About this Journal Submit a Manuscript Table of Contents
Nursing Research and Practice

Volume 2014 (2014), Article ID 702683, 13 pages

http://dx.doi.org/10.1155/2014/702683
Research Article

Evaluating the Linguistic Appropriateness and Cultural Sensitivity of a Self-Report System for Spanish-Speaking Patients with Cancer

1University of South Florida, 4202 E Fowler Avenue, Tampa, FL 33620, USA

2University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, MA 02125, USA

3Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA

4University of Central Florida, 4000 Central Florida Boulevard, Orlando, FL 32816, USA

5California Department of State Hospitals, P.O. Box 2297, Vacaville, CA 95696, USA

Received 18 January 2014; Revised 3 June 2014; Accepted 4 June 2014; Published 19 June 2014

Academic Editor: Patsy Yates

Copyright © 2014 Cindy Tofthagen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Spanish speakers in the United States encounter numerous communication barriers during cancer treatment. Communication-focused interventions may help Spanish speakers communicate better with healthcare providers and manage symptoms and quality of life issues (SQOL). For this study, we developed a Spanish version of the electronic self-report assessment for cancer (ESRA-C), a web-based program that helps people with cancer report, track, and manage cancer-related SQOL. Four methods were used to evaluate the Spanish version. Focus groups and cognitive interviews were conducted with 51 Spanish-speaking individuals to elicit feedback. Readability was assessed using the Fry readability formula. The cultural sensitivity assessment tool was applied by three bilingual, bicultural reviewers. Revisions were made to personalize the introduction using a patient story and photos and to simplify language. Focus group participants endorsed changes to the program in a second round of focus groups. Cultural sensitivity of the program was scored unacceptable ( ) for audiovisual material and acceptable ( ) for written material. Fry reading levels ranged from 4th to 10th grade. Findings from this study provide several next steps to refine ESRA-C for Spanish speakers with cancer.

1. Introduction

Hispanics are the fastest growing minority group in the United States (US), currently comprising over 15% of the total population [1]. Approximately, 38% of Hispanics in the United States are Spanish-language dominant and another 38% are bilingual [2]. Hispanics are a diverse group with respect to socioeconomic characteristics, level of acculturation, national origin, and heritage. These factors have all been linked to cancer [3, 4] and other health outcomes [59]. Cancer is the leading cause of death among Hispanics in the US [10]. Spanish-language dominant individuals face barriers to communicating with healthcare providers and have less access to Spanish information, both in print and on the Internet, than do English-speaking patients [11].

The number of Hispanics who utilize the Internet is increasing; however, only 1/3 of Spanish-language dominant Hispanics use the Internet [12]. Hispanics born outside the US, who are older, of lower educational levels, less proficient in English, or of Mexican nationality, are less likely to use the Internet [12]. Hispanics are also more likely to report dissatisfaction with medical care, perhaps because of challenges communicating with healthcare providers [1315].

Studies of cancer treatment-related symptoms in Hispanic patients regularly report higher symptom burden, especially depression and pain [1618]. This may be attributed to culture, family beliefs, and religion (e.g., a stoic attitude toward pain) [19, 20] or physician underestimation of the problem [17, 21, 22]. Poor provider-patient communication adversely impacts the ability of patients to communicate their experiences, understand, and adhere to treatment recommendations [23]. A survey of 624 key opinion leaders around the country, conducted by the National Cancer Institute’s National Hispanic/Latino Cancer Network, identified patient-doctor communication as one of five cancer prevention and control issues of greatest significance to the Hispanic population [24].

Symptoms and quality of life issues (SQOL) are important aspects of cancer and treatment. These SQOL issues can be challenging for patients and healthcare providers to communicate about, even when speaking the same language [25]. Assessment and management of symptoms are fundamental to quality care in oncology, yet emphasis on medical treatments and procedures, time constraints, and perceived lack of effective treatments for SQOL may limit time spent in discussion [26]. The electronic self-report assessment for cancer (ESRA-C) is a web-based program developed to help patients monitor and manage SQOL and communicate more effectively with their healthcare providers [2628]. The program records severity of patient-reported SQOL and provides a summary to clinicians about which SQOL are causing distress. The ESRA-C allows patient users to self-monitor SQOL and receive self-care education and coaching on how to communicate troublesome issues. Two multisite, randomized clinical trials demonstrated that use of ESRA-C increased discussion of distressing SQOL between English-speaking patients with various types of cancer and providers [26] and effectively reduced cancer-related symptom distress, particularly among individuals greater than 50 years old [29].

Family caregivers play an important role in managing cancer-related side effects. Hispanic cultures have long been recognized for collectivistic and multigenerational households where elders are cared for and respected [41]. Personalismo has been described as a core value in Hispanic cultures and places a high value on informal and supportive relationships with others [42]. Similarly, familismo is a core value that emphasizes importance of extended family and a responsibility to care for and support each other. The reliance on family caregivers and the complex challenges they and their caregivers face are important to honor and understand [43]. Because Spanish-speaking patients with cancer cared for in an English-speaking institution are at risk for poor patient-provider communication, we planned a Spanish version of ESRA-C that could be especially useful for Spanish speakers with cancer, helping to bridge the communication gap with healthcare providers, providing information on expected side effects of cancer treatment, and allowing them to monitor and care for changes in SQOL over time. The purpose of this study was to develop a linguistically appropriate and culturally sensitive Spanish version of the electronic self-report assessment for cancer (ESRA-C) with input from Spanish-speaking participants from a variety of backgrounds. We sought to accomplish this by (1) holding focus groups with patients and family caregivers to elicit information about the appeal and cultural sensitivity of ESRA-C Spanish; (2) conducting cognitive interviews with Spanish-speaking participants to identify any issues with readability or cultural sensitivity in the translated instruments; (3) assessing the cultural sensitivity of ESRA-C Spanish using the cultural sensitivity assessment tool (CSAT) [40], a tool that has been used by expert reviewers to evaluate cancer websites; and (4) employing the Fry formula [44, 45] to target the 6th grade reading level recommended for patient education materials in cancer care settings [46].

2. Materials and Methods

2.1. Samples and Settings

Participants in this study were recruited from two sites: Dana-Farber Cancer Institute in Boston, Massachusetts, and a community medical oncology practice with a primarily Hispanic patient population in Tampa, Florida. To be eligible for participation, individuals had to be at the age of 18 or older; Spanish-language-dominant; self-identified Hispanic ethnicity; receiving cancer treatment, a cancer survivor, or a caregiver of someone with cancer. Caregivers were defined for this study as a family member or friend who assists with medical care in any capacity and were included for several reasons: increasing the sample size; importance of family in Hispanic culture; and knowledge of the treatment and experiences of their family member.

Internal Review Board protocol approvals from both the Dana-Farber/Harvard Cancer Center and the University of South Florida were obtained prior to recruitment. In Boston, potential participants were recruited through electronic medical records and also through a Dana-Farber Latino Patient and Caregiver conference. Interested conference attendees were asked to provide contact information. Potentially eligible patients were mailed an invitation letter with an opt-out response form. A research assistant telephoned patients who did not opt out. The study staff obtained approval for participation from patients’ oncology providers. Patients were given the opportunity to ask a caregiver to participate. In Tampa, eligible participants were identified and referred to the study by the oncologist and then contacted by study staff to determine interest in participation and obtain consent.

2.2. Key Informant Panel Meetings

The study team met three times with a key informant panel from the Dana-Farber interpreter, patient navigator, social work, and outreach services. These four bilingual, Hispanic panel members reviewed the existing English ESRA-C website and provided suggestions for focus group discussion and enhancements to ESRA-C. The study team implemented the panel’s recommendations prior to the first round of focus groups by (1) adding information about members of the healthcare team and respective roles; (2) using photographs to illustrate interaction with the care team; and (3) adding pop-up definitions to assist lower literacy patients in understanding terminology on the website. The panel also recommended study of participant understanding of questionnaire items and responses that are included in ESRA-C. Suggestions by the panel that were outside the scope of our study, and thus not addressed, included animated or video introduction to cancer treatment modalities and integration with electronic medical records and patient portal.

2.3. Focus Groups

The study team prepared a mock website for participants’ review with new content and graphics (photographs of patients, computer users, and healthcare providers). A professional healthcare translation/interpretation company translated the mock website to Spanish. Focus groups were conducted to explore participants’ previous experiences communicating about symptoms and quality of life issues, Internet use, and overall interest in electronic SQOL reporting and education. Participants were asked to evaluate the mock website for cultural sensitivity and appropriateness of terminology.

We planned to hold one initial focus group in Boston and two in Tampa. Instead, we conducted two initial focus groups in Boston and one in Tampa due to difficulty with recruitment in Tampa. Focus group meetings were conducted using an interview guide with specific open-ended questions that began with discussion of patient/caregiver experiences and moved to discussion of the mock website (Table 1). Bilingual, bicultural facilitators (authors Laura Gonzalez, Veronica Sanchez Varela, and Rosalyn Negrón) led the focus groups. Members of the study team observed and took notes; sessions were audio recorded and then transcribed and translated into English. The research team reviewed the transcripts, discussed all suggestions and recommendations, and prioritized revisions for implementation.

tab1
Table 1: Focus group interview topics and prompts.

Focus groups were reconvened to evaluate the revisions and provide further feedback. A summary of the recommendations from the first round of review was presented to the reconvened groups and the revised ESRA-C was reviewed. Participants were asked to confirm that all of the recommended changes were implemented to their satisfaction and to provide additional suggestions.

2.4. Cognitive Interviews

Based on the suggestions of the key informant panel, a series of 36 cognitive interviews were conducted in Boston to assess understanding and ability to complete symptom and quality of life questionnaires included in ESRA-C. Patients, not caregivers, were invited to participate in cognitive interviews. Cognitive interviewing [47] was selected because it is a useful technique for evaluating health related educational materials and survey questions. Cognitive interviewing encourages participants to discuss how they arrive at responses, reflect on their interpretation of each question and response option, and discuss any problem they have in responding [47].

During audio-recorded individual interviews, patients were asked to evaluate SQOL questionnaires in Spanish using the “think aloud” method and interview probes. Existing Spanish translations of the questionnaires were used when they were available and others were translated into Spanish by professional translators for use in this study. The “think aloud” method was used because open-ended questions minimize the impact of interviewer imposed bias and interviewer probing allows for deeper insight into individual responses [48]. Participants were asked to discuss whether questions, vocabulary, and context were easily understood and make suggestions for revision. All interviews were conducted in a private room within the cancer center. The research assistant conducting the interviews also took written notes. Participants provided feedback on as many of the questionnaires as relevant to their diagnosis, disease status, and treatment history.

2.5. Cultural Sensitivity

Cultural Sensitivity Assessment Tool. Following the focus groups and cognitive interviews, final revisions were made to the mock website. The cultural sensitivity assessment tool (CSAT) [49] was then used as a formal measure of cultural sensitivity. The CSAT was originally developed to assess cancer education materials for African Americans. In this tool, cultural sensitivity has been defined as “an awareness and utilization of knowledge related to ethnicity, culture, gender, or sexual orientation in explaining and understanding situations and responses of individuals in their environment” [50]. When applied to evaluation of health related materials, it means that the message and content (1) is understandable to the intended audience, (2) reflects understanding of the cultural context of behavior, and (3) is congruent with cultural norms [51].

A document containing all Spanish ESRA-C assessment items and educational text along with the mock website URL was provided to three reviewers external to the study team who applied the CSAT. The reviewers were bilingual, bicultural professionals. Two reviewers, who were employed as patient navigators for Hispanic patients, had also participated in the key informant panel. The third reviewer was employed in a Hispanic community as a child and family welfare officer.

The CSAT is comprised of two evaluation sets, one for print and one for audiovisual (AV) material. We adapted the CSAT, drawing from both versions, to assess cultural sensitivity of a cancer education website with both text and audiovisual components for Hispanic users. Our final version included 56 items in three categories: format (7 AV items; e.g., the audiovisual medium is appropriate for the intended audience); written/verbal message (11 print items, 11 AV items; e.g., the medical terms used in the verbal message are understandable to the intended audience); and visual message (11 print items, 16 AV items; e.g., the visuals illustrate contemporary activities of the intended audience), with each Likert-type item ranging from 4 (strongly agree that the information is culturally sensitive) to 1 (strongly disagree). Each category’s scores were averaged across items and reviewers. Scores were tabulated and compared to acceptable benchmarks set by the CSAT authors [49] of 3.3 for audiovisual and 2.5 for written material categories.

2.6. Readability

The Fry Readability Formula. The Fry readability formula is a widely recognized formula for assessing readability of both English and Spanish materials and has been validated in both languages [52]. The Fry formula is especially useful in evaluating Spanish reading materials, because it takes into account the structure of the Spanish language, allowing for more polysyllabic words than English materials at the same reading level [45]. Following instructions for applying the formula, the study team selected three, 100-word passages for scoring from the three sections of educational text in the final Spanish mock website/content document: Meet Your Care Team (Conozca a los miembros de su equipo médico), which introduces patients to the roles of various healthcare professionals in an oncology setting; Getting Help (Cómo obtener ayuda), which coaches patients to engage in self-care for symptom and quality of life issues and to communicate problems to their providers; and What can I do about fatigue? (¿Qué puedo hacer al respecto la fatiga (mucho cansancio)?), an activity-based intervention for cancer-related fatigue. Average numbers of sentences and syllables were derived for each section and plotted on the Fry graph to obtain reading levels.

2.7. Data Analysis

Descriptive statistics were used to evaluate demographic characteristics of participants. The anonymous focus group data were entered into a code-based data analysis software package (Atlas.ti). Members of the study team independently listened to focus group audio recordings, read observer notes, and reviewed English transcripts of each focus group. Bilingual research team members also reviewed the Spanish transcripts. Transcripts were analyzed to determine necessary revisions to ESRA-C that would improve cultural sensitivity and linguistic appropriateness. CSAT scores were reviewed and low scoring items identified. Fry readability levels were reviewed and areas scoring above a 6th grade level identified.

3. Results

3.1. Sample

Two initial focus groups were held in Boston, but recruitment in Tampa only filled one group. Following revisions to ESRA-C, two groups were reconvened in Boston and a new group was convened in Tampa. Individual interviews were also held with patients in Boston. A total of 51 individuals, 32 women and 19 men, participated in the study (Table 2). Approximately half of the participants in the study were from the Dominican Republic with the remaining reporting Puerto Rican, Cuban, Salvadoran, Guatemalan, Colombian, Ecuadorian, or Chilean heritage. Ages ranged from 32 to 86 with a mean age of 61 years.

tab2
Table 2: Demographic characteristics and participant activity ( ).
3.2. Focus Group Results

Initial Focus Group Meetings. Participants described language related barriers to effective communication, including apprehension about saying things correctly in English, frustration when communication is difficult, and the need to rely on family members or professional interpreters to aid communication. Participants expressed the need to speak to their physician by telephone and shared frustrations about not being able to use the telephone to communicate because of language barriers. In spite of difficulties with communication, participants consistently offered praise for healthcare providers.

The patients described using the Internet to obtain general health information and to access personal medical records. They often relied on caregivers and family members to access the Internet and retrieve information. Typical access to the Internet was on a home computer rather than on a mobile device. Participants discussed use of the Internet for maintaining contact and socializing with others and some described how social media was used to update loved ones regarding their condition. Sharing information about cancer experiences with others via social media was described as a way to help others who may be going through similar experiences. The importance of being able to provide emotional support to others, as well as receive emotional support from family and friends, was a recurrent topic. Spirituality and faith in God were important coping strategies reported by participants. Participants reported that ESRA-C would be useful for helping patients know what to expect during cancer treatment. The following quotes are demonstrative of how participants perceived ESRA-C to be useful during cancer treatment.

“I think this (ESRA-C) is a way to help people express what they feel and inform the doctor when they see him, to understand what’s going on…because it is easier to express in writing all those concerns or feelings you have inside. This is a way to help communication.”

“It is wonderful what you are doing, it is so necessary because at any time of the day, you could sit in front of this computer and express what you’re feeling, at that moment!”

“We are entering into a path, into a sort of dark tunnel without knowing anything but in this case…you can understand, and you are able to write it down.”

Most participants stated that the list of symptom and quality of life issues was easy to understand. Suggestions for revision included adding specific skin-related symptoms such as dry skin and burns, adding more emotional descriptors (bad mood, tranquility), expanding definitions, and eliminating difficult-to-understand terminology. Some participants reported difficulty with reporting pain on a 0–10 scale and suggested the use of smiling or frowning faces as a gauge of pain levels. Some participants voiced misunderstanding one questionnaire’s response option that read, “more than half the days” (of a week).

Perceived potential benefits of ESRA-C Spanish included improved patient-physician communication, ability to instantly report symptoms, and ability to anonymously report and receive information on subjects of a sensitive nature, such as depression and sexuality. Perceived potential barriers included concerns that the information from ESRA-C Spanish would not be communicated to doctors. Participants were concerned that some of the medical terminology, such as the words fatigue and palliative care, may be difficult for all patients to understand.

Participants in the initial three focus groups identified numerous areas for revisions to ESRA-C (Table 3). Participants expressed a strong preference for the content to be presented using first-person language, incorporating patient photographs, voices, and testimonials. The mock website was revised to include narration and presentation of content from a patient perspective. We also revised the text content to reflect suggested changes, revised the layout to further emphasize the main subject on each page with larger and bolder fonts, streamlined navigational elements, and added screenshots of the ESRA-C website to the narrated patient story to illustrate how to use the program.

tab3
Table 3: Qualitative analysis of focus group transcripts: topics, themes, and concepts.

Reconvening the Focus Groups. After suggestions from the initial focus groups were reviewed and revisions were made to the mock ESRA-C website, participants were invited back for a second meeting to evaluate the changes and make further recommendations. The participants in the second focus group in Tampa had not participated in the initial focus group because previous participants could not be contacted or were no longer available. All groups were provided with an overview of the revisions and presented with a mock-up of the revised version. Participants reported satisfaction with the revisions. They commented positively on the new patient-led narration, stating that the narrator was easy to relate to and encouraging and that the narrator gave important information about communicating symptoms to the clinical team. Further suggestions for revisions included adding information on nutrition, prevalence of symptoms, prevalence of cancer, and what to expect from chemotherapy and radiation therapy. Participants recommended that the program emphasize that every person’s experience is unique.

3.3. Cognitive Interview Results

Analyses of individual interview responses (Table 4) indicate that participants had little difficulty with most items in most instruments. Participants identified specific issues with understanding terminology and had difficulty understanding response options for select items and questionnaires.

tab4
Table 4: Cognitive interview results: instruments, items, number participants per instrument, and issues.
3.4. CSAT Results

Average scores for the two print materials categories of the CSAT ( = 3.2 across reviewers for written message, 2.9 for visual message) exceeded the minimum scores (2.5 of 4) recommended by the CSAT authors for acceptability [53]. Among the categories for audiovisual materials, the average scores in all three categories (3.0 for format, 3.1 for verbal message, 2.9 for visual message) fell below the recommended level of 3.3. Comments from the reviewers indicated that the lowest scores, related to visual message, were because one proxy patient presented in photos and voiceover could not represent the possible diversity of appearance (e.g., in skin color and face shape) of target users (Table 5). One reviewer stated “There is not one common physical feature for Latinos. We’re a racially diverse group so that should be represented.” Most of the additional comments from reviewers ( ) suggested minor wording changes to questions in validated questionnaire translations or to educational text, such as the simpler word debilidad instead of extenuación in an item assessing fatigue.

tab5
Table 5: Individual items with low scores (1 or 2) in the cultural sensitivity assessment tool (CSAT).
3.5. Readability Results

The Meet Your Care Team content was scored at a 10th grade reading level. The Getting Help content was scored at a 4th grade, and the Fatigue Activity Intervention content was scored at a 6th grade reading level. We were able to achieve the targeted 6th grade reading level for cancer education materials in those sections of ESRA-C Spanish in which we engaged the expertise of a health communication writer. This writer revised the English text prior to translation and focused on enhancing readability through both lower reading level (as measured by readability formulas) and other factors such as chunking and bulleting text and formatting it with white space. The Meet Your Care Team section was developed last, and due to time constraints during the study we did not engage the involvement of the health communication writer. It had the highest reading level of all text scored.

3.6. Revisions to ESRA-C

Changes were made to ESRA-C as a result of key informant panel review, both sets of focus groups, and cognitive interviews. Table 6 presents a summary of these changes and how each was evaluated. All suggestions made by participants or key informant panel member were considered by the research team and changes were made consistent with improving communication with healthcare providers, providing information on expected side effects of cancer treatment, and allowing patients to monitor changes in SQOL over time. Some suggestions from focus groups (e.g., newsletter, moderated chat) that were not in direct alignment with the goals of ESRA-C or which exceeded available resources were not implemented.

tab6
Table 6: Suggestions from key informants, focus group and cognitive interview participants, and study team members with resulting revisions and revision evaluation procedures.

4. Discussion

In this study of the iterative content development of a web-based symptom and quality of life assessment and support intervention (ESRA-C) for Spanish-speaking patients with cancer, we found that patients, family caregivers, and professionals who work with them (key informant panel members) generally endorsed the concept and content of ESRA-C. When concerns about Internet access and acceptability were raised, most patients and caregivers indicated they would be able to use ESRA-C, with assistance from family members, if needed.

Other studies have also demonstrated similar preferences for Spanish language educational materials to be presented from a personal perspective with attention to family and spirituality as important cultural values. Consistent with our findings, others have described participants’ privacy concerns with professional translators [54]. Researchers from Moffitt Cancer Center explored possible ways to increase Hispanic participation in clinical trials and also found preferences for the use of patient stories and experiences, depiction of family, and inclusion of elements representing spirituality such as a graphic depicting a family in prayer [55]. In a study adapting a colorectal cancer screening decision aid for Spanish-speaking Latinos, focus group participants stated a preference for personalism (personalismo) in having a patient character, rather than an anonymous narrator, be a guide to the medical information [56]. Others have described the importance of integrating these values into the care of Hispanics receiving palliative care [42], and our findings support the need to affirm and acknowledge these values across treatment settings and integrate them into patient education.

As in Ko and colleagues’ work [56], we followed an iterative process to adapt an English-language web-based program in a way that preserves the benefits of the original intervention but adds cultural specificity, going beyond simple translation. We found that, in addition to patient/caregiver participation, input from a key informant panel of patient navigators and interpreters prior to the focus groups and formal evaluation of a mock website by expert reviewers identified aspects of cultural appropriateness and useful content complementary to that provided by patients/caregivers.

Application of the CSAT and Fry readability formula were considered necessary strategies for formally identifying issues of cultural appropriateness and usability. In a CSAT evaluation of a web-based prostate cancer prevention education program [40], average score for written messages (3.28, range 3.20–3.37) was comparable to the score for the Spanish ESRA-C (3.15), while average scores for visual message (1.36, range 0.96–1.76) were considerably lower than those for Spanish ESRA-C. A study of cancer-related educational materials distributed by the New Jersey Health Department [57] indicated that half of the materials used by the Department received scores at or below the acceptable value of 2.5 in one or more categories of the CSAT. Using the Fry readability formula, almost all of the materials (93%) were written at a level beyond the recommended 6th grade reading level.

4.1. Limitations

Due to convenience sampling of patients/caregivers from two institutions in Boston and Tampa and recruitment challenges in Tampa, most participants came from Boston and are not representatives of all Spanish-dominant cancer patients in the US. Over half of our participants were Dominicans, which is more reflective of the Hispanic population of Boston than the US as a whole [58]. Conversely, no persons of Mexican heritage participated in our study, although the majority of Hispanics in the US are of Mexican heritage [59].

Even though participants in this study reported being able to access the Internet, our sample may not be representative of other Spanish-speaking groups in the US. Internet use among Hispanics, particularly those who are Spanish-dominant, has been reported to be lower [12, 60] than what participants in our study described. Some of the participants did not access the Internet themselves, but instead younger family members accessed medical information from the Internet and passed it on to the older patients. This is consistent with studies showing that Hispanics of older age are less likely to use the Internet themselves [61].

Our measures of cultural appropriateness and reading level were limited. The CSAT was developed in the 1990s, one version for print and another for audiovisual materials. Neither instrument adequately measures interactive websites. It is widely acknowledged that aspects of medium and formatting affect readability, but tools assessing these factors are in development stages or not yet validated [6264].

4.2. Future Research

In future studies, we will revise the website to include photos and voiceovers with a variety of patient characteristics, incorporate a moderated chat feature, and add a guided tour of how to use the website. We plan to include more resources for caregivers into ESRA-C. Research indicates that family preferences heavily influence treatment decisions, particularly in less acculturated Hispanics [65]. To address readability and appropriate wording, we will examine feedback from reviewers, engage a health communication writer in revising or developing new content, and reassess our choice of symptom instruments and external website links. We will incorporate resources specifically for caregivers and expand messaging on the diagnosis of cancer to address participants’ concerns that newly diagnosed patients and others around them may view cancer as a death sentence.

5. Conclusions

The findings from this study provide beginning evidence that ESRA-C Spanish program will provide understandable and relevant information to Spanish-speaking patients with cancer and their caregivers. Assessment of cultural sensitivity supported acceptable levels of sensitivity and provided information about aspects of the intervention that could be refined to enhance cultural sensitivity. Our results provide important next steps for development of the ESRA-C Spanish program.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

Funding is provided by Oncology Nursing Society Foundation/Sigma Theta Tau International. The authors would also like to acknowledge Taylor Hendel for paper preparation and the following research assistants and students who worked on this project: Briseyda Vega, Rosa Mejia, Laura Ardila, and Sindy Ortiz Pimentel.

References

  1. R. Bernstein, U.S. Hispanic Population Surpasses 45 Million-Now 15 Percent of Total U.S.C. Bureau, US Deartment of Commerce, Washington, DC, USA, 2008.
  2. J. Martínez and G. Velasco, Pew Research Hispanic Trends Project: Language Use among Latinos, 2012, http://www.pewhispanic.org/2012/04/04/iv-language-use-among-latinos.
  3. A. G. Ramirez, G. A. Talavera, R. Villarreal et al., “Breast cancer screening in regional hispanic populations,” Health Education Research, vol. 15, no. 5, pp. 559–568, 2000. View at Scopus
  4. R. E. Zambrana, N. Breen, S. A. Fox, and M. L. Gutierrez-Mohamed, “Use of cancer screening practices by Hispanic women: analyses by subgroup,” Preventive Medicine, vol. 29, no. 6, part I, pp. 466–477, 1999. View at Publisher · View at Google Scholar · View at Scopus
  5. D. A. Savitz, T. M. Janevic, S. M. Engel, J. S. Kaufman, and A. H. Herring, “Ethnicity and gestational diabetes in New York City, 1995–2003,” BJOG, vol. 115, no. 8, pp. 969–978, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. L. N. Borrell and N. D. Crawford, “Disparities in self-reported hypertension in Hispanic subgroups, non-Hispanic black and non-Hispanic white adults: the national health interview survey,” Annals of Epidemiology, vol. 18, no. 10, pp. 803–812, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. J. V. Bowie, H.-S. Juon, J. Cho, and E. M. Rodriguez, “Factors associated with overweight and obesity among Mexican Americans and Central Americans: results from the 2001 California Health Interview Survey,” Preventing Chronic Disease, vol. 4, no. 1, p. A10, 2007. View at Scopus
  8. M. A. Oquendo, D. Lizardi, S. Greenwald, M. M. Weissman, and J. J. Mann, “Rates of lifetime suicide attempt and rates of lifetime major depression in different ethnic groups in the United States,” Acta Psychiatrica Scandinavica, vol. 110, no. 6, pp. 446–451, 2004. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Alegría, G. Canino, P. E. Shrout et al., “Prevalence of mental illness in immigrant and non-immigrant U.S. Latino groups,” American Journal of Psychiatry, vol. 165, no. 3, pp. 359–369, 2008. View at Publisher · View at Google Scholar · View at Scopus
  10. American Cancer Society, Cancer Facts & Figures for Hispanics/Latinos 2012–2014, 2012.
  11. J. Alexander, H. T. Kwon, R. Strecher, and J. Bartholomew, “Multicultural media outreach: increasing cancer information coverage in minority communities,” Journal of Cancer Education, vol. 28, no. 4, pp. 744–747, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. S. Fox and G. Livinston, Latinos online: hispanics with lower levels of education and English proficiency remain largely disconnected from the internet, 2007.
  13. J. Z. Ayanian, A. M. Zaslavsky, E. Guadagnoli et al., “Patients' perceptions of quality of care for colorectal cancer by race, ethnicity, and language,” Journal of Clinical Oncology, vol. 23, no. 27, pp. 6576–6586, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. L. S. Morales, W. E. Cunningham, J. A. Brown, H. Liu, and R. D. Hays, “Are Latinos less satisfied with communication by health care providers?” Journal of General Internal Medicine, vol. 14, no. 7, pp. 409–417, 1999. View at Publisher · View at Google Scholar · View at Scopus
  15. J. Z. Ayanian, A. M. Zaslavsky, N. K. Arora et al., “Patients' experiences with care for lung cancer and colorectal cancer: findings from the cancer care outcomes research and surveillance consortium,” Journal of Clinical Oncology, vol. 28, no. 27, pp. 4154–4161, 2010. View at Publisher · View at Google Scholar · View at Scopus
  16. R. Eversley, D. Estrin, S. Dibble, L. Wardlaw, M. Pedrosa, and W. Favila-Penney, “Post-treatment symptoms among ethnic minority breast cancer survivors,” Oncology Nursing Forum, vol. 32, no. 2, pp. 250–256, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. K. T. Ashing-Giwa, G. V. Padilla, D. E. Bohórquez, J. S. Tejero, and M. Garcia, “Understanding the bre0ast cancer experience of Latina women,” Journal of Psychosocial Oncology, vol. 24, no. 3, pp. 19–52, 2006. View at Publisher · View at Google Scholar · View at Scopus
  18. K. M. Christie, B. E. Meyerowitz, and R. C. Maly, “Depression and sexual adjustment following breast cancer in low-income Hispanic and non-Hispanic White women,” Psycho-Oncology, vol. 19, no. 10, pp. 1069–1077, 2010. View at Publisher · View at Google Scholar · View at Scopus
  19. G. Juarez, B. Ferrell, and T. Borneman, “Influence of culture on cancer pain management in hispanic patients,” Cancer Practice, vol. 6, no. 5, pp. 262–269, 1998. View at Publisher · View at Google Scholar · View at Scopus
  20. K. O. Anderson, C. R. Green, and R. Payne, “Racial and ethnic disparities in pain: causes and consequences of unequal care,” Journal of Pain, vol. 10, no. 12, pp. 1187–1204, 2009. View at Publisher · View at Google Scholar · View at Scopus
  21. K. O. Anderson, T. R. Mendoza, R. Payne et al., “Pain education for underserved minority cancer patients: a randomized controlled trial,” Journal of Clinical Oncology, vol. 22, no. 24, pp. 4918–4925, 2004. View at Publisher · View at Google Scholar · View at Scopus
  22. R. C. Maly, Y. Liu, B. Leake, A. Thind, and A. L. Diamant, “Treatment-related symptoms among underserved women with breast cancer: the impact of physician-patient communication,” Breast Cancer Research and Treatment, vol. 119, no. 3, pp. 707–716, 2010. View at Publisher · View at Google Scholar · View at Scopus
  23. J. E. Nelson, E. B. Gay, A. R. Berman, C. A. Powell, J. Salazar-Schicchi, and J. P. Wisnivesky, “Patients rate physician communication about lung cancer,” Cancer, vol. 117, no. 22, pp. 5212–5220, 2011. View at Publisher · View at Google Scholar · View at Scopus
  24. A. G. Ramirez, K. J. Gallion, L. Suarez et al., “A national agenda for Latino cancer prevention and control,” Cancer, vol. 103, no. 11, pp. 2209–2215, 2005. View at Publisher · View at Google Scholar · View at Scopus
  25. S. M. Dy, S. M. Harman, U. K. Braun, L. J. Howie, P. F. Harris, and R. L. Jayes, “To stent or not to stent: an evidence-based approach to palliative procedures at the end of life,” Journal of Pain and Symptom Management, vol. 43, no. 4, pp. 795–801, 2012. View at Publisher · View at Google Scholar · View at Scopus
  26. D. L. Berry, B. A. Blumenstein, B. Halpenny et al., “Enhancing patient-provider communication with the electronic self-report assessment for cancer: a randomized trial,” Journal of Clinical Oncology, vol. 29, no. 8, pp. 1029–1035, 2011. View at Publisher · View at Google Scholar · View at Scopus
  27. D. L. Berry, L. J. Trigg, W. B. Lober et al., “Computerized symptom and quality-of-life assessment for patients with cancer part I: development and pilot testing,” Oncology Nursing Forum, vol. 31, no. 5, pp. 75–83, 2004. View at Scopus
  28. B. T. Karras, S. Wolpin, W. B. Lober, N. Bush, J. R. Fann, and D. L. Berry, “Electronic Self-report Assessment—Cancer (ESRA-C): working towards an integrated survey system,” Studies in Health Technology and Informatics, vol. 122, pp. 514–518, 2006. View at Scopus
  29. D. L. Berry, F. Hong, J. R. Fann, et al., “Electronic self-report assessment for cancer and self-care support: results of a multicenter randomized trial,” Journal of Clinical Oncology, vol. 32, no. 3, pp. 199–205, 2013. View at Publisher · View at Google Scholar
  30. N. K. Aaronson, S. Ahinedzai, B. Bergman et al., “The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology,” Journal of the National Cancer Institute, vol. 85, no. 5, pp. 365–376, 1993. View at Scopus
  31. T. J. Postma, N. K. Aaronson, J. J. Heimans et al., “The development of an EORTC quality of life questionnaire to assess chemotherapy-induced peripheral neuropathy: the QLQ-CIPN20,” European Journal of Cancer, vol. 41, no. 8, pp. 1135–1139, 2005. View at Publisher · View at Google Scholar · View at Scopus
  32. D. Amtmann, K. F. Cook, M. P. Jensen et al., “Development of a PROMIS item bank to measure pain interference,” Pain, vol. 150, no. 1, pp. 173–182, 2010. View at Publisher · View at Google Scholar · View at Scopus
  33. National Institutes of Health, Patient-Reported Outcomes Measurement Information System (PROMIS) ADULT PAIN INTERFERENCE PROFILE SHORT FORMS A brief guide to the 4-item PROMIS Short Form v1.0-Pain Interference 4a, the 6-item PROMIS.
  34. National Institutes of Health, Patient-Reported Outcomes Measurement Information System (PROMIS) ADULT FATIGUE VERSION 1.0 SHORT FORM. A brief guide to the 7-item PROMIS Short Form v1.0-Fatigue 7a.
  35. National Institutes of Health, Patient-Reported Outcomes Measurement Information System (PROMIS) ADULT DEPRESSION. A brief guide to the PROMIS Depression instruments.
  36. P. Chang, K. M. Szymanski, R. L. Dunn et al., “Expanded prostate cancer index composite for clinical practice: development and validation of a practical health related quality of life instrument for use in the routine clinical care of patients with prostate cancer,” Journal of Urology, vol. 186, no. 3, pp. 865–872, 2011. View at Publisher · View at Google Scholar · View at Scopus
  37. R. McCorkle and K. Young, “Development of a symptom distress scale,” Cancer Nursing, vol. 1, no. 5, pp. 373–378, 1978. View at Scopus
  38. K. Kroenke, R. L. Spitzer, and J. B. W. Williams, “The PHQ-9: validity of a brief depression severity measure,” Journal of General Internal Medicine, vol. 16, no. 9, pp. 606–613, 2001. View at Publisher · View at Google Scholar · View at Scopus
  39. R. L. Spitzer, K. Kroenke, and J. B. W. Williams, “Validation and utility of a self-report version of PRIME-MD: the PHQ Primary Care Study,” Journal of the American Medical Association, vol. 282, no. 18, pp. 1737–1744, 1999. View at Publisher · View at Google Scholar · View at Scopus
  40. D. B. Friedman and E. K. Kao, “A comprehensive assessment of the difficulty level and cultural sensitivity of online cancer prevention resources for older minority men,” Preventing Chronic Disease, vol. 5, no. 1, p. A07, 2008. View at Scopus
  41. M. E. Ruiz, “Familismo and filial piety among Latino and Asian elders: reevaluating family and social support,” Hispanic Health Care International, vol. 5, no. 2, pp. 81–89, 2007. View at Publisher · View at Google Scholar · View at Scopus
  42. H. Y. Adames, S. P. Salas, N. Y. Chavez-Duenas, et al., “Integration of Latino/a cultural values into palliative health care: a culture centered model,” Palliative and Supportive Care, vol. 12, no. 2, pp. 149–157, 2014. View at Publisher · View at Google Scholar
  43. C. Gelman, “Familismo and its impact on the family caregiving of Latinos with Alzheimers Disease: a complex narrative,” Research on Aging, vol. 36, no. 1, pp. 40–71, 2014.
  44. E. Fry, “A readibility formula that saves time,” Journal of Reading, vol. 11, no. 7, pp. 513–516, 1968.
  45. D. B. Friedman and L. Hoffman-Goetz, “A systematic review of readability and comprehension instruments used for print and web-based cancer information,” Health Education and Behavior, vol. 33, no. 3, pp. 352–373, 2006. View at Publisher · View at Google Scholar · View at Scopus
  46. C. D. Meade, W. P. McKinney, and G. P. Barnas, “Educating patients with limited literacy skills: the effectiveness of printed and videotaped materials about colon cancer,” American Journal of Public Health, vol. 84, no. 1, pp. 119–121, 1994. View at Scopus
  47. P. C. Beatty and G. B. Willis, “Research synthesis: the practice of cognitive interviewing,” Public Opinion Quarterly, vol. 71, no. 2, pp. 287–311, 2007. View at Publisher · View at Google Scholar · View at Scopus
  48. G. Willis, Cognitive Interviewing: A How-to Guide, 1999, http://fog.its.uiowa.edu/~c07b209/interview.pdf.
  49. D. B. Friedman and L. Hoffman-Goetz, “Assessment of cultural sensitivity of cancer information in ethnic print media,” Journal of Health Communication, vol. 11, no. 4, pp. 425–447, 2006. View at Publisher · View at Google Scholar · View at Scopus
  50. N. C. Facione, “The Triandis model for the study of health and illness behavior: a social behavior theory with sensitivity to diversity,” Advances in Nursing Science, vol. 15, no. 3, pp. 49–58, 1993. View at Scopus
  51. R. Bayer, “AIDS prevention and cultural sensitivity: are they compatible?” American Journal of Public Health, vol. 84, no. 6, pp. 895–898, 1994. View at Scopus
  52. B. Gilliam, S. Pena, and L. R. Moutain, “The fry graph applied to Spanish readability,” Reading Teacher, pp. 426–430, 1980.
  53. J. J. Guidry and V. D. Walker, “Assessing cultural sensitivity in printed cancer materials,” Cancer Practice, vol. 7, no. 6, pp. 291–296, 1999. View at Publisher · View at Google Scholar · View at Scopus
  54. K. Julliard, J. Vivar, C. Delgado, E. Cruz, J. Kabak, and H. Sabers, “What Latina patients don't tell their doctors: a qualitative study,” Annals of Family Medicine, vol. 6, no. 6, pp. 543–549, 2008. View at Publisher · View at Google Scholar · View at Scopus
  55. G. P. Quinn, J. McIntyre, L. E. Gonzalez, T. M. Antonia, P. Antolino, and K. J. Wells, “Improving awareness of cancer clinical trials among hispanic patients and families: audience segmentation decisions for a media intervention,” Journal of Health Communication, vol. 18, no. 9, pp. 1131–1147, 2013. View at Publisher · View at Google Scholar · View at Scopus
  56. L. K. Ko, D. Reuland, R. Clay, et al., “Cultural and linguistic adaptation of a multimedia colorectal cancer screening decision aid for Spanish-speaking latinos,” Journal of Health Communication, vol. 19, no. 2, pp. 192–209, 2014.
  57. P. Pinto, H. Stanley, M. Vega, et al., An Evaluation of Cancer Educational Materials with a Focus on those Currently Distributed by Health Departments in New Jersey, 2005.
  58. E. Roman, Census 2010: hispanics boost Massachusetts population, The Rebublican, 2011.
  59. U. C. Bureau, United States Census 2010, 2010.
  60. C. M. Dang, S. Estrade, C. Bresee, et al., “Exploring potential use of internet, E-mail, and instant text messaging to promote breast health and mammogram use among immigrant Hispanic women in Los Angeles County,” American Surgeon, vol. 79, no. 10, pp. 997–1000, 2013.
  61. A. Gonzalez-Barrera and E. Patten, Closing the Digital Divide: Latinos and Technology Adoption, 2013.
  62. R. A. Goslin and H. A. Elhassan, “Evaluating internet health resources in ear, nose, and throat surgery,” Laryngoscope, vol. 123, no. 7, pp. 1626–1631, 2013. View at Publisher · View at Google Scholar · View at Scopus
  63. K. Ting and A. Hu, “Evaluating the quality and readability of thyroplasty information on the internet,” Journal of Voice, vol. 28, no. 3, pp. 378–381, 2013. View at Publisher · View at Google Scholar
  64. B. Hebert, “Spanish health information resources for nurses,” Pediatric Nursing, vol. 32, no. 4, pp. 350–353, 2006. View at Scopus
  65. R. C. Maly, Y. Umezawa, C. T. Ratliff, and B. Leake, “Racial/ethnic group difference in treatment decision-making and treatment received among older breast carcinoma patients,” Cancer, vol. 106, no. 4, pp. 957–965, 2006. View at Publisher · View at Google Scholar · View at Scopus