Evidence map›Paper›PMID 38652165›Full record

ArticleThe oncologist2024

The cancer caregiving burden trajectory over time: varying experiences of perceived versus objectively measured burden.

Laura A Siminoff, Maureen Wilson-Genderson, Marcin Chwistek, Maria Thomson

Abstract read
In one paragraph

Article in The oncologist, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Quality of life and burden in family caregivers of advanced cancer patients in the Grand Duchy of Luxembourg: results from a single-centre study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  4. Article
  5. Article
  6. Review
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

4 authors.

Laura A SiminoffCollege of Public Health, Social and Behavioral Sciences, Temple University, Philadelphia, PA, United States.ORCID 0000-0002-6775-665X
Maureen Wilson-GendersonCollege of Public Health, Social and Behavioral Sciences, Temple University, Philadelphia, PA, United States.ORCID 0000-0002-6361-358X
Marcin ChwistekFox Chase Cancer Center/Temple University Health, Philadelphia, PA, United States.ORCID 0000-0003-4036-8232
Maria ThomsonDepartment of Health Behavior and Policy, School of Population Health, Virginia Commonwealth University, Richmond, VA, United States.ORCID 0000-0002-5729-8720

Funding

Informal caregiver burden in advanced cancer: Economic and health outcomesR01CA196576 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI SIMINOFF, LAURA A., THOMSON, MARIA D. · 2015 to 2019
$3.8M
NCI NIH HHS R01 CA196576NCI NIH HHS R01CA196576
6 · The paper itself

Abstract

introductionThe objective of this study was to comprehensively understand the burden experienced by caregivers (CGs) providing home-based, end-of-life care to patients with cancer. We examined the relationship between objective and subjective burden including whether and how burden changes over time.

methodsA case series of terminal cancer patient-caregiver dyads (n = 223) were recruited from oncology clinics and followed for 12 months or until patient death. Data were collected every other week and in-person from CGs in their homes using quantitative surveys, diaries, and monthly structured observations.

resultsBivariate correlations revealed a significant association between subjective burden and activities of daily living (ADLs), instrumental activities of daily living (IADL), high-intensity tasks, and time spent on ADLs; these correlations varied over time. Models examining the slope of subjective burden revealed little systematic change; spouse caregiver and patient functional limitations were positively, and Black caregiver was negatively associated with subjective burden. Generally, the slopes for measures of objective burden were significant and positive. Models showed subjective burden was positively associated with most measures of objective burden both within caregiver (concurrent measures were positively associated) and between CGs (those with higher subjective also had higher objective).

conclusionsCancer caregiving is dynamic; CGs must adjust to the progression of the patient's disease. We found an association between subjective and objective burden both within and between CGs. Black CGs were more likely to report lower subjective burden compared to their White counterparts. More detailed investigation of the sociocultural components that affect caregiver experience of burden is needed to better understand how and where to best intervene with targeted supportive care services.

Indexed as

Activities of Daily LivingCaregiversNeoplasmsAdultAgedAged, 80 and overCaregiver BurdenCost of IllnessFemaleHumansMaleMiddle AgedTerminal Carecancer objective caregiver burdencaregiver stressend-of-life carehome and community-based care and serviceslate-stage cancer caresubjective caregiver burden

Identifiers

PMID38652165
PMCPMC11224987

What OpenQuestion holds

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LicenceCC BY-NC
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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.