Department of Ophthalmology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
J Am Geriatr Soc. 2010 Jan;58(1):30-7. doi: 10.1111/j.1532-5415.2009.02631.x.
To examine the relationships between changes from baseline to post-Resources for Enhancing Alzheimer's Caregiver Health (REACH) intervention in caregiver (CG) self-reported health, burden, and bother.
Randomized, multisite clinical trial.
CG and care recipient (CR) homes in five U.S. cities.
Four hundred ninety-five dementia CG and CR dyads (169 Hispanic, 160 white, and 166 African American) receiving intervention and their controls.
CGs were assigned to the REACH intervention or a no-treatment control group. Intervention subjects received individual risk profiles and the REACH intervention through nine in-home and three telephone sessions over 6 months. Control subjects received two brief "check-in" telephone calls during this 6-month period.
The primary outcome was change in CG health status from baseline to after the intervention. Secondary outcomes were CG burden and bother after the intervention.
After the intervention, CGs reported better self-rated health, sleep quality, physical health, and emotional health, which was related to less burden and bother with their caregiving role than for CGs not receiving the intervention. Changes in depression appeared to mediate these relationships. Several racial and ethnic group differences existed in physical and emotional health, as well as in total frustration with caregiving, emotional burden, and CG-rated bother with CR's activities of daily living and instrumental activities of daily living at baseline and at follow-up, although differences between baseline and posttest did not vary according to race.
A structured, multicomponent skills training intervention that targeted CG self-care behaviors as one of five target areas, improved self-reported health status, and decreased burden and bother in racially and ethnically diverse CGs of people with dementia.
考察基线至增强阿尔茨海默病照护者健康资源(REACH)干预后照护者(CG)自我报告的健康、负担和困扰变化之间的关系。
随机、多地点临床试验。
五个美国城市的 CG 和照护对象(CR)家庭。
接受干预的 495 对痴呆症 CG 和 CR (169 名西班牙裔、160 名白人和 166 名非裔美国人)及其对照组。
CG 被分配到 REACH 干预组或无治疗对照组。干预组接受了个人风险概况和 REACH 干预,共 9 次家访和 3 次电话咨询,持续 6 个月。对照组在这 6 个月期间接受了两次简短的“检查”电话。
主要结果是干预后 CG 健康状况的变化。次要结果是干预后的 CG 负担和困扰。
干预后,CG 报告自我评估的健康状况、睡眠质量、身体健康和情绪健康状况有所改善,与未接受干预的 CG 相比,他们的照护角色负担和困扰较少。抑郁的变化似乎介导了这些关系。在基线和随访时,存在一些种族和民族群体在身体和情绪健康以及对照护的总体挫折感、情绪负担以及 CG 对 CR 日常生活活动和工具性日常生活活动的困扰方面的差异,尽管基线和后测之间的差异与种族无关。
一项针对 CG 自我保健行为的结构化、多成分技能培训干预措施,改善了种族和民族多样化的痴呆症 CG 的自我报告健康状况,并降低了负担和困扰。