Evidence map›Paper›PMID 40711690›Full record

ArticleJournal of patient-reported outcomes2025

Development of the QoLISSY 0-4 questionnaire: a health-related quality of life tool for young children with short stature.

Adekunle Adedeji, Stefanie Witt, Julia Quitmann

Abstract read
In one paragraph

Article in Journal of patient-reported outcomes, 2025. 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
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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

The trial behind 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

3 authors.

Adekunle AdedejiDepartment of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany. Adekunle.adedeji@haw-hamburg.de.ORCID http://orcid.org/0000-0003-4828-1529
Stefanie WittDepartment of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany.
Julia QuitmannDepartment of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Short stature in children aged 0-4 years presents unique physical, social, and emotional challenges that significantly impact health-related quality of life (HRQoL). The QoLISSY 0-4 questionnaire was developed as a Patient Reported Outcome measure (PROMS) to address the absence of an age-specific, condition-focused HRQoL assessment tool for this population. A mixed-method approach was employed to adapt the original QoLISSY questionnaire for children aged 5-18. Qualitative interviews were conducted with 24 parents of children diagnosed with short-stature conditions, including achondroplasia, small for gestational age, growth hormone deficiency, and Silver-Russell Syndrome. Cognitive debriefing sessions and iterative feedback guided the development of new items tailored to the needs of children aged 0-4. Pilot testing involved 20 parents, who evaluated the questionnaire's clarity, relevance, and comprehensiveness. The development process yielded an 8-domain, 55-item questionnaire addressing physical health, social interactions, emotions, coping mechanisms, medical care, future concerns, and parental impact. Cognitive debriefing results indicated high item clarity (100%), relevance (93%), and importance (94%), with parents confirming that the questionnaire effectively captured their child's HRQoL experiences. The QoLISSY 0-4 questionnaire provides a tailored, parent-reported tool for assessing HRQoL in children aged 0-4 with short stature. Its development reflects a rigorous, participant-informed process ensuring its relevance and usability. Future validation studies will explore its cross-cultural applicability and psychometric properties to establish its utility in research and clinical settings.

Indexed as

DwarfismPatient Reported Outcome MeasuresQuality of LifeAdolescentChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleParentsPsychometricsSurveys and QuestionnairesCognitive debriefingEarly childhood healthHealth-related quality of life (HRQoL)Pediatric assessmentPROMsQOLISSYQuestionnaire developmentShort stature

Identifiers

PMID40711690
PMCPMC12297059

What OpenQuestion holds

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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.