Evidence map›Paper›PMID 39401060›Full record

ArticleThe American journal of gastroenterology2025

Development and Validation of a Pediatric Celiac Disease-Specific Quality of Life Measure.

Shayna Coburn, Paige J Trojanowski, Jack Vagadori, Pamela Hinds, Monique Germone, Edwin Liu, Randi Streisand, James Bost

Abstract readValidation Study
In one paragraph

Article in The American journal of gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Shayna CoburnCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.ORCID 0000-0001-9526-3580
Paige J TrojanowskiCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.ORCID 0000-0002-4118-9087
Jack VagadoriCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.ORCID 0000-0001-7443-6438
Pamela HindsCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.
Monique GermoneDigestive Health Institute, Children's Hospital Colorado, Aurora, Colorado, USA.ORCID 0000-0001-6827-5551
Edwin LiuDigestive Health Institute, Children's Hospital Colorado, Aurora, Colorado, USA.ORCID 0000-0003-3591-8922
Randi StreisandCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.
James BostCenter for Translational Research, Children's National Hospital, Washington, District of Columbia, USA.

Funding

Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
A behavioral intervention to optimize self-management of celiac disease in adolescentsK23DK129826 · NIDDK · CHILDREN'S RESEARCH INSTITUTE · PI COBURN, SHAYNA SKELLEY · 2021 to 2025
$793k
I-TrainED: Innovative Training and Education in DiabetesK26DK138330 · NIDDK · CHILDREN'S RESEARCH INSTITUTE · PI RANDI STREISAND · 2023 to 2026
$479k
NCATS NIH HHS UL1 TR001876NCATS NIH HHS UL1TR001876 (Pilot Subaward)NIDDK NIH HHS K23 DK129826NIDDK NIH HHS K23DK129826NIDDK NIH HHS K26 DK138330
6 · The paper itself

Abstract

introductionQuality of life (QOL) is critical in screening and management of chronic medical conditions, including celiac disease (CD). The aim of this project was to develop a CD-specific pediatric QOL measure (Celiac Disease Life Inventory of Family Experiences [CDLIFE]) with parallel self-report and parent-report forms by generating items through concept elicitation interviews, iterative refinement using cognitive debriefing interviews, and evaluating its psychometric properties and validity.

methodsConcept elicitation interviews were conducted to develop items (9 youth ages 8-19 years with CD; 10 parents of youth with CD), followed by cognitive interviews with additional stakeholders (3 youth with CD, 3 parents, and 8 clinicians) and item administration (parent/youth reports: n = 103/102). Analyses included response frequencies, internal consistency reliability, exploratory factor analyses, and correlations with related measures (Patient-Reported Outcomes Measurement Information System, Pediatric Quality of Life Inventory, and Gluten-Free Diet-Visual Analog Scale).

resultsFrom concept elicitation interviews, 42 youth and 45 parent items were developed. Cognitive debriefing interviews yielded 36 refined items. Psychometric analyses identified 15 items to remove due to ceiling/floor effects, poor item-to-test correlations, and youth-parent mismatch or conceptual mismatch. Total score internal consistency was high (αs = 0.89-0.90). A 4-factor model solution had the best fit (Social Impact, External Support, Adaptive Vigilance, Eating Behaviors/Adjustment) with a fifth single-item domain (Financial Resources). The final CDLIFE (21 items) total scores correlated with most related measures in expected directions for parent and youth forms. DISCUSSION: The CDLIFE may facilitate insight into CD-specific QOL for youth ages 2-18 years, capturing important dimensions of physical and socioemotional health. Administering the CDLIFE will help identify and track families needing support.

Indexed as

Celiac DiseaseQuality of LifeAdolescentChildDiet, Gluten-FreeFemaleHumansMaleParentsPatient Reported Outcome MeasuresPsychometricsReproducibility of ResultsSelf ReportSurveys and QuestionnairesYoung Adultparentspediatricsurveyyouth

Identifiers

PMID39401060
PMCPMC11994830

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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.