Evidence map›Paper›PMID 42732898›Full record

ArticleJapan journal of nursing science : JJNS2026

Support for Disclosure of Hereditary Tumor Risk to Children and Adolescents: A Scoping Review.

Kaito Sugima, Naoko Arimori, Mayumi Uchimura, Ai Miyauchi, Shigeko Horiuchi

Abstract readScoping Review
In one paragraph

Article in Japan journal of nursing science : JJNS, 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

5 authors.

Kaito SugimaGraduate School of Health Sciences, Niigata University, Niigata, Japan.ORCID https://orcid.org/0009-0003-4230-5822
Naoko ArimoriGraduate School of Health Sciences, Niigata University, Niigata, Japan.ORCID https://orcid.org/0000-0002-1144-9669
Mayumi UchimuraGraduate School of Nursing Science, St. Luke's International University, Tokyo, Japan.ORCID https://orcid.org/0009-0000-8921-9196
Ai MiyauchiGraduate School of Nursing Science, St. Luke's International University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3815-8642
Shigeko HoriuchiGraduate School of Nursing Science, St. Luke's International University, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7412-3941

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThis study aimed to map evidence on disclosure support for communicating hereditary tumor-related information to children and adolescents and identify evidence gaps.

methodsThis scoping review was conducted in accordance with the Joanna Briggs Institute methodology and reported in accordance with PRISMA-ScR. Guided by the Population-Concept-Context framework, we identified literature addressing support for disclosing hereditary tumor-related information to children aged ≤ 18 years. PubMed, MEDLINE, CINAHL, and the Cochrane Library were searched through April 2025, without language or study design restrictions. Data were charted and synthesized according to resource characteristics, support content, theoretical foundations, and evaluation approaches.

resultsTen studies described eight resources, including booklets, picture books, decision-support tools, educational programs, and a multiple-family discussion group. Most resources focused on elementary school-aged children and emphasized parent-led disclosure. Common content included basic genetic concepts, disease and inherited risk information, and surveillance or preventive measures. In contrast, psychosocial elements were less consistently incorporated. Only three studies evaluated disclosure support (i.e., one randomized controlled trial, one pre-post study, and one qualitative study). Reported theoretical foundations included the Ottawa Decision Support Framework, health behavior change theories, bibliotherapy, and cognitive developmental theory.

conclusionsOnly a small number of resources have been empirically evaluated, and psychosocial components were not consistently described or explicitly incorporated. Developmentally appropriate, theory-informed approaches-particularly decision-support and bibliotherapy-based resources-may help families engage in informed disclosure and build shared understanding. Future research should develop, implement, and rigorously evaluate structured interventions suitable for routine clinical practice, in collaboration with children, parents, and healthcare professionals.

Indexed as

DisclosureGenetic Predisposition to DiseaseNeoplasmsAdolescentChildHumans

Identifiers

PMID42732898
PMCPMC13571896

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.