Evidence map›Paper›PMID 32065801›Full record

ArticleJournal of Huntington's disease2020

The Ripple Effect: A Qualitative Overview of Challenges When Growing Up in Families Affected by Huntington's Disease.

Siri Kjoelaas, Kristine Hansen Tillerås, Kristin Billaud Feragen

Abstract read
In one paragraph

Article in Journal of Huntington's disease, 2020. 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
–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

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

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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

3 authors.

Siri KjoelaasCentre for Rare Disorders, Oslo University Hospital HF, Rikshospitalet, Nydalen, Oslo, Norway.
Kristine Hansen TilleråsCentre for Rare Disorders, Oslo University Hospital HF, Rikshospitalet, Nydalen, Oslo, Norway.
Kristin Billaud FeragenCentre for Rare Disorders, Oslo University Hospital HF, Rikshospitalet, Nydalen, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe average age for the onset of Huntington's disease (HD) is an age when many people have children and caretaking responsibilities; HD is therefore likely to impact the whole family, including children and adolescents. Despite an increased understanding of the challenges for young people of growing up in a family affected by HD, a continuing lack of available knowledge has led to inadequate youth-focused support in many countries.

objectiveThis study explored the risks of growing up in a family affected by HD, and provided a participant-generated overview of the main challenges the participants experienced, in order to enhance awareness and promote more youth-focused support.

methodsAs part of a larger national study, this qualitative paper included 36 semi-structured interviews with young people and adults who had previous or current experiences of growing up in families affected by HD. The interviews were analysed using thematic analysis.

resultsThe participants described challenges relating to four main domains of everyday life: family functioning, emotions and reactions, social functioning, and public and care services.

conclusionThis study contributes to an increased understanding of risk factors posed on young people by growing up with a parent with HD. The study highlighted challenges in several areas of life presenting a risk to the overall health and functioning of young people. We propose that this knowledge should be applied within a bioecological framework, to increase understanding and promote awareness of the possible risks posed, for young people, by HD.

Indexed as

Health Knowledge, Attitudes, PracticePsychosocial FunctioningSocial WorkAdolescentAdultAdverse Childhood ExperiencesChildChild of Impaired ParentsCommunity ParticipationFamilyFemaleHumansHuntington DiseaseMaleMiddle AgedNorwayAwarenesschallengesHuntington’s diseaseknowledgequalitative researchsupportyoung people

Identifiers

PMID32065801
PMCPMC7369039

What OpenQuestion holds

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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.