Evidence map›Paper›PMID 42319681›Full record

ArticleJournal of patient-reported outcomes2026

Development and pilot testing of the quality of life of parents of children with achondroplasia questionnaire.

Adekunle Adedeji, Stefanie Witt, Maria Salomão, Tabea Steinhoff, Florian Innig, Inês Alves, Chiara Provasi, Marco Sessa, Klaus Mohnike, Julia Quitmann

Abstract read
In one paragraph

Article 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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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 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 Childhood Education, HAW Hamburg, Hamburg, Germany. stefanie.witt@haw-hamburg.de.
Maria SalomãoFaculty of Social Work and Childhood Education, HAW Hamburg, Hamburg, Germany. mariasalomaoue@gmail.com.
Tabea SteinhoffInstitute of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Florian InnigFederal Association for People of Short Stature and their Families (Bundesverband Kleinwüchsige Menschen und ihre Familien e.V.), BKMF, Bremen, Germany.
Inês AlvesNational Association for Skeletal Dysplasias - ANDO Portugal, Evora, 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 University Magdeburg, Magdeburg, Germany.
Julia QuitmannFaculty of Social Work and Childhood Education, HAW Hamburg, Hamburg, Germany. Julia.Quitmann@haw-hamburg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParents of children with achondroplasia face sustained caregiving demands that may affect multiple dimensions of well-being. Despite growing recognition of these challenges, no validated, condition-specific instrument exists to assess the quality of life (QoL) of parents of children with achondroplasia. This study aimed to develop, and pilot test the Quality of Life of Parents of Children with Achondroplasia (QOLA) questionnaire.

methodsQOLA was developed using a multi-phase mixed-methods design in accordance with established standards for developing self-reported outcome measures for caregivers and parents. Phase 1 comprised semi-structured qualitative interviews with 17 parents of children with achondroplasia to identify relevant QoL domains and language. Interview data were analysed using qualitative content analysis and informed systematic item generation (Phase 2). Conceptual structure was examined through researcher-led card sorting (Phase 3) and two rounds of international card sorting following translation (Phase 4). The resulting 63-item questionnaire across eight domains was pilot-tested in a cross-sectional, multi-country study with embedded cognitive debriefing in Germany, Italy, and Portugal (total N = 50).

resultsThe final pilot version of QOLA comprised 63 items across eight domains covering healthcare experiences, challenges and support, physical health, mental health, social life and relationships, coping, family and daily life, and worries and future concerns. Item-level missing data were minimal, and no pronounced floor or ceiling effects were observed. Internal consistency was acceptable to good for domains (α = 0.624-0.821) and good for the total scale (α = 0.798). Inter-domain correlations were generally moderate to strong. Cognitive debriefing was highly acceptable and relevant across countries, with some suggestions for further refinement.

conclusionsQOLA shows strong preliminary evidence of acceptability and internal consistency and addresses a key measurement gap in achondroplasia research. Further large-scale psychometric validation is warranted.

Indexed as

AchondroplasiaCaregiversParentsQuality of LifeAdolescentAdultChildCross-Sectional StudiesFemaleGermanyHumansMaleMiddle AgedPilot ProjectsPortugalPsychometricsAchondroplasiaCaregiver burdenParentsPilot studyQuality of lifeQuestionnaire development

Identifiers

PMID42319681
PMCPMC13282410

What Socratic holds

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LicenceCC BY
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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 Socratic graph.