Evidence map›Paper›PMID 29420196›Full record

ArticleBMJ supportive & palliative care2018

Enhanced patient research participation: a Photovoice study in Blantyre Malawi.

Maya Jane Bates, Jane Ardrey, Treza Mphwatiwa, Stephen Bertel Squire, Louis Willem Niessen

Open access · hybridAbstract read
In one paragraph

Article in BMJ supportive & palliative care, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Participatory research with carers: A systematic review and narrative synthesis.Health expectations : an international journal of public participation in health care and health policy · 2024
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. The burden of global outbreaks: Photos of the daily lives of children with congenital Zika syndrome during the COVID-19 pandemic.Health expectations : an international journal of public participation in health care and health policy · 2023
    Article
  6. Article
  7. Article
  8. Patients as partners in health research: A scoping review.Health expectations : an international journal of public participation in health care and health policy · 2021
    Article
  9. Review
  10. 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

5 authors at 4 institutions in 2 countries.

Maya Jane BatesDepartment of Family Medicine, College of Medicine, Blantyre, Malawi.ORCID http://orcid.org/0000-0002-4459-837X
Jane ArdreyDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Treza MphwatiwaAfrican Network for the Care of Children Affected by HIV and AIDS, College of Medicine, Lilongwe, Malawi.
Stephen Bertel SquireDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Louis Willem NiessenDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Liverpool School of Tropical Medicine · GBChristian Health Association of Malawi · MWUniversity of Liverpool · GBUniversity of Malawi · MW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatient involvement in palliative care research is a desirable if challenging goal. Photovoice is an action research method in which affected communities gather photographs to document and discuss their communities' strengths and concerns. Engagement with policymakers is a separately stated goal. Photovoice is increasingly used in health-related research but has not been widely described in the palliative care literature. We report on experiences and lessons learnt using Photovoice in Blantyre, Malawi to encourage its wider use in research and practice.

methodsThirteen co-researchers (six patients and seven household carers, mean age 47 years) receiving community-based palliative care, attended nine half-day group sessions over a 4-month period. Co-researchers produced, selected and analysed photographs. On completion of data collection, they conducted an advocacy event, including a photographic exhibition, to which media representatives and community leaders were invited.

resultsProcedures to ensure safety of co-researchers and to obtain consent of individuals identified in the photographs were developed during the planning phase. Co-researchers engaged with the Photovoice process with enthusiasm, although frailty and physical disability (poor sight) limited participation for some older adults. Inclusion of palliative care staff within the research team helped to facilitate open dialogue and clinical review where appropriate.

conclusionsIn this Photovoice study, patients and family members receiving palliative care engaged in an exploration of household well-being using photography, participatory analysis and an advocacy event. With appropriate planning, Photovoice can be adapted to a range of settings to enhance patient participation.

Indexed as

PhotographyAdultCaregiversCommunity-Based Participatory ResearchHumansInformed ConsentMalawiMiddle AgedPalliative CarePatientsResearch Subjectscancerpalliativeparticipatory methodspatient involvementqualitative research

Identifiers

PMID29420196
PMCPMC5969331
OpenAlexW2787366647

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.