Enhancing quality of life and mastery of informal caregivers of high-grade glioma patients: a randomized controlled trial

被引:81
作者
Boele, Florien W. [1 ]
Hoeben, Wopke [1 ]
Hilverda, Karen [1 ]
Lenting, Jeroen [1 ]
Calis, Anne-Lucia [1 ]
Sizoo, Eefje M. [2 ]
Collette, Emma H. [1 ]
Heimans, Jan J. [2 ]
Taphoorn, Martin J. B. [2 ,3 ]
Reijneveld, Jaap C. [2 ,4 ]
Klein, Martin [1 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Med Psychol, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Neurol, NL-1007 MB Amsterdam, Netherlands
[3] Med Ctr Haaglanden, Dept Neurol, NL-2501 CK The Hague, Netherlands
[4] Acad Med Ctr, Dept Neurol, NL-1100 DD Amsterdam, Netherlands
关键词
Quality of life; Mastery; Informal caregiver; Brain tumor; FAMILY CAREGIVERS; PALLIATIVE CARE; CANCER-PATIENTS; BRAIN-TUMOR; DEPRESSION; END; INTERVENTIONS; VALIDATION; SYMPTOMS; DISTRESS;
D O I
10.1007/s11060-012-1012-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High-grade gliomas (HGG) are serious primary brain tumors that may prevent the patient from functioning normally in social, emotional and cognitive respect. Often the partner's role will convert to that of informal caregiver. Consequently, they may experience significant stress and reductions in caregiver mastery, negatively affecting their health-related quality of life (HRQOL). We aimed at (1) determining factors that impact HRQOL and mastery of caregivers of HGG patients, and (2) investigate if a structured intervention consisting of psychoeducation and cognitive behavioral therapy leads to improvements in the mental component of HRQOL and mastery of caregivers. Fifty-six patient-caregiver dyads were randomly assigned to the intervention group or the care as usual group. The intervention program consisted of six one-hour sessions with a psychologist. Participants completed questionnaires concerning their perceptions of the patients' HRQOL (SF-36), neurological functioning (BN20), and cognitive functioning (MOS), and concerning their own HRQOL (SF-36) and feelings of caregiver mastery (CMS) both at baseline (i.e. before randomization) and every 2 months thereafter until 8 months later, five times in total. Patients' HRQOL and neurological functioning were found to be related to HRQOL and feelings of mastery of the informal caregiver at baseline. The intervention helped caregivers in maintaining a stable level of HRQOL and improved feelings of mastery over an 8 month period. Our findings suggest that informal caregivers can benefit from a psychological intervention as it is a helpful tool in maintaining a stable level of mental functioning and caregiver mastery.
引用
收藏
页码:303 / 311
页数:9
相关论文
共 42 条
[1]  
[Anonymous], 1992, Measuring functioning and well-being: The medical outcomes study EApproach
[2]   The mental health of informal caregivers in Ontario: An epidemiological survey [J].
Cochrane, JJ ;
Goering, PN ;
Rogers, JM .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1997, 87 (12) :2002-2007
[3]   Systematic review of supportive care needs in patients with primary malignant brain tumors [J].
Ford, Elizabeth ;
Catt, Susan ;
Chalmers, Anthony ;
Fallowfield, Lesley .
NEURO-ONCOLOGY, 2012, 14 (04) :392-404
[4]  
Given B, 2005, ONCOL NURS FORUM, V31, P1105, DOI [10.1188/04.ONF.1105-1117, DOI 10.1188/04.ONF.1105-1117]
[5]  
Given Barbara A, 2012, J Support Oncol, V10, P57, DOI 10.1016/j.suponc.2011.10.003
[6]  
Haley W E, 2001, Hosp J, V15, P1, DOI 10.1300/J011v15n04_01
[7]   How can informal caregivers in cancer and palliative care be supported? An updated systematic literature review of interventions and their effectiveness [J].
Harding, Richard ;
List, Sally ;
Epiphaniou, Eleni ;
Jones, Hannah .
PALLIATIVE MEDICINE, 2012, 26 (01) :7-22
[8]   Caregiver assessment of patients with advanced cancer: concordance with patients, effect of burden and positivity [J].
Higginson, Irene J. ;
Gao, Wei .
HEALTH AND QUALITY OF LIFE OUTCOMES, 2008, 6 (1)
[9]   A critical review of supportive interventions for family caregivers of patients with palliative-stage cancer [J].
Hudson, P .
JOURNAL OF PSYCHOSOCIAL ONCOLOGY, 2004, 22 (04) :77-92
[10]   A psycho-educational intervention for family caregivers of patients receiving palliative care: A Randomized controlled trial [J].
Hudson, PL ;
Aranda, S ;
Hayman-White, K .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2005, 30 (04) :329-341