Evidence map›Paper›PMID 31018847›Full record

ArticleBMC pediatrics2019

Measuring social participation in children with chronic health conditions: validation and reference values of the child and adolescent scale of participation (CASP) in the German context.

Freia De Bock, Catherin Bosle, Christine Graef, Johannes Oepen, Heike Philippi, Michael S Urschitz

Abstract readMulticenter Study
In one paragraph

Article in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

6 authors.

Freia De BockDivision of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology und Informatics, University Medical Centre of the Johannes Gutenberg-University, Langenbeckstraße 1, 55101, Mainz, Germany. Freia.debock@medma.uni-heidelberg.de.ORCID 0000-0002-7089-8106
Catherin BosleMannheim Institute of Public Health, Social and Preventive Medicine, University Medicine Mannheim, Heidelberg University, Ludolf-Krehl Strasse 7-11, 68167, Mannheim, Germany.
Christine GraefDivision of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology und Informatics, University Medical Centre of the Johannes Gutenberg-University, Langenbeckstraße 1, 55101, Mainz, Germany.
Johannes OepenKlinik Viktoriastift, Cecilienhöhe 3, 55543, Bad Kreuznach, Germany.
Heike PhilippiCenter for Child Neurology, Frankfurt-Mitte, Theobald-Christ-Str. 16, 60316, Frankfurt am Main, Germany.
Michael S UrschitzDivision of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology und Informatics, University Medical Centre of the Johannes Gutenberg-University, Langenbeckstraße 1, 55101, Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile ICF-CY-based models of care are promising avenues for improving participation of children with chronic health conditions, feasible and valid instruments to assess participation as an outcome in routine are still needed. We aimed to validate a German parent-report version of the Child and Adolescent Scale of Participation (CASP) in children with chronic health conditions of different severity.

methodsCross-sectional data were collected in 327 children (mean age 7.8 years, 55% boys) from two paediatric centres (n = 112) and one population-based sample (n = 215). Cronbach's alpha, factor analyses, face validity assessments, correlation analyses, receiver operating characteristics (ROC) curves, and parent-reported health-related quality of life (HRQoL: KINDL) were used to examine internal consistency, test-retest reliability, and capacity to differentiate between disease severity groups. Disease severity was operationalized according to ICD-diagnosis groups and/or parent-reports on health problems, medical and educational support, and medication. A newly developed item "overall perceived participation" was added to the CASP and evaluated.

resultsWe found good to excellent content validity, excellent internal consistency, and good-to-excellent test-retest reliability of the instrument. While children with mild disease had a significantly greater extent of participation (higher CASP scores) than children with severe disease, they did not differ from healthy children. Children with mild compared to severe disease much more differed in participation as measured by the CASP compared to the KINDL (area under the ROC curve: 0.92 vs. 0.75). In addition, the item "overall perceived participation" was highly correlated (r = 0.86) with the CASP total score, indicating the potential value of this specific single item. Finally, we provided preliminary reference values for the CASP obtained in a population-based sample of children without chronic health conditions.

conclusionsThe German version of the CASP and the new item are efficient, valid and reliable measures of social participation in childhood. The CASP-measured participation focuses more on attendance than on involvement into social circumstances of everyday life. To detect children with a high burden of disease on everyday life, the CASP may be more accurate than HRQoL instruments such as the KINDL. As outcome measurement, the CASP may facilitate the implementation of patient-centred paediatric health care.

Indexed as

Quality of LifeAdolescentAge FactorsChildChild, PreschoolChildren with DisabilitiesChronic DiseaseCross-Sectional StudiesFactor Analysis, StatisticalFemaleGermanyHumansMalePsychometricsReference ValuesReproducibility of ResultsChildrenChronic health conditionPsychometric evaluationQuality of lifeSocial participationValidation

Identifiers

PMID31018847
PMCPMC6482577

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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.