Evidence map›Paper›PMID 41407410›Full record

ArticleBMJ open2025

Chronic illness experiences for young adults: a qualitative study.

Imogen Harper, Alex Broom, Louise Baur, Emmanuel Stamatakis

Abstract read
In one paragraph

Article in BMJ open, 2025. 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

4 authors.

Imogen HarperSydney Centre for Healthy Societies, Faculty of Arts and Social Sciences, The University of Sydney, Sydney, New South Wales, Australia imogen.harper@sydney.edu.au.ORCID http://orcid.org/0000-0002-3019-5123
Alex BroomSydney Centre for Healthy Societies, Faculty of Arts and Social Sciences, The University of Sydney, Sydney, New South Wales, Australia.
Louise BaurSydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
Emmanuel StamatakisMackenzie Wearables Research Hub, Charles Perkins Centre, The University of Sydney, Sydney, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo explore the experience and impact of physical chronic illnesses in the lives of young people.

designQualitative study using semi-structured interviews.

settingInterviews were conducted between March 2023 and February 2024 either via video call (14) or face-to-face (19). Recruitment was done primarily through flyers in public spaces, specialists' waiting rooms and research pages of chronic disease websites and supplemented through snowballing.

participantsYoung adults aged 19-29 years (n=33, mean age 23 years) who had lived with a physical chronic illness for 6 months or more. All participants lived in Australia.

resultsThree key findings were identified: (i) chronic illness impacts the lives of young people in a particular way, as participants reported that their young age, and the youth of their peers, influenced their interactions with healthcare professionals, their access to support and their sense of isolation; (ii) participants struggled to come to terms with, and describe, the influence of their chronic illness on their overall life and lifestyle, particularly when outside of the 'expected' symptoms of disease; (iii) the lack of education and guidance about the wide range of impacts that chronic illness can have seemed to compound participants' reported sense of guilt, self-blame and exhaustion.

conclusionsThis study illustrates how youth is a critical contextual element when considering different population groups' challenges in managing chronic illnesses. It finds that young people may internalise blame for these challenges despite the fact they are structural issues. Understanding this context will aid the provision of better healthcare experiences and support programmes. Further research could help establish better expert and peer support models to help adults and young people better anticipate, understand and manage the wide-reaching impacts of chronic illness.

Indexed as

Quality of LifeAdultAustraliaChronic DiseaseFemaleHumansInterviews as TopicMaleQualitative ResearchYoung AdultChronic DiseaseQUALITATIVE RESEARCHSelf-Management

Identifiers

PMID41407410
PMCPMC12716523

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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.