Evidence map›Paper›PMID 29146642›Full record

ArticleBMJ open2017

'When it goes back to my normal I suppose': a qualitative study using online focus groups to explore perceptions of 'control' among people with eczema and parents of children with eczema in the UK.

Laura M Howells, Joanne R Chalmers, Fiona Cowdell, Sonia Ratib, Miriam Santer, Kim S Thomas

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% of its field
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  5. Patient and Public Involvement in Dermatology Research: A Review.American journal of clinical dermatology · 2022
    Review
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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

6 authors at 3 institutions in 1 country.

Laura M HowellsCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.ORCID http://orcid.org/0000-0003-4157-7394
Joanne R ChalmersCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Fiona CowdellFaculty of Health Education and Life Sciences, Birmingham City University, Birmingham, UK.
Sonia RatibCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Miriam SanterPrimary Care and Population Sciences, University of Southampton, Southampton, UK.ORCID http://orcid.org/0000-0001-7264-5260
Kim S ThomasCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.ORCID http://orcid.org/0000-0001-7785-7465
University of Nottingham · GBBirmingham City University · GBUniversity of Southampton · GB

Funding

Department of Health PDF-2009-02-45
6 · The paper itself

Abstract

objectiveTo inform the development of a core outcome set for eczema by engaging with people with eczema and parents of children with eczema to understand their experiences and understanding of the concept 'eczema control'.

design37 participants took part in a total of six semi-structured online focus groups held in a typed chatroom with 5-7 participants per group. Three groups involved adults with eczema and three groups involved parents of children with eczema. Framework analysis was used for data analysis.

settingA community-based sample was recruited from across the UK via social media and email.

participants19 adults aged 17-61 years (15/19 female, 16/19 white) and 18 parents of children with eczema aged 9 months-17 years (9/18 female, 18/19 white).

resultsFour main themes were identified:(1) 'Commonalities and differences in the experiences of control': a reduction in symptoms such as itch and sleep loss characterised eczema control, but what level was acceptable differed across participants;(2) 'Eczema control goes beyond the skin': psychological factors, social factors, the constant scratching and the impact on everyday activities are a variety of ways an individual can be impacted;(3) 'Stepping up and down of treatment': participants' stepped-up treatment in response to loss of control, but several factors complicated this behaviour. Control needed to be maintained after stepped-up treatment ended to be acceptable; and (4) 'How to measure control': self-report was generally preferred to allow frequent measurements and to capture unobservable features. Although most thought their eczema needed to be measured frequently, many also felt that this was not always realistic or desirable.

conclusions'Eczema control' is a complex experience for people with eczema and parents of children with the condition. These experiences could have important implications on how long-term control should be measured in eczema clinical trials and clinical practice.

Indexed as

Disease ManagementAdolescentAdultChildChild, PreschoolEczemaFemaleFocus GroupsHumansInfantMaleMiddle AgedParentsQualitative ResearchSelf ReportUnited Kingdomdermatologyeczemaqualitative research

Identifiers

PMID29146642
PMCPMC5695402
OpenAlexW2762211612

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.