Evidence map›Paper›PMID 36621525›Full record

ArticleBJPsych open2023

The impact of patient involvement on participant opinions of information sheets.

Georgie Hudson, Sonja M Jansli, Daniel Morris, Til Wykes, Sagar Jilka

Abstract read
In one paragraph

Article in BJPsych open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Unpacking the Impact and Experience of Working With Lived Experience Partners in Mental Health Research-Exploring Research Team and Public Partner Perspectives.Health expectations : an international journal of public participation in health care and health policy · 2026
    Article
  2. Article
  3. Article
  4. Review
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

5 authors.

Georgie HudsonInstitute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; South London and Maudsley NHS Foundation Trust, London, UK; and Division of Psychology and Language Sciences, University College London, London, UK.ORCID https://orcid.org/0000-0002-5002-4890
Sonja M JansliInstitute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; and South London and Maudsley NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0002-1694-8328
Daniel MorrisInstitute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.ORCID https://orcid.org/0000-0001-5118-7344
Til WykesInstitute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; and South London and Maudsley NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0002-5881-8003
Sagar JilkaInstitute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK; South London and Maudsley NHS Foundation Trust, London, UK; and Warwick Medical School, University of Warwick, Coventry, UK.ORCID https://orcid.org/0000-0003-1578-9350

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatient and public involvement (PPI) groups can provide valuable input to create more accessible study documents with less jargon. However, we don't know whether this procedure improves accessibility for potential participants.

aimsWe assessed whether participant information sheets were rated as more accessible after PPI review and which aspects of information sheets and study design were important to mental health patients compared with a control group with no mental health service use.

methodThis was a double-blind quasi-experimental study using a mixed-methods explanatory design. Patients and control participants quantitatively rated pre- and post-review documents. Semi-structured interviews were thematically analysed to gain qualitative feedback on opinions of information sheets and studies. Two-way multivariate analysis of variance was used to detect differences in ratings between pre- and post-review documents.

resultsWe found no significant (

conclusionsResearchers should be aware of what participants want to know about so they can create information sheets addressing these priorities, for example, explaining why the research is necessary. PPI is poorly understood by the wider population and efforts must be made to increase diversity in participation.

Indexed as

accessibilityConsent and capacityinformation sheetspatient and public involvementreadability

Identifiers

PMID36621525
PMCPMC9885327

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.