Evidence map›Paper›PMID 41747213›Full record

ArticleJMIR research protocols2026

Implementing an eHealth Model of Care for Pediatric Patients and Families at the End of Treatment for Acute Lymphoblastic Leukemia (EMERGE): Type 2 Nonrandomized Hybrid Implementation-Effectiveness Trial Study Protocol.

Maria C McCarthy, Chris Williams, Michelle Tennant, Richard De Abreu Lourenco, Hannah Pring, Katie Moore, Jane Templeton, Ken Knight, Peter Downie, Stephen Hearps 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. Not yet cited in PubMed.

0numbers the graph read from it
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

11 authors.

Maria C McCarthyClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0000-0001-6543-3921
Chris WilliamsClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0009-0006-6142-6541
Michelle TennantClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0000-0003-4670-2115
Richard De Abreu LourencoCentre for Health Economics Research and Evaluation, University of Technology, Sydney, Australia.ORCID 0000-0002-5978-8774
Hannah PringClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0009-0004-2493-9319
Katie MooreClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0009-0004-5302-7271
Jane TempletonClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0009-0009-2482-6230
Ken KnightClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0000-0002-2005-7237
Peter DownieVictorian Paediatric Integrated Cancer Service, Parkville, Australia.ORCID 0000-0002-2017-9007
Stephen HearpsClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0000-0003-2984-1172
Cinzia De LucaClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, 3052, Australia, 61 93456866.ORCID 0000-0002-9310-1833

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite increasing survival rates for childhood cancers, physical and psychological late effects are common. The end-of-treatment period is recognized as a complex transition period, and there are few evidence-based models of care to address patient and family needs during this early survivorship period. The EMERGE model of care has been developed to provide eHealth-delivered, multidisciplinary care to patients and families in the 12 months following treatment for acute lymphoblastic leukemia, the most common type of pediatric cancer. Objective: The primary aim of this study is to assess the implementation success of the EMERGE model of care into the clinical setting. Secondary aims include evaluating effectiveness and cost consequences. Methods: The study uses a nonrandomized hybrid implementation-effectiveness design, assessing both implementation and clinical outcomes. Implementation metrics include evaluating the reach, acceptability, feasibility, and maintenance of the EMERGE model. Clinical effectiveness outcomes include parent satisfaction with the EMERGE intervention and pre-post intervention evaluation of parent psychological stress and unmet information needs. The Reach, Effectiveness, Adoption, Implementation, and Maintenance implementation science framework was used to guide study outcomes. Semistructured interviews with clinicians and parents will further evaluate the acceptability and sustainability of the EMERGE model and appraise barriers and facilitators to implementation. Cost analysis will include evaluation of the resources required for program delivery and the impact on subsequent health care service use measured using Medicare data and health service usage collected during the EMERGE intervention. Results: The trial commenced in December 2022, and recruitment concluded in October 2025, with 81 families recruited. Data collection is ongoing and is anticipated to be completed in Summer 2026. Conclusions: This study will address a critical gap in multidisciplinary care delivery at the end of treatment for young survivors of acute lymphoblastic leukemia and their families. The EMERGE model has the potential to improve the quality of life of patients and families by providing an early survivorship intervention. Importantly, the usage of an eHealth (telehealth) model will enable distance-delivered care, facilitating family participation regardless of geography. By measuring implementation, clinical, and cost impacts, this study will inform the future development of end-of-treatment models of care that are almost universally lacking in pediatric oncology care.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaTelemedicineTerminal CareChildChild, PreschoolCost-Benefit AnalysisFemaleHumansPediatricschildhood cancere-healthend-of-treatmentinterventionmodel of caretelehealth

Identifiers

PMID41747213
PMCPMC12945096

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.