Evidence map›Paper›PMID 42789043›Full record

Observational studyJournal of patient-reported outcomes2026

The QOLA study: psychometric validation of the Quality of Life of Parents of Children with Achondroplasia (QOLA) questionnaire - a multinational study in Germany, Italy, and Portugal.

Adekunle Adedeji, Stefanie Witt, Lea Maric, Maria Salomao, Florian Innig, Inês Alves, Chiara Provasi, Marco Sessa, Klaus Mohnike, Julia Quitmann

Abstract readMulticenter StudyValidation StudyObservational Study
In one paragraph

Observational study in Journal of patient-reported outcomes, 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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0cells of the map it votes in
0citing 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.

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

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

10 authors.

Adekunle AdedejiFaculty of Social Work and Early Childhood Education, HAW Hamburg, Hamburg, Germany. adekunle.adedeji@haw-hamburg.de.ORCID https://orcid.org/0000-0003-4828-1529
Stefanie WittFaculty of Social Work and Early Childhood Education, HAW Hamburg, Hamburg, Germany. Stefanie.Witt@haw-hamburg.de.ORCID https://orcid.org/0000-0002-6143-7594
Lea MaricFaculty of Social Work and Early Childhood Education, HAW Hamburg, Hamburg, Germany.
Maria SalomaoFaculty of Social Work and Early Childhood Education, HAW Hamburg, Hamburg, Germany.
Florian InnigFederal Association for People of Short Stature and their Families (Bundesverband Kleinwüchsige Menschen und ihre Familien e.V.), Bremen, Germany.
Inês AlvesNational Patient Organisation for Skeletal Dysplasias - ANDO, Évora, Portugal.
Chiara ProvasiItalian Association on Achondroplasia (Associazione per l Informazione e lo studio dell acondroplasia) AISAC, Milan, Italy.
Marco SessaItalian Association on Achondroplasia (Associazione per l Informazione e lo studio dell acondroplasia) AISAC, Milan, Italy.
Klaus MohnikeChildren s Hospital, Otto-von-Guericke-Universität Magdeburg, Magdeburg, Germany.ORCID https://orcid.org/0000-0001-5113-8657
Julia QuitmannFaculty of Social Work and Early Childhood Education, HAW Hamburg, Hamburg, Germany. julia.quitmann@haw-hamburg.de.ORCID https://orcid.org/0000-0002-0876-4211

Funding

BioMarin Pharmaceutical BioMarin Pharmaceutical
6 · The paper itself

Abstract

backgroundParents of children with achondroplasia experience multidimensional impacts on quality of life (QoL), yet validated condition-specific instruments for assessing these outcomes across countries are scarce. This study evaluated the psychometric properties of the Quality of Life of Parents of Children with Achondroplasia (QOLA) questionnaire in three European settings.

methodsA multinational, multicentre observational psychometric validation study was conducted in Germany, Italy, and Portugal. Parents/primary caregivers (N = 149) completed the 43-item QOLA (eight conceptual domains) and the EUROHIS-QOL-8 at baseline (T1); a subsample completed follow-up assessments (T2; n = 77) for test-retest analyses. Data quality (missingness, floor/ceiling effects), internal consistency (Cronbach's α; composite reliability), temporal stability (Pearson correlations; intraclass correlation coefficients), and convergent validity (correlations with EUROHIS-QOL-8) were examined. Exploratory factor analysis informed item reduction and domain aggregation, followed by confirmatory factor analysis of the reduced model.

resultsItem-level missingness was minimal, and no substantial floor/ceiling effects were observed. Eight-domain scores showed acceptable to excellent internal consistency (α = 0.706-0.905) and moderate-to-good temporal stability (single-measure ICCs = 0.64-0.75). Convergent validity was supported by negative associations between QOLA domains and generic QoL (r = .15-0.69). Exploratory and confirmatory analyses supported a parsimonious three-factor, 20-item model, comprising Healthcare System Trust, Caregiving Burden and Daily Impact, and Worries About the Future and Social Relationships, with acceptable fit (CFI = 0.935, TLI = 0.925, RMSEA = 0.066), strong reliability (α = 0.852-0.918; CR = 0.864-0.914), and good test-retest stability (r = .670-0.782; average-measure ICCs = 0.801-0.877).

conclusionsThe QOLA demonstrates robust reliability and validity across three countries and offers both an eight-domain profile and a three-factor summary for assessing parental QoL in achondroplasia.

Indexed as

AchondroplasiaParentsQuality of LifeAdolescentAdultChildChild, PreschoolFemaleGermanyHumansItalyMalePortugalPsychometricsReproducibility of ResultsSurveys and QuestionnairesAchondroplasiaCaregiver quality of lifeCross-national studyPatient-reported outcomesPsychometric validation

Identifiers

PMID42789043
PMCPMC13615216

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.