxiety, stress, traumatic stress following child birth, sleep quality), physical health (physical recovery from the delivery, health, breastfeeding, physiological stress), mother-infant relationship (mother-infant bond, quality of maternal caregiving behavior). Secondary infant outcomes: behavior (fussing and crying, sleep quality), physical health (growth and health, physiological stress), general development (regulation capacities, social-emotional capacities, language, cognitive and motor capacities). Secondary underlying mechanisms: maternal oxytocin concentrations, infant intestinal microbiota. DISCUSSION: As a simple and cost-effective intervention, SSC may benefit both the mother and her full-term infant in the short-and long-term. Additionally, if SSC is shown to be effective in low-risk mother-infant dyads, then thought could be given to developing programs in high-risk samples and using SSC in a preventive manner.

trial registrationNTR5697 ; Registered on March 13, 2016.

Indexed as

BiomarkersChild DevelopmentClinical ProtocolsDepression, PostpartumFemaleFollow-Up StudiesGastrointestinal MicrobiomeHumansInfant BehaviorInfant, NewbornKangaroo-Mother Care MethodMaleMother-Child RelationsOxytocinTreatment OutcomeBiomarkersOxytocinFull-term infantsInfant behaviorMental healthMother-infant relationshipPhysical healthPostpartum depressive symptomsRandomized controlled trialSkin-to-skin contact

Identifiers

PMID28683833
PMCPMC5501342

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.