Literature DB >> 19012066

Methodological challenges in quality of life research among Turkish and Moroccan ethnic minority cancer patients: translation, recruitment and ethical issues.

Rianne Hoopman1, Caroline B Terwee, Martin J Muller, Ferko G Ory, Neil K Aaronson.   

Abstract

The large population of first generation Turkish and Moroccan immigrants who moved to Western Europe in the 1960s and 1970s is now reaching an age at which the incidence of chronic diseases, including cancer, rises sharply. To date, little attention has been paid to the health-related quality of life (HRQOL) of these ethnic minority groups, primarily due to the paucity of well translated and validated measures, but also because of a range of methodological and logistical barriers. The primary objective of this paper is to describe the methodological challenges in conducting HRQOL research among these patient populations, based on experience gained in a project in which four widely used HRQOL questionnaires were translated into Turkish, Moroccan-Arabic and Tarifit, and administered to a sample of 90 Turkish and 79 Moroccan cancer patients in the Netherlands. Problems encountered in translating and administering the questionnaires included achieving semantic equivalence (use of loanwords), use of numerical rating scales, lengthy questions and response scales, and culturally sensitive and/or inappropriate questions. Privacy laws that prohibit hospitals from registering the ethnicity of patients hampered efficient identification of eligible patients. Recruiting patients to studies is often difficult due to low literacy levels, lack of familiarity with and distrust of research, concerns about immigration status, and inaccurate or missing contact information. This can lead to lower response rates than is the case with the population of Dutch cancer patients. Additional ethical issues that arise in such studies concern patients' problems with communicating with their health care providers, their lack of understanding of their diagnosis, treatment and prognosis, and the potential role conflict experienced by bilingual research assistants who may wish or be asked to intervene on the patients' behalf. Practical approaches to resolving these issues are presented.

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Year:  2009        PMID: 19012066     DOI: 10.1080/13557850802398832

Source DB:  PubMed          Journal:  Ethn Health        ISSN: 1355-7858            Impact factor:   2.772


  13 in total

1.  "What Goes Around Comes Around": Attitudes and Practices Regarding Ageing and Care for the Elderly Among Moroccan Muslim Women Living in Antwerp (Belgium).

Authors:  Chaïma Ahaddour; Stef Van den Branden; Bert Broeckaert
Journal:  J Relig Health       Date:  2020-04

2.  Negative health care experiences of immigrant patients: a qualitative study.

Authors:  Jeanine Suurmond; Ellen Uiters; Martine C de Bruijne; Karien Stronks; Marie-Louise Essink-Bot
Journal:  BMC Health Serv Res       Date:  2011-01-14       Impact factor: 2.655

3.  The proxy problem anatomized: child-parent disagreement in health related quality of life reports of chronically ill adolescents.

Authors:  Jane N T Sattoe; AnneLoes van Staa; Henriëtte A Moll
Journal:  Health Qual Life Outcomes       Date:  2012-01-25       Impact factor: 3.186

4.  Personal and environmental factors to consider when aiming to improve participation in physical activity in children with Spina Bifida: a qualitative study.

Authors:  Manon A T Bloemen; Olaf Verschuren; Claudia van Mechelen; Hanneke E Borst; Arina J de Leeuw; Marsha van der Hoef; Janke F de Groot
Journal:  BMC Neurol       Date:  2015-02-10       Impact factor: 2.474

5.  Involving hard-to-reach ethnic minorities in low-budget health research: lessons from a health survey among Moluccans in the Netherlands.

Authors:  Adee J Bodewes; Anton E Kunst
Journal:  BMC Res Notes       Date:  2016-06-21

6.  No common understanding of profession terms utilized in health services research : An add-on qualitative study in the context of the QUALICOPC project in Austria.

Authors:  Kathryn Hoffmann; Silvia Wojczewski; Diederik Aarendonk; Manfred Maier; Thomas Ernst Dorner; Jan de Maeseneer
Journal:  Wien Klin Wochenschr       Date:  2016-12-19       Impact factor: 1.704

7.  Breast cancer genetic counseling among Dutch patients from Turkish and Moroccan descent: participation determinants and perspectives of patients and healthcare professionals.

Authors:  J E Baars; A M van Dulmen; M E Velthuizen; E van Riel; M G E M Ausems
Journal:  J Community Genet       Date:  2017-01-12

8.  A qualitative assessment of implementing a cross-cultural survey on cancer wards in Denmark--a description of barriers.

Authors:  Maria Kristiansen; Amani Hassani; Allan Krasnik
Journal:  BMC Med Res Methodol       Date:  2010-01-12       Impact factor: 4.615

9.  Development and assessment of a verbal response scale for the Patient-Specific Functional Scale (PSFS) in a low-literacy, non-western population.

Authors:  Anupa Pathak; Saurab Sharma; Allen W Heinemann; Paul W Stratford; Daniel Cury Ribeiro; J Haxby Abbott
Journal:  Qual Life Res       Date:  2020-09-23       Impact factor: 3.440

10.  Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.

Authors:  J E Baars; A M van Dulmen; M E Velthuizen; E B M Theunissen; B C Vrouenraets; A N Kimmings; T van Dalen; B van Ooijen; A J Witkamp; M A van der Aa; M G E M Ausems
Journal:  Fam Cancer       Date:  2016-04       Impact factor: 2.375

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