Evidence map›Paper›PMID 42726101›Full record

ArticleRheumatology (Oxford, England)2026

Online peer support in rheumatology: a mixed methods exploration of patient and clinician views and experiences.

Shihab Ahmed, Martha Piper, Michael Bosley, Shaista Tayabali, Alice Tunks, Sean Humfrey, Wendy Diment, Max Yates, James A Bourgeois, Melanie Sloan

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

10 authors.

Shihab AhmedSchool of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID 0009-0003-2642-2949
Martha PiperDepartment of Public Health and Primary Care Unit, University of Cambridge, Cambridge, UK.
Michael BosleyPatient and Public Partner.
Shaista TayabaliPatient and Public Partner.
Alice TunksDepartment of Public Health and Primary Care Unit, University of Cambridge, Cambridge, UK.
Sean HumfreyPatient and Public Partner.
Wendy DimentPatient and Public Partner.
Max YatesFaculty of Medicine and Health Sciences, University of East Anglia, Norwich, UK.ORCID 0000-0003-3977-8920
James A BourgeoisDepartment of Psychiatry and Behavioral Sciences, University of California, Davis Medical Center, Sacramento, CA, USA.
Melanie SloanDepartment of Public Health and Primary Care Unit, University of Cambridge, Cambridge, UK.

Funding

Lupus UK and The Lupus Trust
6 · The paper itself

Abstract

objectivesOnline peer support groups (OSGs) are increasingly used by patients with rheumatic diseases, yet their benefits, risks and impact on the clinician-patient relationship are not well characterized. We examined how patients and clinicians perceive and experience OSGs.

methodsMixed methods combining online surveys and interviews with rheumatology patients and clinicians. Measures of satisfaction with life and care were compared by t-tests between OSG members and non-members. Free-text and interview data underwent thematic analysis.

resultsThree themes were identified from surveys (n = 1316 patients, n = 317 clinicians) and interviews (n = 19 patients, n = 14 clinicians). (1) Validation and affirmation: OSGs provided emotional reassurance, understanding and belonging, especially those with rare or 'invisible' diseases who felt disbelieved by others. (2) Patient empowerment through health literacy: OSGs filled informational and relational gaps left by time-limited healthcare systems, offering practical, experience-based advice. Although 85% of patients reported finding helpful information on OSGs, 48% reported misinformation circulating in groups. Effective moderation was viewed as key. (3) Tensions and inequities within peer spaces: 71% of clinicians viewed OSGs as helpful, while many worried about negativity and distrust in healthcare systems. Members described 'toxic positivity', 'toxic negativity' and exclusionary dynamics within the OSGs, with younger, male and racially minoritized patients more likely to report feeling unwelcome.

conclusionOSGs can offer meaningful emotional and practical benefits to patients with rheumatic diseases, particularly those who feel marginalized in social or clinical contexts. However, these benefits coexist with challenges around misinformation, inclusivity and the clinician-patient relationship.

Indexed as

Attitude of Health PersonnelPeer GroupRheumatic DiseasesRheumatologySelf-Help GroupsSocial SupportAdultAgedFemaleHealth LiteracyHumansMaleMiddle AgedPatient SatisfactionPhysician-Patient RelationsRheumatologistsattitude of health professionalsmental health servicesmixed methodspatient attitude to healthpatient experienceprimary care rheumatologyRASjogren’s syndromeSLEsocial support

Identifiers

PMID42726101
PMCPMC13630447

What OpenQuestion holds

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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.