Evidence map›Paper›PMID 28699777›Full record

ArticleAging & mental health2018

Caring for an individual with mild cognitive impairment: a qualitative perspective of health-related quality of life from caregivers.

Noelle E Carlozzi, Carey W Sherman, Kaley Angers, Mitchell P Belanger, Amy M Austin, Kelly A Ryan

Abstract read
In one paragraph

Article in Aging & mental health, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  7. Contextualizing Caregiver Burden in Mild Cognitive Impairment: A Dyadic Perspective.International journal of environmental research and public health · 2025
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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

6 authors.

Noelle E Carlozzia Department of Physical Medicine and Rehabilitation , University of Michigan , Ann Arbor , MI , USA.
Carey W Shermanb Institute for Social Research, University of Michigan , Ann Arbor , MI , USA.
Kaley Angersc Department of Psychiatry , University of Michigan , Ann Arbor , MI , USA.
Mitchell P Belangera Department of Physical Medicine and Rehabilitation , University of Michigan , Ann Arbor , MI , USA.
Amy M Austina Department of Physical Medicine and Rehabilitation , University of Michigan , Ann Arbor , MI , USA.
Kelly A Ryanc Department of Psychiatry , University of Michigan , Ann Arbor , MI , USA.

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Michigan Institute for Clinical and Health Research (MCHR)KL2TR000434 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$1.7M
NCATS NIH HHS KL2 TR000434NCATS NIH HHS UL1 TR002240
6 · The paper itself

Abstract

objectivesLittle is known regarding the effect that caring for an individual with Mild Cognitive Impairment (MCI) has on health-related quality of life (HRQOL). We sought to identify the most important aspects of HRQOL related to caring for an individual with MCI.

methodsSix focus groups were conducted with caregivers of individuals with MCI (n = 32). Qualitative frequency analysis was used to analyze the data.

resultsFindings indicated that caregivers most frequently discussed social health, including changes in social roles and an increased need for social support (51.2% of the total discussion). This was followed by mental health concerns (37.9%) centering on anger/frustration, and a need for patience in the caregiving role, as well as caregiver-specific anxiety. Other topics included physical health (10.0%; including the impact that stress and burden have on medical heath), and caregivers' cognitive health (0.9%; including memory problems in relation to caregiver strain, sleep disruption, and cognitive fatigue).

conclusionsFindings illustrate the multiple domains of HRQOL that are affected in individuals providing care for someone with MCI. Moreover, the findings highlight the need for extending support services to MCI caregivers, a group that is typically not offered support services due to the 'less severe' nature of an MCI diagnosis.

Indexed as

Cost of IllnessQuality of LifeSocial SupportAdultAgedAged, 80 and overAngerAnxietyCaregiversCognitive DysfunctionFemaleFocus GroupsFrustrationHealth StatusHumansMalecaregivercognitive disordersfocus groupsMild cognitive impairmentqualitative researchquality of life

Identifiers

PMID28699777
PMCPMC6141353

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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.