Evidence map›Paper›PMID 39085897›Full record

ArticleBMC palliative care2024

Social support resources in adolescents and young adults with advanced cancer: a qualitative analysis.

Nancy Lau, Angela Steineck, Casey Walsh, Kaitlyn M Fladeboe, Joyce P Yi-Frazier, Abby R Rosenberg, Krysta Barton

Abstract read
In one paragraph

Article in BMC palliative care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

7 authors.

Nancy LauCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, 1920 Terry Ave, Seattle, WA, 98101, USA. nancy.lau@seattlechildrens.org.ORCID http://orcid.org/0000-0002-2160-5362
Angela SteineckMACC Fund Center for Cancer and Blood Disorders, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, USA.
Casey WalshClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Kaitlyn M FladeboeBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA, USA.
Joyce P Yi-FrazierDepartment of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, Boston, MA, USA.
Abby R RosenbergDepartment of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, Boston, MA, USA.
Krysta BartonBiostatistics Epidemiology and Analytics for Research (BEAR) Core, Seattle Children's Research Institute, Seattle, WA, USA.

Funding

Pilot trial testing mobile health psychosocial intervention for Adolescentsand Young Adults with cancerK08CA263474 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI Nancy Lau · 2022 to 2026
$1.0M
NCI NIH HHS K08 CA263474
6 · The paper itself

Abstract

purposeAdolescents and Young Adults (AYAs) with cancer are an at-risk group with unique palliative and supportive care needs. Social support in AYAs with cancer is associated with better coping, quality of life, and psychosocial well-being. Here, we extend existing research to examine the sources and types of support received by AYAs with advanced cancer.

methodsAYAs participated in a semi-structured, 1:1 interview on communication and psychosocial support needs. The present analysis focused on social support experiences for AYAs with advanced cancer. Directed content analysis was used to develop the codebook. Established social support constructs provided a coding framework. We presented our qualitative findings as a code frequency report with quantified frequency counts of all "source of support" and "type of support" codes. We assigned a global "sufficiency of support code" to each AYA.

resultsWe interviewed 32 AYAs with advanced cancer (Mage = 18, SDage = 3.2, 41% female). Most AYAs identified family (namely, caregivers) as their primary source of support and stated that family universally provided all types of support: emotional, informational, instrumental, and social companionship. They received informational and emotional support from clinicians, and received emotional support and social companionship from healthy peers, cancer peers, and their existing community. One-third of participants were coded as having "mixed support" and described a lack of support in some domains.

conclusionAYAs with advanced cancer described caregivers as their universal source of support, and that other support sources provided support for specific needs. Future research should continue to evaluate social support needs and family-based palliative and supportive care interventions to bolster social support resources in this high-risk group.

Indexed as

NeoplasmsQualitative ResearchSocial SupportAdaptation, PsychologicalAdolescentAdultFemaleHumansMaleQuality of LifeYoung AdultAdolescentsAdvanced cancerPsychosocial support systemsQualitative researchSocial supportYoung adults

Identifiers

PMID39085897
PMCPMC11290203

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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.