Evidence map›Paper›PMID 42097698›Full record

ArticleLupus science & medicine2026

Impact of an online lupus self-management programme in an established, population-based cohort of adults with diagnosed SLE: a mixed-methods study.

Sarah D Gilman, Sara Johnson, Gaobin Bao, Charmayne Marie Dunlop-Thomas, Katherine Carpenter, Melissa French, Cristina Drenkard, Melicent Miller, Mary Crimmings, S Sam Lim

Abstract read
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Article in Lupus science & medicine, 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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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Sarah D Gilman *Wayfinder Health Strategies, Falls Church, Virginia, USA sarahgilman@wayfinderhs.com.ORCID 0000-0002-1885-0017
Sara Johnson *Pro-Change Behavior Systems, Wakefield, Rhode Island, USA.
Gaobin BaoMedicine/Rheumatology, Emory University, Atlanta, Georgia, USA.
Charmayne Marie Dunlop-ThomasMedicine/Rheumatology, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-5770-1583
Katherine CarpenterLupus Foundation of America, Washington, District of Columbia, USA.
Melissa FrenchLupus Foundation of America, Washington, District of Columbia, USA.
Cristina DrenkardMedicine/Rheumatology, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-6832-7291
Melicent MillerLupus Foundation of America, Washington, District of Columbia, USA.
Mary CrimmingsLupus Foundation of America, Washington, District of Columbia, USA.
S Sam LimMedicine/Rheumatology, Emory University, Atlanta, Georgia, USA.ORCID 0000-0003-2361-0787

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveStrategies to Embrace Living with Lupus Fearlessly (SELF) is an online self-management education programme for people with SLE. This mixed-methods study examines SELF's impact on patient-reported outcomes while assessing implementation outcomes informing feasibility and dissemination.

methodsA convergent mixed-methods design was used, merging qualitative and quantitative data to enhance interpretation. The Reach, Effectiveness, Adoption, Implementation and Maintenance evaluation framework was used to evaluate programme feasibility and sustainment potential. Participants were recruited from the Georgians Organized Against Lupus (GOAL) cohort (Georgia).

results221 adults with SLE from the GOAL cohort enrolled in SELF, completing patient-reported assessments at baseline and 90-day follow-up. 12 participants also completed in-depth interviews exploring the impact of the programme. Certain subgroups including black participants (n=193; 95% CI=-1.59 to -0.04), those with high fatigue levels (n=164; 95% CI=-1.85 to -0.11) and participants living below 100% of the federal poverty level (n=74; 95% CI=-3.44 to -0.18) reported significantly lower disease activity at 90-day follow-up after engaging with SELF. High-fatigue participants improved on multiple measures while the low-fatigue group showed unexpected declines that may reflect baseline confounding. Qualitative findings generally supported quantitative results. One exception was self-efficacy in managing medications, which showed a small but significant decrease (mean reduction=-1.38, 95% CI=-2.50 to -0.26, Cohen's d=-0.14). However, qualitative data suggested participants became more aware of skill gaps rather than less capable.

conclusionsSELF showed promising results for reducing disease activity, pain and fatigue among specific subgroups of participants with SLE. Further research should broaden the evaluation of SELF to new geographical settings, broader populations (such as people living with lupus in rural healthcare settings) and further testing for cultural relevance across diverse racial and ethnic groups.

Indexed as

Lupus Erythematosus, SystemicPatient Education as TopicSelf-ManagementAdultCohort StudiesFatigueFeasibility StudiesFemaleHumansInternetMaleMiddle AgedPatient Reported Outcome MeasuresProgram EvaluationQuality of LifeHealth-Related Quality Of LifeLupus Erythematosus, SystemicPatient Reported Outcome Measures

Identifiers

PMID42097698
PMCPMC13157730

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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.