Literature DB >> 14572844

Family caregiver perspective-taking and accuracy in estimating cancer patient symptom experiences.

Michelle M Lobchuk1, Jacquie D Vorauer.   

Abstract

As family caregivers assume more prominent roles in the provision of home care to persons with serious illness, investigators must test the effectiveness of novel interventions to facilitate family caring for cancer patients. This article is based on results derived from a larger study carried out in Canada that was designed to compare 98 advanced cancer patient and family caregiver perceptions of 32 patient symptom experiences as captured by the Memorial Symptom Assessment Scale. We examined two main questions: (1) whether "natural" family caregivers' perceptions of patient lack of energy and worrying are more closely related to a self- or patient-oriented viewpoint and (2) whether induced "imagine-patient" perspective-taking can assist caregivers to achieve better perceptual accuracy. The caregiver's natural responses to neutral instructions that neither encouraged nor discouraged perspective-taking served as the baseline comparison with three other instructional sets, in which caregivers were prompted to: (1) provide a self-report on their own symptom experiences, (2) imagine how they would feel in the patient's situation (imagine-self), or (3) imagine how the patient would respond to his or her symptom situation (imagine-patient). Findings suggested that the family caregivers' natural judgments correspond most closely to what they do under an imagine-patient set than to what they do under any other set. Findings with respect to accuracy indicated that instructions to imagine the patient's perspective helped to prompt adjustments down from a self-oriented viewpoint, although definitive conclusions were precluded by difficulties with order effects.

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Year:  2003        PMID: 14572844     DOI: 10.1016/s0277-9536(03)00132-1

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  8 in total

1.  Measuring Spiritual Well-Being in Brazilian Adolescents with Chronic Illness Using the FACIT-Sp-12: Age Adaptation of the Self-Report Version, Development of the Parental-Report Version, and Validation.

Authors:  Willyane Andrade de Alvarenga; Lucila Castanheira Nascimento; Claudia Benedita Dos Santos; Ana Carolina Andrade Biaggi Leite; Holger Mühlan; Silke Schmidt; Monika Bullinger; Emília Campos de Carvalho; Jason Bredle; Benjamin Arnold; Robson de Castro Coelho; Margarida Vieira
Journal:  J Relig Health       Date:  2019-12

2.  Challenge of assessing symptoms in seriously ill intensive care unit patients: can proxy reporters help?

Authors:  Kathleen A Puntillo; John Neuhaus; Shoshana Arai; Steven M Paul; Michael A Gropper; Neal H Cohen; Christine Miaskowski
Journal:  Crit Care Med       Date:  2012-10       Impact factor: 7.598

3.  Agreement Between Responses From Community-Dwelling Persons With Stroke and Their Proxies on the NIH Neurological Quality of Life (Neuro-QoL) Short Forms.

Authors:  Allan J Kozlowski; Ritika Singh; David Victorson; Ana Miskovic; Jin-Shei Lai; Richard L Harvey; David Cella; Allen W Heinemann
Journal:  Arch Phys Med Rehabil       Date:  2015-07-21       Impact factor: 3.966

4.  Symptom profiles in children with advanced cancer: Patient, family caregiver, and oncologist ratings.

Authors:  Donna S Zhukovsky; Cathy L Rozmus; Rhonda S Robert; Eduardo Bruera; Robert J Wells; Gary B Chisholm; Julio A Allo; Marlene Z Cohen
Journal:  Cancer       Date:  2015-07-28       Impact factor: 6.860

5.  Symptom cluster experience profiles in adult survivors of childhood cancers.

Authors:  Lorna Finnegan; Richard T Campbell; Carol Estwing Ferrans; JoEllen Wilbur; Diana J Wilkie; Joan Shaver
Journal:  J Pain Symptom Manage       Date:  2009-06-16       Impact factor: 3.612

Review 6.  Improving well-being in caregivers of terminally ill patients. Making the case for patient suffering as a focus for intervention research.

Authors:  Randy S Hebert; Robert M Arnold; Richard Schulz
Journal:  J Pain Symptom Manage       Date:  2007-07-05       Impact factor: 3.612

7.  Comparing two types of perspective taking as strategies for detecting distress amongst parents of children with cancer: A randomised trial.

Authors:  Lucie Gouveia; Annie Janvier; France Dupuis; Michel Duval; Serge Sultan
Journal:  PLoS One       Date:  2017-04-06       Impact factor: 3.240

8.  Communication in Oncology Outpatient Clinic Settings: Congruence of Quality of Life Assessment between Patient-Physician and Patient-Caregiver Dyads.

Authors:  Chia-Chun Tang; Chen Hsi; Wu Wei-Wen; I-Ni Tsai; Tsai Jaw-Shiun
Journal:  J Oncol       Date:  2022-08-25       Impact factor: 4.501

  8 in total

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