Evidence map›Paper›PMID 42063376›Full record

ArticleChild: care, health and development2026

Caregiver Concerns for Children and Adolescents With Down Syndrome: A Cross-Sectional Study in Brazil.

Beatriz Helena Brugnaro, Henrique Granado Jábali, Rosa Isabel Fonseca Angulo, Rafaela Campos, Marilyn Wright, Rachel Teplicky, Peter Rosenbaum, Olaf Kraus de Camargo, Nelci Adriana Cicuto Ferreira Rocha

Abstract read
In one paragraph

Article in Child: care, health and development, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Beatriz Helena BrugnaroDepartment of Physical Therapy, Child Development Analysis Laboratory (LADI), Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-7883-3123
Henrique Granado JábaliDepartment of Physical Therapy, Child Development Analysis Laboratory (LADI), Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.
Rosa Isabel Fonseca AnguloDepartment of Physical Therapy, Child Development Analysis Laboratory (LADI), Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.
Rafaela CamposDepartment of Physical Therapy, Child Development Analysis Laboratory (LADI), Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.
Marilyn WrightCanChild Centre for Childhood-Onset Disability Research, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0003-2931-5746
Rachel TeplickyCanChild Centre for Childhood-Onset Disability Research, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-8149-4756
Peter RosenbaumCanChild Centre for Childhood-Onset Disability Research, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0001-6751-5613
Olaf Kraus de CamargoCanChild Centre for Childhood-Onset Disability Research, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-7927-7189
Nelci Adriana Cicuto Ferreira RochaDepartment of Physical Therapy, Child Development Analysis Laboratory (LADI), Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil.

Funding

Coordination for the Improvement of Higher Education Personnel (CAPES) 001São Paulo Research Foundation (FAPESP) 2019/13570-6São Paulo Research Foundation (FAPESP) 2019/13716-0São Paulo Research Foundation (FAPESP) 2021/15016-6
6 · The paper itself

Abstract

aimThe aim of this study is to describe and compare areas of concern for caregivers of children and adolescents with Down syndrome across ages and explore how these areas impact their ability to participate in daily activities.

methodsOne hundred and seventeen caregivers of children and adolescents with Down syndrome, aged 0-18, participated and completed the About My Child questionnaire. Descriptive analyses of data from the caregivers were carried out. Individual item scores and the mean scores, standard deviations, median and confidence interval of the total Concern and Impact scores were calculated. Item analyses were carried out across age groups (Kruskal-Wallis test) and between children and adolescent groups (Mann-Whitney Test), aiming to explore concerns and impacts at different ages.

resultsThe lowest mean concern score for an age group was 9.27, and the highest was 12.67, with possible scores from 0 to 19. The lowest mean impact score for an age group was 2.80, and the highest was 3.25, with possible scores from 0 to 4. The items with the highest frequency of concern for most age groups were communication, participation in school and community and behaviour. The biggest impacts on participation were reported for the items concerning the use of arms and hands, sleep and hearing. No differences were found across age groups.

interpretationThis study found that caregivers of children and adolescents with Down syndrome have concerns about their child that, in total, do not change throughout life.

Indexed as

CaregiversDown SyndromeActivities of Daily LivingAdolescentAdultBrazilChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantInfant, NewbornMaleQuality of LifeSurveys and QuestionnairesAbout My ChildconcernsDown syndromefamiliesfunctional concernsparticipation

Identifiers

PMID42063376
PMCPMC13133700

What OpenQuestion holds

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LicenceCC BY
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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.