Evidence map›Paper›PMID 32565450›Full record

ArticleBMJ open2020

One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial.

Afia Ali, Emma Mckenzie, Angela Hassiotis, Stefan Priebe, Brynmor Lloyd-Evans, Rumana Omar, Rebecca Jones, Monica Panca, Vincent Fernandez, Sally Finning and 4 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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

14 authors.

Afia AliDivision of Psychiatry, University College London, London, UK afia.ali@ucl.ac.uk.ORCID 0000-0002-0104-9370
Emma MckenzieResearch and Development, North East London NHS Foundation Trust Goodmayes Hospital, Ilford, Essex, UK.
Angela HassiotisDivision of Psychiatry, University College London, London, UK.
Stefan PriebeUnit of Social and Community Psychiatry, Barts and the London School of Medicine and Dentistry, University of London, London, UK.
Brynmor Lloyd-EvansDivision of Psychiatry, University College London, London, UK.
Rumana OmarDepartment of Statistical Science, University College London, London, UK.
Rebecca JonesDivision of Psychiatry, University College London, London, UK.
Monica PancaPrimary Care and Population Health, University College London, London, UK.
Vincent FernandezHackney Volunteer and Befriending Scheme, Outward, London, UK.
Sally FinningHackney Volunteer and Befriending Scheme, Outward, London, UK.
Shirley MooreThe Befriending Scheme, Sudbury, Suffolk, UK.
Danielle O'ConnorThe Befriending Scheme, Sudbury, Suffolk, UK.
Christine RoeThe Befriending Scheme, Sudbury, Suffolk, UK.
Michael KingDivision of Psychiatry, University College London, London, UK.

Funding

Department of Health 16/122/57
6 · The paper itself

Abstract

introductionPeople with intellectual disability (ID) are more likely to experience loneliness and have smaller social networks, which increases vulnerability to depression. Befriending may reduce depressive symptoms in other populations, but randomised controlled trials (RCTs) have not been carried out in this population. This pilot study aims to assess the acceptability and feasibility of carrying out a full RCT of one-to-one befriending by volunteers for people with ID, compared with an active control group. METHODS AND ANALYSIS: The trial aims to recruit 40 participants with ID. Participants in the intervention arm will receive weekly visits from a volunteer over 6 months. Community befriending schemes will recruit, train, supervise volunteers and match them to individuals with ID. Both groups will receive a booklet about local activities and have access to usual care. Health and social outcomes will be measured at the end of the intervention and 6 months' follow-up. The following outcomes will be assessed: (1) recruitment and retention of individuals with ID and volunteers in the trial, (2) adverse events related to the intervention, (3) the acceptability of the intervention, (4) whether the intervention is delivered as intended, (5) changes in health and social outcomes and (6) the feasibility of carrying out a cost-effectiveness analysis in a full trial. Qualitative data from participants, volunteers, staff and carers will identify barriers and facilitators of a future full trial. ETHICS AND DISSEMINATION: The study has been approved by the London City and East Research Ethics Committee (reference 18/LO/2188). The findings will be presented at conferences and published in a peer-reviewed journal and in the National Institute of Health Research journals library. A public engagement seminar will be held at the end of the study aimed at key stakeholders. TRIAL REGISTRATION NUMBER: ISRCTN63779614.

Indexed as

Intellectual DisabilityRandomized Controlled Trials as TopicSocial SupportDepressionHumansLonelinessPersons with DisabilitiesPilot ProjectsVolunteersdelirium & cognitive disordersdepression & mood disordersqualitative research

Identifiers

PMID32565450
PMCPMC7311030

What OpenQuestion holds

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LicenceCC BY
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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.