Cited by 80Nursing care and researchPalliative Care and End-of-Life IssuesPalliative and Oncologic Care

The DOI matches its Crossref record; 68 of the 68 references it cites were found in a registry or an index.

Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers

Open access

Abstract

Objective: The burden experienced by informal caregivers (ICs) of patients with advanced cancer is well documented. ICs are at risk for anxiety and depression, as well as existential concerns that arise when a loved one is facing a terminal illness. Few psychosocial interventions focus on existential concerns of ICs. However, a growing body of literature indicates that finding meaning in the experience of being an IC for a person with cancer has the potential to buffer against burden. The purpose of this study was to collect preliminary descriptive data regarding caregiver burden, meaning, and psychosocial service use to inform the adaptation of a meaning-centered intervention for ICs. Method: Twenty-five caregivers and 32 patients completed brief, anonymous questionnaires that asked about their role as a caregiver or their perception of their loved one as a caregiver, caregiver burden, and psychosocial service use. Results: Caregivers and patients identified anxiety and depression as top correlates of burden experienced by caregivers, whereas guilt, issues with role/sense of identity, and self-care were additional areas of concern. The majority of caregivers were not receiving psychosocial services, although they almost unanimously reported desiring services. A greater proportion of patients than caregivers believed that an intervention designed to enhance meaning would ameliorate burden, but, nevertheless, close to three quarters of caregivers reported interest in participating in such an intervention. Significance of results: These study findings provide further support for, at a minimum, engaging ICs of persons with advanced cancer in interventions that address existential issues, mental health, self-care, and service use. Such interventions are likely to improve the quality of life of both patients with cancer and their ICs.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1017/s1478951513000084

Cites

68 of 68 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 5

  1. Frankl, 1973, Theories of Psychopathology and Personality
  2. Lichtenthal W.G. , Poppito S. , Olden M. , (2008). Facets of meaning: Differential effects of meaning-centered psychotherapy among advanced cancer patients. Poster presented at the Association for Death Education and Counseling 30th Annual Conference, Montreal, QC, Canada.
  3. 2008, Retooling for an Aging America: Building the Health Care Workforce
  4. Frankl, 1978, The Unheard Cry for Meaning
  5. Frankl, 1967, Psychotherapy and Existentialism

Cited by

Sorted by citations

Metadata

Authors
Applebaum, A. J., Farran, C. J., Marziliano, A. M., Pasternak, A. R., & Breitbart, W.
Affiliations
  • Memorial Sloan Kettering Cancer Center (US)
  • Rush University (US)
  • Dartmouth College (US)
Corresponding author
Applebaum, Allison J.
Venue
Palliative and Supportive Care
Published
2013-08-07
Volume
12
Issue
2
Pages
139-148
ISSN
  • 1478-9515 (ISSN-L)
  • 1478-9523
OpenAlex
W2069348192
Cited by
80
References
68
Citations by year
2026: 6 · 2025: 3 · 2024: 19 · 2023: 8 · 2022: 4 · 2021: 11 · 2020: 4 · 2019: 8 · 2018: 3 · 2017: 4 · 2016: 3 · 2015: 4 · 2014: 2 · 2013: 1
FWCI
6.33
Type
journal article
Language
en
Open access
Locations
  • Palliative & Supportive Care (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Cancer Institute (P30CA008748)
Topics
  • Health Sciences › Nursing › Research and Theory › Nursing care and research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
Keywords
caregiver burden, meaning in life, existential concerns, anxiety, depression, guilt, caregiver identity, self-care, advanced cancer, terminal illness, caregiver mental health
MeSH terms
Activities of Daily Living, Anxiety, Cancer Care Facilities, Counseling, Depression, Family Relations, Humans, Neoplasms, Outpatients, Surveys and Questionnaires, Social Support, Stress, Psychological, Caregivers

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review