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Reporting Formative Qualitative Research to Support the Development of Quantitative Preference Study Protocols and Corresponding Survey Instruments: Guidelines for Authors and Reviewers

Author

Listed:
  • Ilene L. Hollin

    (Temple University)

  • Benjamin M. Craig

    (University of South Florida)

  • Joanna Coast

    (University of Bristol)

  • Kathleen Beusterien

    (Kantar)

  • Caroline Vass

    (RTI Health Solutions)

  • Rachael DiSantostefano

    (Janssen R&D, LLC)

  • Holly Peay

    (RTI International)

Abstract

Background Formative qualitative research is foundational to the methodological development process of quantitative health preference research (HPR). Despite its ability to improve the validity of the quantitative evidence, formative qualitative research is underreported. Objective To improve the frequency and quality of reporting, we developed guidelines for reporting this type of research. The guidelines focus on formative qualitative research used to develop robust and acceptable quantitative study protocols and corresponding survey instruments in HPR. Methods In December 2018, a steering committee was formed as a means to accumulate the expertise of the HPR community on the reporting guidelines (21 members, seven countries, multiple settings and disciplines). Using existing guidelines and examples, the committee constructed, revised, and refined the guidelines. The guidelines underwent beta testing by three researchers, and further revisions to the guidelines were made based on their feedback as well as on comments from members of the International Academy of Health Preference Research (IAHPR) and the editorial board of The Patient: Patient-Centered Outcomes Research. Results The guidelines have five components: introductory material (4 domains), methods (12), results/findings (2), discussion (2), and other (2). They are concordant with existing guidelines, published examples, beta-testing results, and expert comments. Conclusions Publishing formative qualitative research is a necessary step toward strengthening the foundation of any quantitative study, enhancing the relevance of its preference evidence. The guidelines should aid researchers, reviewers, and regulatory agencies and promote transparency within HPR more broadly.

Suggested Citation

  • Ilene L. Hollin & Benjamin M. Craig & Joanna Coast & Kathleen Beusterien & Caroline Vass & Rachael DiSantostefano & Holly Peay, 2020. "Reporting Formative Qualitative Research to Support the Development of Quantitative Preference Study Protocols and Corresponding Survey Instruments: Guidelines for Authors and Reviewers," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 13(1), pages 121-136, February.
  • Handle: RePEc:spr:patien:v:13:y:2020:i:1:d:10.1007_s40271-019-00401-x
    DOI: 10.1007/s40271-019-00401-x
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    References listed on IDEAS

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    1. Al-Janabi, Hareth & Coast, Joanna & Flynn, Terry N., 2008. "What do people value when they provide unpaid care for an older person? A meta-ethnography with interview follow-up," Social Science & Medicine, Elsevier, vol. 67(1), pages 111-121, July.
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    3. Vikas Soekhai & Esther W. Bekker-Grob & Alan R. Ellis & Caroline M. Vass, 2019. "Discrete Choice Experiments in Health Economics: Past, Present and Future," PharmacoEconomics, Springer, vol. 37(2), pages 201-226, February.
    4. Louviere, Jordan J. & Lancsar, Emily, 2009. "Choice experiments in health: the good, the bad, the ugly and toward a brighter future," Health Economics, Policy and Law, Cambridge University Press, vol. 4(4), pages 527-546, October.
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    Cited by:

    1. Magda Aguiar & Mark Harrison & Sarah Munro & Tiasha Burch & K. Julia Kaal & Marie Hudson & Nick Bansback & Tracey-Lea Laba, 2021. "Designing Discrete Choice Experiments Using a Patient-Oriented Approach," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(4), pages 389-397, July.
    2. Viberg Johansson, Jennifer & Shah, Nisha & Haraldsdóttir, Eik & Bentzen, Heidi Beate & Coy, Sarah & Kaye, Jane & Mascalzoni, Deborah & Veldwijk, Jorien, 2021. "Governance mechanisms for sharing of health data: An approach towards selecting attributes for complex discrete choice experiment studies," Technology in Society, Elsevier, vol. 66(C).
    3. David J. Mott & Laura Ternent & Luke Vale, 2023. "Do preferences differ based on respondent experience of a health issue and its treatment? A case study using a public health intervention," The European Journal of Health Economics, Springer;Deutsche Gesellschaft für Gesundheitsökonomie (DGGÖ), vol. 24(3), pages 413-423, April.
    4. Xiaoling Ge & Huanhuan Tong & Yongxia Song & Hongye He & Shuwen Li & Jingfang Hong & Wenru Wang, 2020. "The caring experience and supportive care needs of male partners for women with gynaecologic cancer: A qualitative literature review," Journal of Clinical Nursing, John Wiley & Sons, vol. 29(23-24), pages 4469-4481, December.
    5. Stacy M. Carter & Patti Shih & Jane Williams & Chris Degeling & Julie Mooney-Somers, 2021. "Conducting Qualitative Research Online: Challenges and Solutions," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(6), pages 711-718, November.
    6. A. Cecilia Jimenez-Moreno & Eline Overbeeke & Cathy Anne Pinto & Ian Smith & Jenny Sharpe & James Ormrod & Chiara Whichello & Esther W. Bekker-Grob & Kristin Bullok & Bennett Levitan & Isabelle Huys &, 2021. "Patient Preferences in Rare Diseases: A Qualitative Study in Neuromuscular Disorders to Inform a Quantitative Preference Study," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(5), pages 601-612, September.
    7. Merle Gijsbers & Iris Elise Keizer & Stephanie Else Schouten & Janneke Louise Trompert & Catharina G. M. Groothuis-Oudshoorn & Janine Astrid Til, 2021. "Public Preferences in Priority Setting when Admitting Patients to the ICU During the COVID-19 Crisis: A Pilot Study," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(3), pages 331-338, May.
    8. Hareth Al-Janabi & Jenny Coles & John Copping & Nishit Dhanji & Carol McLoughlin & Jacky Murphy & Jean Nicholls, 2021. "Patient and Public Involvement (PPI) in Health Economics Methodology Research: Reflections and Recommendations," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 14(4), pages 421-427, July.
    9. Wiebke Mohr & Anika Rädke & Adel Afi & Franka Mühlichen & Moritz Platen & Annelie Scharf & Bernhard Michalowsky & Wolfgang Hoffmann, 2022. "Development of a Quantitative Preference Instrument for Person-Centered Dementia Care—Stage 2: Insights from a Formative Qualitative Study to Design and Pretest a Dementia-Friendly Analytic Hierarchy ," IJERPH, MDPI, vol. 19(14), pages 1-21, July.
    10. Semra Ozdemir & Jia Jia Lee & Isha Chaudhry & Remee Rose Quintana Ocampo, 2022. "A Systematic Review of Discrete Choice Experiments and Conjoint Analysis on Genetic Testing," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 15(1), pages 39-54, January.
    11. Wiebke Mohr & Anika Rädke & Adel Afi & Franka Mühlichen & Moritz Platen & Bernhard Michalowsky & Wolfgang Hoffmann, 2022. "Development of a Quantitative Instrument to Elicit Patient Preferences for Person-Centered Dementia Care Stage 1: A Formative Qualitative Study to Identify Patient Relevant Criteria for Experimental D," IJERPH, MDPI, vol. 19(13), pages 1-27, June.
    12. Jackson, Louise & Al-Janabi, Hareth & Roberts, Tracy & Ross, Jonthan, 2021. "Exploring young people's preferences for STI screening in the UK: A qualitative study and discrete choice experiment," Social Science & Medicine, Elsevier, vol. 279(C).

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