Qualitative understanding of experiences of people with cystic fibrosis in a treatment discontinuation trial: The QUEST study

被引:0
作者
Maggs, Jill
Sawicki, Gregory S.
Bacon, Callie
Mcwilliams, Emma
Yablon, Dana
Ertman, Benjamin
Sweeney, Liam
Butcher, Jennifer L.
Everhart, Robin S.
Prickett, Michelle
Siracusa, Christopher [2 ]
Gifford, Alex H. [3 ,4 ]
Mayer-Hamblett, Nicole [5 ,6 ,7 ]
Nichols, David P. [8 ]
Goodman, Andrea
Woo, Tia
Riekert, Kristin A. [1 ]
机构
[1] Johns Hopkins Univ, Dept Med, Div Pulm & Crit Care Med, 5501 Hopkins Bayview Circle, Baltimore, MD 21224 USA
[2] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[3] Univ Hosp Cleveland Med Ctr, Pulm Crit Care & Sleep Med, Cleveland, OH USA
[4] Rainbow Babies & Childrens Hosp, Cleveland, OH USA
[5] Seattle Childrens Res Inst, Seattle, WA USA
[6] Univ Washington, Dept Pediat, Seattle, WA USA
[7] Univ Washington, Dept Biostat, Seattle, WA USA
[8] Cyst Fibrosis Fdn, Bethesda, MD USA
关键词
Cystic fibrosis; Research participation; Discontinuation trial; THERAPEUTICS DEVELOPMENT NETWORK; CLINICAL-TRIALS; RECRUITMENT; RETENTION; FOUNDATION; INTERVIEWS;
D O I
10.1016/j.cct.2024.107752
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: As people with cystic fibrosis (PWCF) live longer due to the breakthrough drug elexacaftortezacaftor-ivacaftor (ETI), they have questioned whether other CF therapies could be safely discontinued. SIMPLIFY was the first prospective, randomized trial to evaluate non-inferiority of discontinuing versus continuing two therapies. The QUEST (Qualitative Understanding of Experiences in the SIMPLIFY Trial) study was conducted to understand experiences of PWCF enrolled in SIMPLIFY, including why they joined, perceptions of randomization, decision-making around study withdrawal, and considerations for future discontinuation studies. Methods: QUEST enrolled SIMPLIFY participants 14 years or older stable on ETI and caregivers of the 14-17 year- olds. Interviews were audio-recorded, transcribed, and coded. A phenomenological approach was used to inductively develop codes with no a priori hypotheses; identified themes were then organized around current research and recruitment literature. Results: 114 interviews were completed (68 adults, 23 teenagers, and 23 caregivers). Among PWCF, median age was 27.8 years, 49 % were female and 80 % had participated in research before SIMPLIFY. Five themes were identified: (1) Experience with SIMPLIFY randomization, [2] Trust, [3] Altruism, [4] Perceived personal benefits, and [5]) Perceived risks and protocol burden. Conclusion: QUEST findings highlight how a long-standing culture of research and thoughtful protocol design contributed to SIMPLIFY's successful recruitment and retention. This included understanding the importance of remaining in the trial despite not being randomized to their preferred treatment assignment. Using patient-centered approaches to select research questions, design a protocol to minimize participant barriers, and frame recruitment materials messaging contribute to successful research participation.
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页数:8
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共 29 条
  • [1] [Anonymous], 2017, Cystic Fibrosis Foundation Patient Registry 2016 Annual Data Report
  • [2] cff, 2017, CFF Patient Registry Annual Data Report Internet
  • [3] Motivations for participating in an HIV vaccine efficacy trial
    Colfax, G
    Buchbinder, S
    Vamshidar, G
    Celum, C
    McKirnan, D
    Neidig, J
    Koblin, B
    Gurwith, M
    Bartholow, B
    [J]. JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2005, 39 (03) : 359 - 364
  • [4] Cystic Fibrosis Foundation, 2022, Cystic fibrosis foundation patient registry 2022 annual data report
  • [5] A discrete choice experiment to quantify the influence of trial features on the decision to participate in cystic fibrosis trials
    Dobra, Rebecca
    Davies, Jane
    Elborn, Stuart
    Kee, Frank
    Madge, Susan
    Boeri, Marco
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2024, 23 (01) : 73 - 79
  • [6] A Systematic Review of Barriers and Facilitators to Minority Research Participation Among African Americans, Latinos, Asian Americans, and Pacific Islanders
    George, Sheba
    Duran, Nelida
    Norris, Keith
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2014, 104 (02) : E16 - E31
  • [7] Answering the call to address cystic fibrosis treatment burden in the era of highly effective CFTR modulator therapy
    Gifford, Alex H.
    Mayer-Hamblett, Nicole
    Pearson, Kelsie
    Nichols, David P.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (05) : 762 - 767
  • [8] The cystic fibrosis therapeutics development network (CF TDN): a paradigm of a clinical trials network for genetic and orphan diseases
    Goss, CH
    Mayer-Hamblett, N
    Kronmal, RA
    Ramsey, B
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (11) : 1505 - 1528
  • [9] The cystic fibrosis foundation therapeutics development network: A national effort by the cystic fibrosis foundation to build a clinical trials network
    Goss, Christopher H.
    Mayer-Hamblett, Nicole
    Williams, Judy
    Ramsey, Bonnie W.
    [J]. CHILDRENS HEALTH CARE, 2008, 37 (01) : 5 - 20
  • [10] How many interviews are enough? An experiment with data saturation and variability
    Guest, Greg
    Bunce, Arwen
    Johnson, Laura
    [J]. FIELD METHODS, 2006, 18 (01) : 59 - 82