Thomsen C A, Ter Maat J
Cancer Information Service Branch, Office of Cancer Communications, National Cancer Institute, Bethesda, Maryland 20892-2580, USA.
J Health Commun. 1998;3 Suppl:1-13. doi: 10.1080/108107398127210.
The Cancer Information Service (CIS) was established in 1975 by the National Cancer Institute (NCI) to meet the information needs of cancer patients, their families, health professionals, and the public. As the nation's foremost source for cancer information, the CIS applies a unique health communications model to bring the latest research findings on cancer prevention, detection, treatment, and supportive care to the nation. It does this through two main program components: a toll-free telephone service (1-800-4-CANCER) and an outreach program that focuses on providing technical assistance, specifically to partners reaching minority and underserved audiences. During its 22-year history, more than 7.5 million callers have reached the CIS telephone service. In addition, 100,000 requests are received each year from 4,500 organizations nationwide seeking cancer-related outreach expertise. This overview describes the CIS model for health communications, describes the program's impact in broad terms, and defines the critical role evaluation plays in each program component. The overview describes two customer satisfaction and impact surveys performed by an independent survey research firm in 1996 to evaluate the CIS model: (a) the telephone service user survey, a random sample of 2,489 persons representing major caller groups who were interviewed 3 to 6 weeks after their initial call to the CIS; and (b) the outreach partner survey, a random sample of 867 partner organizations, the majority of which reach minority and underserved audiences with information and programs, surveyed within a few months after a contact with the CIS outreach program. Impact data for both program areas were favorable: Approximately 8 out of 10 CIS callers reported that the information they received had a positive impact (either in eliciting a positive action [56%] or in reassurance of decisions made [22%]) and two-thirds of CIS partners said the CIS has an important impact on their programs.
癌症信息服务(CIS)于1975年由美国国立癌症研究所(NCI)设立,以满足癌症患者、其家属、医疗专业人员及公众的信息需求。作为美国最重要的癌症信息来源,CIS采用独特的健康传播模式,将癌症预防、检测、治疗及支持性护理方面的最新研究成果带给全国民众。它通过两个主要项目组成部分来实现这一目标:一项免费电话服务(1-800-4-CANCER)和一项外展项目,该外展项目专注于提供技术援助,特别是针对面向少数族裔和服务不足人群的合作伙伴。在其22年的历史中,超过750万来电者拨打了CIS电话服务。此外,每年收到来自全国4500个组织的10万份请求,这些组织寻求与癌症相关的外展专业知识。本概述描述了CIS的健康传播模式,从广义上描述了该项目的影响,并界定了评估在每个项目组成部分中所起的关键作用。该概述描述了一家独立调查研究公司于1996年进行的两项客户满意度和影响调查,以评估CIS模式:(a)电话服务用户调查,对2489人进行随机抽样,这些人代表主要来电群体,在他们首次致电CIS后的3至6周接受访谈;(b)外展合作伙伴调查,对867个合作伙伴组织进行随机抽样,其中大多数通过信息和项目面向少数族裔和服务不足人群,在与CIS外展项目接触后的几个月内接受调查。两个项目领域的影响数据都很可观:约十分之八的CIS来电者表示他们收到的信息产生了积极影响(要么促使采取积极行动[56%],要么使已做出的决定得到安心[22%]),三分之二的CIS合作伙伴表示CIS对他们的项目有重要影响。