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      Comparing two sampling methods to engage hard-to-reach communities in research priority setting

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          Abstract

          Background

          Effective community-partnered and patient-centered outcomes research needs to address community priorities. However, optimal sampling methods to engage stakeholders from hard-to-reach, vulnerable communities to generate research priorities have not been identified.

          Methods

          In two similar rural, largely Hispanic communities, a community advisory board guided recruitment of stakeholders affected by chronic pain using a different method in each community: 1) snowball sampling, a chain- referral method or 2) purposive sampling to recruit diverse stakeholders. In both communities, three groups of stakeholders attended a series of three facilitated meetings to orient, brainstorm, and prioritize ideas (9 meetings/community). Using mixed methods analysis, we compared stakeholder recruitment and retention as well as priorities from both communities’ stakeholders on mean ratings of their ideas based on importance and feasibility for implementation in their community.

          Results

          Of 65 eligible stakeholders in one community recruited by snowball sampling, 55 (85 %) consented, 52 (95 %) attended the first meeting, and 36 (65 %) attended all 3 meetings. In the second community, the purposive sampling method was supplemented by convenience sampling to increase recruitment. Of 69 stakeholders recruited by this combined strategy, 62 (90 %) consented, 36 (58 %) attended the first meeting, and 26 (42 %) attended all 3 meetings. Snowball sampling recruited more Hispanics and disabled persons (all P < 0.05). Despite differing recruitment strategies, stakeholders from the two communities identified largely similar ideas for research, focusing on non-pharmacologic interventions for management of chronic pain. Ratings on importance and feasibility for community implementation differed only on the importance of massage services ( P = 0.045) which was higher for the purposive/convenience sampling group and for city improvements/transportation services ( P = 0.004) which was higher for the snowball sampling group.

          Conclusions

          In each of the two similar hard-to-reach communities, a community advisory board partnered with researchers to implement a different sampling method to recruit stakeholders. The snowball sampling method achieved greater participation with more Hispanics but also more individuals with disabilities than a purposive-convenience sampling method. However, priorities for research on chronic pain from both stakeholder groups were similar. Although utilizing a snowball sampling method appears to be superior, further research is needed on implementation costs and resources.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12874-016-0242-z) contains supplementary material, which is available to authorized users.

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          Most cited references39

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          A systematic review of barriers and facilitators to minority research participation among African Americans, Latinos, Asian Americans, and Pacific Islanders.

          To assess the experienced or perceived barriers and facilitators to health research participation for major US racial/ethnic minority populations, we conducted a systematic review of qualitative and quantitative studies from a search on PubMed and Web of Science from January 2000 to December 2011. With 44 articles included in the review, we found distinct and shared barriers and facilitators. Despite different expressions of mistrust, all groups represented in these studies were willing to participate for altruistic reasons embedded in cultural and community priorities. Greater comparative understanding of barriers and facilitators to racial/ethnic minorities' research participation can improve population-specific recruitment and retention strategies and could better inform future large-scale prospective quantitative and in-depth ethnographic studies.
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            Barriers to recruiting underrepresented populations to cancer clinical trials: a systematic review.

            Racial and ethnic minorities, older adults, rural residents, and individuals of low socioeconomic status are underrepresented among participants in cancer-related trials. The authors conducted a systematic review to determine the barriers to participation of underrepresented populations in cancer-related trials. Their search included English-language publications that reported original data on the recruitment of underrepresented groups to cancer treatment or prevention trials between 1966 and December 2005 in multiple electronic databases. They also hand-searched titles in 34 journals from January 2003 to December 2005 and they examined reference lists for eligible articles. Titles and abstracts were reviewed to identify relevant studies. Data on barriers to participation were synthesized both qualitatively and based on statistically significant associations with trial enrollment. Of 5257 studies that were cited, 65 studies were eligible for inclusion in the current analysis, including 46 studies on recruitment into cancer therapeutic trials, 15 studies on recruitment into prevention trials, and 4 studies on recruitment into both prevention and treatment trials. Numerous factors were reported as barriers to participation in cancer-related trials. However, only 20 of the studies reported statistically significant associations between hypothesized barriers and enrollment. The available evidence had limitations in quality regarding representativeness, justification of study methods, the reliability and validity of data-collection methods, potential for bias, and data analysis. The results indicated that underrepresented populations face numerous barriers to participation in cancer-related trials. The current systematic review highlighting the literature on recruitment of underrepresented populations to cancer trials and may be used as the evidence base toward developing an agenda for etiologic and intervention research to reduce the disparities in participation in cancer-related trials.
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              Mixed Methods Sampling: A Typology With Examples

              C Teddlie, F Yu (2007)
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                Author and article information

                Contributors
                Melissa.A.Valerio@uth.tmc.edu
                RodriguezND@uthscsa.edu
                WinklerP@uthscsa.edu
                Jaime.Lopez@ag.tamu.edu
                Meagen.Dennison@ag.tamu.edu
                LiangY@uthscsa.edu
                210-562-5551 , Turner@uthscsa.edu
                Journal
                BMC Med Res Methodol
                BMC Med Res Methodol
                BMC Medical Research Methodology
                BioMed Central (London )
                1471-2288
                28 October 2016
                28 October 2016
                2016
                : 16
                : 146
                Affiliations
                [1 ]Department of Health Promotion and Behavioral Science, University of Texas School of Public Health in San Antonio, 7411 John Smith Drive, Suite 1100, San Antonio, TX 78229 USA
                [2 ]Center for Research to Advance Community Health (ReACH), University of Texas Health Science Center at San Antonio (UTHSCSA), 7411 John Smith Drive, Suite 1050, San Antonio, TX 78229 USA
                [3 ]South Central Area Health Education Center (AHEC), UTHSCSA, 7411 John Smith Drive, Suite 1050, San Antonio, TX 78229 USA
                [4 ]Frio County AgriLife Extension, 400 S. Pecan Street, Pearsall, TX 78061 USA
                [5 ]Karnes County AgriLife Extension, 115 N. Market Street, Karnes City, TX 78118 USA
                [6 ]Department of Epidemiology and Biostatistics, UTHSCSA, 7703 Floyd Curl Drive, San Antonio, TX 78229 USA
                [7 ]Department of Medicine, UTHSCSA, 7703 Floyd Curl Drive, San Antonio, TX 78229 USA
                Article
                242
                10.1186/s12874-016-0242-z
                5084459
                27793191
                6be8e14e-c5b5-42bd-ab78-1a6f0e6fa7d1
                © The Author(s). 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 July 2016
                : 8 October 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100006093, Patient-Centered Outcomes Research Institute;
                Award ID: ME-13035729
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Medicine
                research methods,sampling studies,vulnerable populations,chronic pain,community-based participatory research

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