Evaluation of Factors Affecting Awareness of and Willingness to Participate in Cancer Clinical Trials

2005 ◽  
Vol 23 (36) ◽  
pp. 9282-9289 ◽  
Author(s):  
Primo N. Lara ◽  
Debora A. Paterniti ◽  
Christine Chiechi ◽  
Corinne Turrell ◽  
Claudia Morain ◽  
...  

Purpose Annually, only 3% of patients participate in cancer clinical trials (CCTs). Barriers to accrual include lack of CCT awareness and uncertain third-party payer coverage. In January 2002, a California law (Senate Bill 37 [SB37]) required all third-party payers to reimburse patient care costs related to CCTs. We evaluated the level of awareness of patients and/or their family members/friends regarding CCTs and SB37. Methods We used both a written survey for patients and/or their family members and friends seen in oncology clinics, and a verbal telephone version for Cancer Information Service callers. We tested for correlations between CCT awareness and SB37 knowledge, and willingness to participate in CCTs. Results Of 1,188 respondents, 59% were aware of CCTs, 19% knew of SB37, and 36% were very likely to consider a CCT. There were significant positive correlations between CCT awareness and willingness to participate (P < .001, Spearman), and between SB37 knowledge and willingness to participate (P = .001, Pearson χ2). Reduced awareness was seen in respondents who were either black or African American (odds ratio [OR], 0.44; P = .004), Hispanic (OR, 0.56; P = .03), had an annual income less than $25,000 (OR, 0.38; P < .001), or had less than a college degree (OR, 0.12 to 0.53; P < .001 to .013). Reduced willingness to participate in CCTs was seen in black or African American participants (OR, 0.38; P < .001), Asians (OR, 0.44; P < .006), or respondents aged 18 to 24 years (OR, 0.35; P = .002). Conclusion These results support the hypothesis that improving CCT awareness and SB37 knowledge especially among lower income, less educated, and minority patients, may potentially overcome barriers to participation and subsequently increase accrual in California.

2011 ◽  
pp. 2261-2275
Author(s):  
J. David Johnson

The Cancer Information Service is a knowledge management organization, charged with delivering information to the public concerning cancer. This chapter describes how societal trends in consumer/client information behavior impact clinical knowledge management. It then details how the CIS is organized to serve clients and how it can interface with clinical practice by providing referral, by enhancing health literacy, by providing a second opinion, and by giving crucial background, assurance to clients from neutral third party. The CIS serves as a critical knowledge broker, synthesizing and translating information for clients before, during, and after their interactions with clinical practices; thus enabling health professionals to focus on their unique functions.


2010 ◽  
Vol 25 (2) ◽  
pp. 142-145 ◽  
Author(s):  
Georgia Robins Sadler ◽  
Jenny Gonzalez ◽  
Manpreet Mumman ◽  
Lisa Cullen ◽  
Sheila F. LaHousse ◽  
...  

2014 ◽  
Vol 3 (5) ◽  
pp. 1430-1439 ◽  
Author(s):  
Lindsey Haynes‐Maslow ◽  
Paul Godley ◽  
Lisa Dimartino ◽  
Brandolyn White ◽  
Janice Odom ◽  
...  

2011 ◽  
Vol 37 (2) ◽  
pp. 335-343 ◽  
Author(s):  
Sherrie Flynt Wallington ◽  
Gheorghe Luta ◽  
Anne-Michelle Noone ◽  
Larisa Caicedo ◽  
Maria Lopez-Class ◽  
...  

2005 ◽  
Vol 23 (22) ◽  
pp. 5247-5254 ◽  
Author(s):  
Worta McCaskill-Stevens ◽  
Martha M. McKinney ◽  
Cynthia G. Whitman ◽  
Lori M. Minasian

Purpose The National Cancer Institute's (NCI) Minority-Based Community Clinical Oncology Program (MBCCOP) seeks to enhance minority participation in cancer clinical trials by building clinical trials outreach and management capacity in healthcare institutions serving large numbers of minority cancer patients. This article examines temporal trends in MBCCOP accruals to cancer prevention and control (CP/C) and cancer treatment trials and the racial distribution of study participants, along with the major factors affecting minority enrollment. Methods We used NCI databases to analyze temporal trends in overall accruals and accruals by race. We analyzed transcripts from an NCI-sponsored meeting with MBCCOP principal investigators and data from a follow-up survey to identify factors affecting minority enrollment. Results Between 1992 and 2003, annual patient accruals to treatment trials increased 39% despite little change in the number of MBCCOP grantees. During this same period, annual participant accruals to CP/C trials more than doubled. Between 1995 and 2003, minorities comprised 51% to 67% of the MBCCOP patients accrued to cooperative group treatment trials compared with ≤ 23% of the patients accrued by other cooperative group members and affiliates. Major factors affecting minority enrollment include the availability of “clinically relevant” protocols, regulatory requirements, characteristics of the patient population, and the level of support from sponsoring institutions and community physicians. Conclusion MBCCOPs have demonstrated their ability to facilitate the participation of racial/ethnic minorities in clinical trials. However, the contributions that they could make to the design and conduct of minority-focused research studies merit further exploration.


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