University of North Carolina, Chapel Hill.
Arthritis Care Res (Hoboken). 2013 Feb;65(2):203-11. doi: 10.1002/acr.21781.
To determine if there are differences or similarities in arthritis intervention preferences and barriers to participation between African Americans and whites with osteoarthritis (OA).
Using a needs assessment survey, intervention preferences and barriers to participation in arthritis interventions among African American (n = 60) and white (n = 55) adults with self-reported doctor-diagnosed OA were examined. T-tests, chi-square tests, and multiple regression analyses adjusting for covariates were examined to determine race effects.
While there were many similarities, African Americans were more likely to report cost (P < 0.01), lack of trust (P = 0.04), fear of being the only person of their race (P < 0.001), lack of recommendation from their doctor (P = 0.04), and lack of recommendation of a family member or friend (P = 0.02) as barriers to participating in a community-based self-management arthritis intervention. After adjusting for covariates, African Americans preferred interventions that provide information on arthritis-related internet sources (P = 0.04), solving arthritis-related problems (P = 0.04), and talking to family and friends about their condition (P = 0.02) in comparison to whites. African Americans also preferred an intervention with child care services provided (P < 0.01), with instructors and participants of the same race (P < 0.01 and P < 0.001, respectively) or sex (P < 0.001 and P = 0.03, respectively), that allows a friend (P = 0.001) or family member (P = 0.02) to attend, that is offered at a local church (P = 0.01) or clinic (P < 0.01), or that is mailed (P < 0.01).
Findings suggest that similar interventions are preferred across racial groups, but some practical adaptations could be made to existing arthritis interventions to minimize barriers, increase cultural sensitivity, and offer programs that would be appealing to African Americans and whites with arthritis.
确定非裔美国人和白人骨关节炎(OA)患者在关节炎干预偏好和参与障碍方面是否存在差异或相似之处。
使用需求评估调查,检查了 60 名自我报告经医生诊断为 OA 的非裔美国人和 55 名白人成年人对关节炎干预措施的干预偏好和参与障碍。使用 t 检验、卡方检验和多元回归分析调整协变量,以确定种族效应。
虽然有许多相似之处,但非裔美国人更有可能报告费用(P < 0.01)、缺乏信任(P = 0.04)、担心自己是唯一的种族(P < 0.001)、缺乏医生的推荐(P = 0.04),以及缺乏家庭成员或朋友的推荐(P = 0.02)作为参加社区自我管理关节炎干预的障碍。在调整协变量后,与白人相比,非裔美国人更喜欢提供关节炎相关互联网资源信息(P = 0.04)、解决关节炎相关问题(P = 0.04)和与家人和朋友谈论病情(P = 0.02)的干预措施。非裔美国人也更喜欢提供儿童保育服务的干预措施(P < 0.01)、具有相同种族(P < 0.01 和 P < 0.001)或性别的教练和参与者(P < 0.001 和 P = 0.03)、允许朋友(P = 0.001)或家庭成员(P = 0.02)参加、在当地教堂(P = 0.01)或诊所(P < 0.01)提供或邮寄(P < 0.01)的干预措施。
研究结果表明,不同种族群体都倾向于相似的干预措施,但可以对现有的关节炎干预措施进行一些实际调整,以减少障碍、提高文化敏感性,并提供对关节炎患者有吸引力的计划。