Evidence map›Paper›PMID 35893316›Full record

ArticleJournal of personalized medicine2022

Using a Clinical Formulation to Understand Psychological Distress in People Affected by Huntington's Disease: A Descriptive, Evidence-Based Model.

Maria Dale, Ashleigh Wood, Nicolò Zarotti, Fiona Eccles, Sarah Gunn, Reza Kiani, Amanda Mobley, Noelle Robertson, Jane Simpson

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% 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, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

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  11. The validation of the Italian version of multiple sclerosis neuropsychological screening questionnaire in Huntington's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
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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

9 authors at 3 institutions in 1 country.

Maria DaleHuntington's Disease Service, Leicestershire Partnership NHS Trust, Mill Lodge, The Rise, Narborough, Leicester LE19 4SL, UK.
Ashleigh WoodHuntington's Disease Service, Leicestershire Partnership NHS Trust, Mill Lodge, The Rise, Narborough, Leicester LE19 4SL, UK.
Nicolò ZarottiDivision of Health Research, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UK.ORCID 0000-0002-8129-6151
Fiona EcclesDivision of Health Research, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UK.ORCID 0000-0003-1484-2703
Sarah GunnHuntington's Disease Service, Leicestershire Partnership NHS Trust, Mill Lodge, The Rise, Narborough, Leicester LE19 4SL, UK.ORCID 0000-0002-8492-060X
Reza KianiHuntington's Disease Service, Leicestershire Partnership NHS Trust, Mill Lodge, The Rise, Narborough, Leicester LE19 4SL, UK.
Amanda MobleyHuntington's Disease Service, Leicestershire Partnership NHS Trust, Mill Lodge, The Rise, Narborough, Leicester LE19 4SL, UK.
Noelle RobertsonDepartment of Neuroscience, Psychology and Behaviour, University of Leicester, University Road, Leicester LE1 7RH, UK.
Jane SimpsonDivision of Health Research, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UK.ORCID 0000-0001-5071-4077
Lancaster University · GBLeicestershire Partnership NHS Trust · GBUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Huntington's disease (HD) is an inherited, life-limiting neurodegenerative condition. People with HD experience changes in cognitive, motor and emotional functioning, and can also, mainly at later stages, exhibit behaviours that professionals and carers might find distressing such as hitting others, throwing objects, swearing or making inappropriate comments. While clinical formulation (an individualised approach used by mental health professionals to describe an individual's difficulties) is a helpful tool to conceptualise patients' wellbeing, a specific formulation framework has not yet been developed for HD. However, evidence has shown that formulation can help guide clinical interventions and increase consistency of approach across multi-disciplinary teams, refine risk management, and improve staff or carers' empathic skills and understanding of complex presentations. As a consequence, this paper proposes a new clinical formulation model for understanding distress among people with HD, based on a biopsychosocial framework. More specifically, this includes key elements centring on an individual's past experience and personal narratives, as well as anticipatory cognitions and emotions about the future. In-depth discussions regarding the components of the model and their importance in HD formulations are included, and a fictional yet representative case example is presented to illustrate their application within the context of personalised care.

Indexed as

biopsychosocialchallenging behaviourformulationHuntington’s diseasepsychological distress

Identifiers

PMID35893316
PMCPMC9332789
OpenAlexW4288077792

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.