Evidence map›Paper›PMID 41832059›Full record

ArticleDisability and health journal2026

Factors associated with social participation among children with fragile X syndrome.

Maria G Gonzalez, April D Summers, Lisa D Wiggins, Marc A Schweizer, Angela M Thompson-Paul, Sarah C Tinker

Abstract read
In one paragraph

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

0numbers the graph read from it
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0citing papers in PubMed
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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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Maria G GonzalezDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA. Electronic address: tuk1@cdc.gov.
April D SummersDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.
Lisa D WigginsDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.
Marc A SchweizerDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.
Angela M Thompson-PaulDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA; U.S. Public Health Services, Rockville, MD, USA.
Sarah C TinkerDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA.

Funding

Intramural CDC HHS CC999999NCBDD CDC HHS U01 DD000231NCBDD CDC HHS U01 DD001189NCBDD CDC HHS U19 DD000753
6 · The paper itself

Abstract

backgroundSocial participation may increase quality of life for children with disabilities. However, few studies have explored social participation among children with fragile X syndrome (FXS).

objectivesThe objectives of this analysis were to describe social participation among children with FXS, associations with demographic and clinical characteristics, and caregiver-reported barriers to social participation.

methodsChildren with FXS aged 5-17 years were identified using data collected 2011-2021 in the Fragile X Online Registry With Accessible Research Database. Caregivers reported on types of social activities the child was involved in and specific barriers to social participation. Chi-square tests of independence were used to compare distributions by sex and modified Poisson regression was used to estimate unadjusted and adjusted prevalence ratios (aPRs) and 95% confidence intervals (CI).

resultsAmong children with FXS (n = 830), 81.7% participated in at least one social activity; physical (65.8%) and work or volunteer activities (2.0%) were the most and least common. Children with severe to profound intellectual disability (ID; aPR = 0.57, CI = 0.43-0.77) and emotional dysregulation behaviors (aPR = 0.93, CI = 0.87-1.00) were less likely to participate in a social activity relative to children without these characteristics. Demographic and clinical differences were observed for social participation by activity type. Caregivers most often reported behavioral issues (72.2%), time constraints (64.4%), and lack of community resources (64.2%) as barriers to social participation.

conclusionIncreasing adaptive program availability, activity staff training, and respite support services may improve social participation.

Indexed as

Children with DisabilitiesFragile X SyndromeSocial ParticipationAdolescentCaregiversChildChild, PreschoolFemaleHumansIntellectual DisabilityMaleQuality of LifeRegistriesDevelopmental disabilitiesFragile X syndromeSocial participation

Identifiers

PMID41832059
PMCPMC13454921

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LicenceCC BY-NC-ND
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Registered trials

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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.