Literature DB >> 20880656

Caregivers' participation in the oncology clinic visit mediates the relationship between their information competence and their need fulfillment and clinic visit satisfaction.

Lori L DuBenske1, Ming-Yuan Chih, David H Gustafson, Susan Dinauer, James F Cleary.   

Abstract

OBJECTIVE: Caregivers maintain critical roles in cancer patient care. Understanding cancer-related information effects both caregiver involvement and ability to have needs met. This study examines the mediating role caregiver's clinic visit involvement has on the relationships between caregiver's information competence and their need fulfillment and clinic visit satisfaction.
METHODS: Secondary analysis of 112 advanced lung, breast, and prostate cancer caregivers participating in a large clinical trial. Caregiver information competence was assessed at pretest. Involvement, need fulfillment, and visit satisfaction were assessed immediately following the clinic appointment.
RESULTS: Involvement correlated with information competence (r=.21, p<.05), need fulfillment (r=.48, p<.001), and satisfaction (r=.35, p<.001). The correlation between information competence and need fulfillment (r=.26, p<.01) decreased when controlling for involvement (r=.19, p=.049), demonstrating mediation, and accounted for 24.4% of the variance in need fulfillment. The correlation between information competence and satisfaction (r=.21, p=.04), decreased and was non-significant when controlling for involvement (r=.15, p=.11), demonstrating mediation, and accounted for 13% of variance in visit satisfaction.
CONCLUSION: Caregiver's clinic visit involvement mediates the relationships between their information competence and their need fulfillment and visit satisfaction. PRACTICE IMPLICATIONS: Efforts to improve the caregiving experience, and potentially patient outcomes, should focus on system-wide approaches to facilitating caregivers' involvement and assertiveness in clinical encounters.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20880656      PMCID: PMC2993845          DOI: 10.1016/j.pec.2010.08.022

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  48 in total

Review 1.  Work system design for patient safety: the SEIPS model.

Authors:  P Carayon; A Schoofs Hundt; B-T Karsh; A P Gurses; C J Alvarado; M Smith; P Flatley Brennan
Journal:  Qual Saf Health Care       Date:  2006-12

2.  Levels of depressive symptoms in spouses of people with lung cancer: effects of personality, social support, and caregiving burden.

Authors:  Youngmee Kim; Paul R Duberstein; Silvia Sörensen; Mark R Larson
Journal:  Psychosomatics       Date:  2005 Mar-Apr       Impact factor: 2.386

3.  How women with breast cancer learn using interactive cancer communication systems.

Authors:  Bret R Shaw; Jeong Yeob Han; Timothy Baker; Jeffre Witherly; Robert P Hawkins; Fiona McTavish; David H Gustafson
Journal:  Health Educ Res       Date:  2006-07-07

4.  Physicians' communication with a cancer patient and a relative: a randomized study assessing the efficacy of consolidation workshops.

Authors:  Nicole Delvaux; Isabelle Merckaert; Serge Marchal; Yves Libert; Sandrine Conradt; Jacques Boniver; Anne-Marie Etienne; Ovide Fontaine; Pascal Janne; Jean Klastersky; Christian Mélot; Christine Reynaert; Pierre Scalliet; Jean-Louis Slachmuylder; Darius Razavi
Journal:  Cancer       Date:  2005-06-01       Impact factor: 6.860

5.  Caring for the brain tumor patient: family caregiver burden and unmet needs.

Authors:  Jane R Schubart; Mable B Kinzie; Elana Farace
Journal:  Neuro Oncol       Date:  2007-11-09       Impact factor: 12.300

6.  Caregivers' differing needs across key experiences of the advanced cancer disease trajectory.

Authors:  Lori L DuBenske; Kuang-Yi Wen; David H Gustafson; Charles A Guarnaccia; James F Cleary; Susan K Dinauer; Fiona M McTavish
Journal:  Palliat Support Care       Date:  2008-09

Review 7.  A systematic review of informal caregivers' needs in providing home-based end-of-life care to people with cancer.

Authors:  Penny E Bee; Pamela Barnes; Karen A Luker
Journal:  J Clin Nurs       Date:  2009-04-08       Impact factor: 3.036

8.  Family caregiver engagement in a coping and communication support intervention tailored to advanced cancer patients and families.

Authors:  Karen F Bowman; Julia H Rose; Rosanne M Radziewicz; Elizabeth E O'Toole; Rose A Berila
Journal:  Cancer Nurs       Date:  2009 Jan-Feb       Impact factor: 2.592

9.  Companion participation in cancer consultations.

Authors:  Richard L Street; Howard S Gordon
Journal:  Psychooncology       Date:  2008-03       Impact factor: 3.894

10.  A study of information seeking by cancer patients and their carers.

Authors:  N James; H Daniels; R Rahman; C McConkey; J Derry; A Young
Journal:  Clin Oncol (R Coll Radiol)       Date:  2007-03-30       Impact factor: 4.126

View more
  7 in total

Review 1.  Family Caregivers' Unmet Needs in Long-term Cancer Survivorship.

Authors:  Youngmee Kim; Charles S Carver; Amanda Ting
Journal:  Semin Oncol Nurs       Date:  2019-06-20       Impact factor: 2.315

2.  The Effects of Social Support on Health-Related Quality of Life of Patients with Metastatic Prostate Cancer.

Authors:  Giuseppe Colloca; Pasquale Colloca
Journal:  J Cancer Educ       Date:  2016-06       Impact factor: 2.037

3.  Satisfaction with oncology care among patients with advanced cancer and their caregivers.

Authors:  Breffni Hannon; Nadia Swami; Monika K Krzyzanowska; Natasha Leighl; Gary Rodin; Lisa W Le; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2013-02-23       Impact factor: 4.147

4.  Unmet needs of family cancer caregivers predict quality of life in long-term cancer survivorship.

Authors:  Youngmee Kim; Charles S Carver
Journal:  J Cancer Surviv       Date:  2019-07-24       Impact factor: 4.442

5.  The role of families in decisions regarding cancer treatments.

Authors:  Gabriela S Hobbs; Mary Beth Landrum; Neeraj K Arora; Patricia A Ganz; Michelle van Ryn; Jane C Weeks; Jennifer W Mack; Nancy L Keating
Journal:  Cancer       Date:  2015-02-23       Impact factor: 6.860

6.  Why do patients and caregivers seek answers from the Internet and online lung specialists? A qualitative study.

Authors:  Romane Milia Schook; Cilia Linssen; Franz Mnh Schramel; Jan Festen; Ernst Lammers; Egbert F Smit; Pieter E Postmus; Marjan J Westerman
Journal:  J Med Internet Res       Date:  2014-02-04       Impact factor: 5.428

7.  Efficacy and cost-effectiveness of an outcall program to reduce carer burden and depression among carers of cancer patients [PROTECT]: rationale and design of a randomized controlled trial.

Authors:  Patricia M Livingston; Richard H Osborne; Mari Botti; Cathy Mihalopoulos; Sean McGuigan; Leila Heckel; Kate Gunn; Jacquie Chirgwin; David M Ashley; Melinda Williams
Journal:  BMC Health Serv Res       Date:  2014-01-06       Impact factor: 2.655

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.