Enhancing the quality of life of dementia caregivers from different ethnic or racial groups - A randomized, controlled trial

被引:526
作者
Belle, Steven H.
Burgio, Louis
Burns, Robert
Coon, David
Czaja, Sara J.
Gallagher-Thompson, Dolores
Gitlin, Laura N.
Klinger, Julie
Koepke, Kathy Mann
Lee, Chin Chin
Martindale-Adam, Jennifer
Nichols, Linda
Schulz, Richard
Stahl, Sidney
Stevens, Alan
Winter, Laraine
Zhang, Song
机构
[1] Univ Pittsburgh, Pittsburgh, PA 15260 USA
[2] Univ Alabama, Tuscaloosa, AL USA
[3] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
[4] Geriatr Grp Memphis, Memphis, TN USA
[5] Arizona State Univ, Tempe, AZ USA
[6] Univ Miami, Miami, FL 33152 USA
[7] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
[8] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
[9] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[10] NINR, Bethesda, MD 20892 USA
[11] NIH, Bethesda, MD 20892 USA
[12] Scott & White Mem Hosp & Clin, Temple, TX 76508 USA
关键词
D O I
10.7326/0003-4819-145-10-200611210-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Caring for a family member with dementia is extremely stressful, contributes to psychiatric and physical illness among caregivers, and increases the risk for caregiver death. Finding better ways to support family caregivers is a major public health challenge. Objective: To test the effects of a structured multicomponent intervention on quality of life and clinical depression in caregivers and on rates of institutional placement of care recipients in 3 diverse racial or ethnic groups. Design: Randomized, controlled trial. Setting: In-home caregivers in 5 U.S. cities. Participants: 212 Hispanic or Latino, 219 white or Caucasian, and 211 black or African-American caregivers and their care recipients with Alzheimer disease or related disorders. Intervention: Caregivers within each racial or ethnic group were randomly assigned to an intervention or to a control group. The intervention addressed caregiver depression, burden, self-care, and social support and care recipient problem behaviors through 12 in-home and telephone sessions over 6 months. Caregivers in the control group received 2 brief "check-in" telephone calls during the 6-month intervention. Measurements: The primary outcome was a quality-of-life indicator comprising measures of 6-month caregiver depression, burden, self-care, and social support and care recipient problem behaviors. Secondary outcomes were caregiver clinical depression and institutional placement of the care recipient at 6 months. Results: Hispanic or Latino and white or Caucasian caregivers in the intervention group experienced significantly greater improvement in quality of life than those in the control group (P < 0.001 and P = 0.037, respectively). Black or African-American spouse caregivers also improved significantly more (P = 0.003). Prevalence of clinical depression was lower among caregivers in the intervention group (12.6% vs. 22.7%; P = 0.001). There were no statistically significant differences in institutionalization at 6 months. Limitations: The study used only a single 6-month follow-up assessment, combined heterogeneous cultures and ethnicities into a single group, and excluded some ethnic groups. Conclusions: A structured multicomponent intervention adapted to individual risk profiles can increase the quality of life of ethnically diverse dementia caregivers.
引用
收藏
页码:727 / 738
页数:12
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