Literature DB >> 24245838

CHESS improves cancer caregivers' burden and mood: results of an eHealth RCT.

Lori L DuBenske1, David H Gustafson2, Kang Namkoong3, Robert P Hawkins4, Amy K Atwood2, Roger L Brown5, Ming-Yuan Chih2, Fiona McTavish2, Cindy L Carmack6, Mary K Buss7, Ramaswamy Govindan8, James F Cleary9.   

Abstract

OBJECTIVE: Informal caregivers (family and friends) of people with cancer are often unprepared for their caregiving role, leading to increased burden or distress. Comprehensive Health Enhancement Support System (CHESS) is a Web-based lung cancer information, communication, and coaching system for caregivers. This randomized trial reports the impact on caregiver burden, disruptiveness, and mood of providing caregivers access to CHESS versus the Internet with a list of recommended lung cancer websites.
METHODS: A total of 285 informal caregivers of patients with advanced nonsmall cell lung cancer were randomly assigned to a comparison group that received Internet or a treatment group that received Internet and CHESS. Caregivers were provided a computer and Internet service if needed. Written surveys were completed at pretest and during the intervention period bimonthly for up to 24 months. Analyses of covariance (ANCOVAs) compared the intervention's effect on caregivers' disruptiveness and burden (CQOLI-C), and negative mood (combined Anxiety, Depression, and Anger scales of the POMS) at 6 months, controlling for blocking variables (site, caregiver's race, and relationship to patient) and the given outcome at pretest.
RESULTS: Caregivers randomized to CHESS reported lower burden, t(84) = 2.36, p = .021, d = .39, and negative mood, t(86) = 2.82, p = .006, d = .44, than those in the Internet group. The effect on disruptiveness was not significant.
CONCLUSIONS: Although caring for someone with a terminal illness will always exact a toll on caregivers, eHealth interventions like CHESS may improve caregivers' understanding and coping skills and, as a result, ease their burden and mood.

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Mesh:

Year:  2013        PMID: 24245838      PMCID: PMC4121384          DOI: 10.1037/a0034216

Source DB:  PubMed          Journal:  Health Psychol        ISSN: 0278-6133            Impact factor:   4.267


  57 in total

Review 1.  Positive affect and the other side of coping.

Authors:  S Folkman; J T Moskowitz
Journal:  Am Psychol       Date:  2000-06

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Journal:  Palliat Med       Date:  2011-07-07       Impact factor: 4.762

Review 3.  Family support in advanced cancer.

Authors:  B A Given; C W Given; S Kozachik
Journal:  CA Cancer J Clin       Date:  2001 Jul-Aug       Impact factor: 508.702

Review 4.  Prevalence of pain in patients with cancer: a systematic review of the past 40 years.

Authors:  M H J van den Beuken-van Everdingen; J M de Rijke; A G Kessels; H C Schouten; M van Kleef; J Patijn
Journal:  Ann Oncol       Date:  2007-03-12       Impact factor: 32.976

5.  The relationship between available support, unmet needs and caregiver burden in patients with advanced cancer and their carers.

Authors:  Louise Sharpe; Phyllis Butow; Claire Smith; David McConnell; Stephen Clarke
Journal:  Psychooncology       Date:  2005-02       Impact factor: 3.894

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Authors:  Hoda Badr; Paul Krebs
Journal:  Psychooncology       Date:  2012-10-09       Impact factor: 3.894

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
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8.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

Authors:  Eva Grunfeld; Doug Coyle; Timothy Whelan; Jennifer Clinch; Leonard Reyno; Craig C Earle; Andrew Willan; Raymond Viola; Marjorie Coristine; Teresa Janz; Robert Glossop
Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262

9.  Doctor-patient relationship as motivation and outcome: examining uses of an Interactive Cancer Communication System.

Authors:  Bret R Shaw; Jeong Yeob Han; Robert P Hawkins; James Stewart; Fiona McTavish; David H Gustafson
Journal:  Int J Med Inform       Date:  2006-02-03       Impact factor: 4.046

Review 10.  Needs assessment for cancer patients and their families.

Authors:  Kuang-Yi Wen; David H Gustafson
Journal:  Health Qual Life Outcomes       Date:  2004-02-26       Impact factor: 3.186

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  49 in total

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Review 3.  Health Social Media and Patient-Centered Care: Buzz or Evidence? Findings from the Section "Education and Consumer Health Informatics" of the 2015 Edition of the IMIA Yearbook.

Authors:  P Staccini; L Fernandez-Luque
Journal:  Yearb Med Inform       Date:  2015-08-13

4.  Closer: A videoconference intervention for distance caregivers of cancer patients.

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Journal:  Res Nurs Health       Date:  2019-05-22       Impact factor: 2.228

5.  Characterizing the Nature of Scan Results Discussions: Insights Into Why Patients Misunderstand Their Prognosis.

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Journal:  J Oncol Pract       Date:  2017-01-17       Impact factor: 3.840

Review 6.  Psychosocial interventions for patients and caregivers in the age of new communication technologies: opportunities and challenges in cancer care.

Authors:  Hoda Badr; Cindy L Carmack; Michael A Diefenbach
Journal:  J Health Commun       Date:  2015-01-28

7.  Exploring the cancer caregiver's journey through web-based Meaning-Centered Psychotherapy.

Authors:  A J Applebaum; K L Buda; E Schofield; M Farberov; N D Teitelbaum; K Evans; R Cowens-Alvarado; R S Cannady
Journal:  Psychooncology       Date:  2017-12-19       Impact factor: 3.894

8.  Who cares? The impact on caregivers of suspected mining-related lung cancer.

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9.  Priorities to improve cancer caregiving: report of a caregiver stakeholder workshop.

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Review 10.  Caring for caregivers and patients: Research and clinical priorities for informal cancer caregiving.

Authors:  Erin E Kent; Julia H Rowland; Laurel Northouse; Kristin Litzelman; Wen-Ying Sylvia Chou; Nonniekaye Shelburne; Catherine Timura; Ann O'Mara; Karen Huss
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