Evidence map›Paper›PMID 39627126›Full record

ArticleBMJ open2024

Being kind to ourselves: group compassion-focused therapy (CFT) versus treatment as usual (TAU) to improve depression and anxiety in dementia - a protocol for a mixed-methods feasibility randomised controlled trial within the NHS.

Aimee Spector, Melissa Melville, Catriona Craig, Catherine Henderson, Syd Hiskey, Martin Knapp, Yvette Kusel, Keith Oliver, Louise Robinson, Lindsay Royan and 3 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Aimee SpectorDepartment of Clinical Health Psychology, University College London, London, UK.ORCID http://orcid.org/0000-0003-4448-8143
Melissa MelvilleDepartment of Clinical Health Psychology, University College London, London, UK melissa.melville@nelft.nhs.uk.ORCID http://orcid.org/0009-0005-7110-5197
Catriona CraigBuckinghamshire's Older People's Psychological Services, Saffron House, Easton Street, High Wycombe, Oxford Health NHS Foundation Trust, Buckinghamshire, UK.
Catherine HendersonCare Policy and Evaluation Centre, The London School of Economics and Political Science, London, UK.
Syd HiskeyPrivate Practice, The Oaks Hospital, Colchester, UK.
Martin KnappCare Policy and Evaluation Centre, The London School of Economics and Political Science, London, UK.
Yvette KuselKent and Medway NHS and Social Care Partnership Trust, Thanet Older Adult Psychology, The Beacon, Manston Road, Ramsgate, UK.
Keith OliverAlzheimer's Society Ambassador, London, UK.
Louise RobinsonNewcastle University Population Health Sciences Institute, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0003-0209-2503
Lindsay RoyanClinical Health Psychology Services, North East London NHS Foundation Trust, London, UK.
Joshua StottAdapt Lab, Research Department of Clinical, Educational and Health Psychology, University College London, London, UK.
Lisa WilliamsMersey Care NHS Foundation Trust, Liverpool, UK.
Rachel EvansSchool of Health Sciences, Bangor University, Bangor, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDepression and anxiety are common in dementia, with a devastating impact. However, there remains a lack of evidence-based psychological therapies for this clinical group. Compassion-focused therapy (CFT), a talking therapy which addresses feelings of shame and stigma, has shown benefits in other clinical populations. This study is a mixed-methods feasibility randomised controlled trial (RCT) of group CFT for people with dementia and symptoms of anxiety and/or depression, to determine if a future definitive RCT is feasible. METHODS AND ANALYSIS: 50 people with mild-to-moderate dementia and symptoms of anxiety and/or depression will be randomised to either the intervention arm (12 sessions of group CFT plus treatment as usual (TAU)) or the control arm (TAU). Primary outcome measures include the feasibility of conducting an RCT in terms of recruitment, acceptability, suitability of secondary outcome measures and fidelity. Blind assessments will be conducted at baseline, approximately 16 weeks and 6 months follow-up, to collect data on depression, anxiety, quality of life, quality of the carer-patient relationship, cognition, self-compassion and carer burden. Qualitative interviews will be used to gather participant, carer/supporter and clinician perspectives on the value, acceptability and feasibility of the intervention. ETHICS AND DISSEMINATION: This study has been approved by the London Riverside REC (Ref: 23/LO/0535) and the Health Research Authority (HRA) ethical approval process through the Integrated Research Application System (IRAS ID: 327086). We plan to publish the results in open-access peer-reviewed journals, present data at conferences and provide feedback to the study participants, sponsors and funders. TRIAL REGISTRATION NUMBER: ISRCTN20868432.

Indexed as

AnxietyDementiaDepressionEmpathyFeasibility StudiesPsychotherapy, GroupQuality of LifeCaregiversHumansRandomized Controlled Trials as TopicState MedicineUnited KingdomAnxiety disordersDementiaDepression & mood disordersFeasibility StudiesPsychosocial Intervention

Identifiers

PMID39627126
PMCPMC11628998

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Registered trials

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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.