Evidence map›Paper›PMID 42341234›Full record

ArticleJMIR research protocols2026

Adaptation of the Transition Readiness Assessment Questionnaire for Pediatric-Onset Multiple Sclerosis: Protocol for a User-Centered Design Approach.

Claudia Gambrah-Lyles, Aaron W Abrams, Sara Loud, Hollie Schmidt, Emily Blosberg, Melissa Wright, Kelsey E Poisson, Kristen S Fisher, Kimberly A O'Neill, Akash Virupakshaiah and 1 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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. Review
4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Claudia Gambrah-LylesDepartment of Neurology, School of Medicine, Washington University in St. Louis, 1 Children's Place, St. Louis, MO, 63110, United States, 1 314 471 2986.ORCID 0000-0002-2448-2265
Aaron W AbramsDepartment of Neurology, Center for Pediatric Neurosciences and Mellen Center for MS Treatment and Research, Cleveland Clinic Neurological Institute, Cleveland, OH, United States.ORCID 0000-0002-4607-5740
Sara LoudAccelerated Cure Project for Multiple Sclerosis, Waltham, MA, United States.ORCID 0009-0002-1060-8960
Hollie SchmidtAccelerated Cure Project for Multiple Sclerosis, Waltham, MA, United States.ORCID 0000-0003-4467-7374
Emily BlosbergMr Oscar Monkey, Elk Mound, WI, United States.ORCID 0009-0002-4645-051X
Melissa WrightDepartment of Neurology, Division of Pediatric Neurology, University of Utah School of Medicine, Salt Lake City, UT, United States.ORCID 0000-0002-7804-9627
Kelsey E PoissonDepartment of Pediatrics, Division of Neurology, Nationwide Children's Hospital, Columbus, OH, United States.ORCID 0000-0003-3557-0532
Kristen S FisherDepartment of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, United States.ORCID 0000-0002-1598-8571
Kimberly A O'NeillDepartment of Neurology, NYU Grossman School of Medicine, New York, NY, United States.ORCID 0000-0001-6021-8683
Akash VirupakshaiahDepartment of Neurology, Divisions of Pediatric Neurology and Neuroimmunology & Glial Biology, Weill Institute for Neurosciences University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0003-2624-9974
John W RoseDepartment of Neurology, University of Utah School of Medicine, Salt Lake City, UT, United States.ORCID 0000-0003-2382-5921

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pediatric-onset multiple sclerosis (POMS) is a chronic, progressive neurologic condition requiring lifelong management and coordinated transition from pediatric to adult care. Evidence-based guidelines identify transition readiness assessment as a core component of successful transition; however, most POMS clinics do not formally assess readiness, and existing tools do not address POMS-specific challenges, such as fluctuating disability, complex treatment regimens, and cognitive impairment. This gap underscores the need for a transition readiness measure tailored to POMS. Objective: This paper aims to describe a stakeholder-engaged, implementation science-guided protocol for adapting the Transition Readiness Assessment Questionnaire (TRAQ) version 6.0 to reflect the unique developmental and clinical needs of youth with POMS. Methods: Using adaptation and participatory research as our guiding implementation strategies, surveys will be administered to patients, caregivers, and clinicians to identify barriers to and facilitators of transition to adult care and define essential self-management competencies in POMS. Survey content will be informed by constructs from the dynamic adaptation process framework and existing TRAQ 6.0 domains. Identified competencies will be refined using a Delphi consensus process. Through cognitive interviewing and a multidisciplinary focus group of collaborators, the adapted measure will be reviewed to assess clarity, relevance, and perceived clinical utility. Results: This project will generate a consensus-driven set of POMS-specific transition competencies and systematically adapt the TRAQ 6.0 to the POMS population. This study was funded in July 2025. The health care provider survey was disseminated in November 2025 across the 27 sites in the US Network of Pediatric Multiple Sclerosis Centers. The patient and caregiver surveys have been finalized, and distribution is projected to begin in June 2026, with a target of 15 patients and 15 caregivers. As of manuscript submission, no patients or caregivers have been recruited, and data analysis has not yet started. Data collection is expected to conclude by the end of 2026, and results are anticipated for publication in 2027. Conclusions: This protocol outlines a rigorous, replicable approach to adapting a validated transition readiness measure to POMS. The adapted TRAQ 6.0 will support evidence-based transition planning and inform future psychometric testing and implementation research to improve the care of patients with POMS as they age.

Indexed as

Multiple SclerosisTransition to Adult CareUser-Centered DesignAdolescentChildHumansImplementation SciencePsychometricsSurveys and Questionnairesadaptationimplementation sciencemultiple sclerosisparticipatory researchpediatric-onset multiple sclerosistransition to adult care

Identifiers

PMID42341234
PMCPMC13293475

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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.