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Published in: Trials 1/2017

Open Access 01-12-2017 | Research

Framing the conversation: use of PRECIS-2 ratings to advance understanding of pragmatic trial design domains

Authors: Paula Darby Lipman, Kirsty Loudon, Leanora Dluzak, Rachael Moloney, Donna Messner, Catherine M. Stoney

Published in: Trials | Issue 1/2017

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Abstract

Background

There continues to be debate about what constitutes a pragmatic trial and how it is distinguished from more traditional explanatory trials. The NIH Pragmatic Trials Collaborative Project, which includes five trials and a coordinating unit, has adopted the Pragmatic-Explanatory Continuum Indicator Summary (PRECIS-2) instrument. The purpose of the study was to collect PRECIS-2 ratings at two points in time to assess whether the tool was sensitive to change in trial design, and to explore with investigators the rationale for rating shifts.

Methods

A mixed-methods design included sequential collection and analysis of quantitative data (PRECIS-2 ratings) and qualitative data. Ratings were collected at two annual, in-person project meetings, and subsequent interviews conducted with investigators were recorded, transcribed, and coded using NVivo 11 Pro for Windows. Rating shifts were coded as either (1) actual change (reflects a change in procedure or protocol), (2) primarily a rating shift reflecting rater variability, or (3) themes that reflect important concepts about the tool and/or pragmatic trial design.

Results

Based on PRECIS-2 ratings, each trial was highly pragmatic at the planning phase and remained so 1 year later in the early phases of trial implementation. Over half of the 45 paired ratings for the nine PRECIS-2 domains indicated a rating change from Time 1 to Time 2 (N = 24, 53%). Of the 24 rating changes, only three represented a true change in the design of the trial. Analysis of rationales for rating shifts identified critical themes associated with the tool or pragmatic trial design more generally. Each trial contributed one or more relevant comments, with Eligibility, Flexibility of Adherence, and Follow-up each accounting for more than one.

Conclusions

PRECIS-2 has proved useful for “framing the conversation” about trial design among members of the Pragmatic Trials Collaborative Project. Our findings suggest that design elements assessed by the PRECIS-2 tool may represent mostly stable decisions. Overall, there has been a positive response to using PRECIS-2 to guide conversations around trial design, and the project’s focus on the use of the tool by this group of early adopters has provided valuable feedback to inform future trainings on the tool.
Literature
1.
go back to reference Rothwell PM. External validity of randomised controlled trials: “To whom do the results of this trial apply?”. Lancet. 2005;365(9453):82–93. Rothwell PM. External validity of randomised controlled trials: “To whom do the results of this trial apply?”. Lancet. 2005;365(9453):82–93.
2.
go back to reference Treweek S, Zwarenstein M. Making trials matter: pragmatic and explanatory trials and the problem of applicability. Trials. 2009;10(1):37. PMCID: PMC2700087.CrossRefPubMedPubMedCentral Treweek S, Zwarenstein M. Making trials matter: pragmatic and explanatory trials and the problem of applicability. Trials. 2009;10(1):37. PMCID: PMC2700087.CrossRefPubMedPubMedCentral
3.
go back to reference Tunis SR, Stryer DB, Clancy CM. Practical clinical trials: increasing the value of clinical research for decision making in clinical and health policy. JAMA. 2003;290(12):1624–32.CrossRefPubMed Tunis SR, Stryer DB, Clancy CM. Practical clinical trials: increasing the value of clinical research for decision making in clinical and health policy. JAMA. 2003;290(12):1624–32.CrossRefPubMed
4.
go back to reference Schwartz D, Lellouch J. Explanatory and pragmatic attitudes in therapeutical trials. J Clin Epidemiol. 2009;62(5):499–505.CrossRefPubMed Schwartz D, Lellouch J. Explanatory and pragmatic attitudes in therapeutical trials. J Clin Epidemiol. 2009;62(5):499–505.CrossRefPubMed
5.
go back to reference Schwartz D, Lellouch J. Explanatory and pragmatic attitudes in therapeutical trials. J Chronic Dis. 1967;20(8):637–48.CrossRefPubMed Schwartz D, Lellouch J. Explanatory and pragmatic attitudes in therapeutical trials. J Chronic Dis. 1967;20(8):637–48.CrossRefPubMed
6.
go back to reference Saunders C, Byrne CD, Guthrie B, Lindsay RS, McKnight JA, Philip S, Sattar N, Walker JJ, Wild SH. External validity of randomized controlled trials of glycaemic control and vascular disease: how representative are participants? Diabet Med. 2013;30(3):300–8.CrossRefPubMed Saunders C, Byrne CD, Guthrie B, Lindsay RS, McKnight JA, Philip S, Sattar N, Walker JJ, Wild SH. External validity of randomized controlled trials of glycaemic control and vascular disease: how representative are participants? Diabet Med. 2013;30(3):300–8.CrossRefPubMed
7.
go back to reference Kennedy-Martin T, Curtis S, Faries D, Robinson S, Johnston J. A literature review on the representativeness of randomized controlled trial samples and implications for the external validity of trial results. Trials. 2015;16:495. PMCID: PMC4632358.CrossRefPubMedPubMedCentral Kennedy-Martin T, Curtis S, Faries D, Robinson S, Johnston J. A literature review on the representativeness of randomized controlled trial samples and implications for the external validity of trial results. Trials. 2015;16:495. PMCID: PMC4632358.CrossRefPubMedPubMedCentral
9.
go back to reference Loudon K, Treweek S, Sullivan F, Donnan P, Thorpe KE, Zwarenstein M. The PRECIS-2 tool: designing trials that are fit for purpose. BMJ. 2015;350:h2147.CrossRefPubMed Loudon K, Treweek S, Sullivan F, Donnan P, Thorpe KE, Zwarenstein M. The PRECIS-2 tool: designing trials that are fit for purpose. BMJ. 2015;350:h2147.CrossRefPubMed
10.
go back to reference Moher D, Glasziou P, Chalmers I, Nasser M, Bossuyt PM, Korevaar DA, Graham ID, Ravaud P, Boutron I. Increasing value and reducing waste in biomedical research: who’s listening? Lancet. 2016;387(10027):1573–86.CrossRefPubMed Moher D, Glasziou P, Chalmers I, Nasser M, Bossuyt PM, Korevaar DA, Graham ID, Ravaud P, Boutron I. Increasing value and reducing waste in biomedical research: who’s listening? Lancet. 2016;387(10027):1573–86.CrossRefPubMed
11.
go back to reference Johnson KE, Neta G, Dember LM, Coronado GD, Suls J, Chambers DA, Rundell S, Smith DH, Liu B, Taplin S, Stoney CM. Use of PRECIS ratings in the National Institutes of Health (NIH) Health Care Systems Research Collaboratory. Trials. 2016;17(1):32.CrossRefPubMedPubMedCentral Johnson KE, Neta G, Dember LM, Coronado GD, Suls J, Chambers DA, Rundell S, Smith DH, Liu B, Taplin S, Stoney CM. Use of PRECIS ratings in the National Institutes of Health (NIH) Health Care Systems Research Collaboratory. Trials. 2016;17(1):32.CrossRefPubMedPubMedCentral
13.
go back to reference Riddle DL, Johnson RE, Jensen MP, Keefe FJ, Kroenke K, Bair MJ, Ang DC. The Pragmatic-Explanatory Continuum Indicator Summary (PRECIS) instrument was useful for refining a randomized trial design: experiences from an investigative team. J Clin Epidemiol. 2010;63(11):1271–5.CrossRefPubMedPubMedCentral Riddle DL, Johnson RE, Jensen MP, Keefe FJ, Kroenke K, Bair MJ, Ang DC. The Pragmatic-Explanatory Continuum Indicator Summary (PRECIS) instrument was useful for refining a randomized trial design: experiences from an investigative team. J Clin Epidemiol. 2010;63(11):1271–5.CrossRefPubMedPubMedCentral
14.
go back to reference Thorpe KE, Zwarenstein M, Oxman AD, Treweek S, Furberg CD, Altman DG, Tunis S, Bergel E, Harvey I, Magid DJ, Chalkidou K. A pragmatic-explanatory continuum indicator summary (PRECIS): a tool to help trial designers. J Clin Epidemiol. 2009;62(5):464–75.CrossRefPubMed Thorpe KE, Zwarenstein M, Oxman AD, Treweek S, Furberg CD, Altman DG, Tunis S, Bergel E, Harvey I, Magid DJ, Chalkidou K. A pragmatic-explanatory continuum indicator summary (PRECIS): a tool to help trial designers. J Clin Epidemiol. 2009;62(5):464–75.CrossRefPubMed
15.
go back to reference Zwarenstein M, Treweek S, Loudon K. PRECIS-2 helps researchers design more applicable RCTs while CONSORT Extension for Pragmatic Trials helps knowledge users decide whether to apply them. J Clinical Epidemiol. 2017;84:27–9.CrossRef Zwarenstein M, Treweek S, Loudon K. PRECIS-2 helps researchers design more applicable RCTs while CONSORT Extension for Pragmatic Trials helps knowledge users decide whether to apply them. J Clinical Epidemiol. 2017;84:27–9.CrossRef
18.
go back to reference Zuidgeest MG. Goetz I, Grobbee DE, WP3 of the GetReal Consortium. PRECIS-2 in perspective: what is next for pragmatic trials? J Clin Epidemiol. 2017;84:22–4.CrossRefPubMed Zuidgeest MG. Goetz I, Grobbee DE, WP3 of the GetReal Consortium. PRECIS-2 in perspective: what is next for pragmatic trials? J Clin Epidemiol. 2017;84:22–4.CrossRefPubMed
19.
go back to reference Gupta A, Thorpe C, Zwarenstein M. Why most randomized controlled trials are irrelevant. Can Fam Physician. 2015;61(9):811–2. PMCID: PMC4569116. Epub 2015/09/16. eng.PubMedPubMedCentral Gupta A, Thorpe C, Zwarenstein M. Why most randomized controlled trials are irrelevant. Can Fam Physician. 2015;61(9):811–2. PMCID: PMC4569116. Epub 2015/09/16. eng.PubMedPubMedCentral
20.
go back to reference Witkiewitz K, Finney JW, Harris AH, Kivlahan DR, Kranzler HR. Recommendations for the design and analysis of treatment trials for alcohol use disorders. Alcohol Clin Exp Res. 2015;39(9):1557–70. PMCID: PMC4558228. Epub 2015/08/08. eng.CrossRefPubMedPubMedCentral Witkiewitz K, Finney JW, Harris AH, Kivlahan DR, Kranzler HR. Recommendations for the design and analysis of treatment trials for alcohol use disorders. Alcohol Clin Exp Res. 2015;39(9):1557–70. PMCID: PMC4558228. Epub 2015/08/08. eng.CrossRefPubMedPubMedCentral
21.
go back to reference Riddle DL. Consequences of randomized clinical trial design decisions need to be clarified. J Clin Epidemiol. 2016;77:13.CrossRefPubMed Riddle DL. Consequences of randomized clinical trial design decisions need to be clarified. J Clin Epidemiol. 2016;77:13.CrossRefPubMed
22.
go back to reference Randolph AG. Pragmatic trials in critically ill children are CATCHing on. Lancet. 2016;387(10029):1697.CrossRefPubMed Randolph AG. Pragmatic trials in critically ill children are CATCHing on. Lancet. 2016;387(10029):1697.CrossRefPubMed
23.
go back to reference Dekkers OM, Bossuyt PM, Vandenbroucke JP. How trial results are intended to be used: is PRECIS-2 a step forward? J Clin Epidemiol. 2017;84:25–6.CrossRefPubMed Dekkers OM, Bossuyt PM, Vandenbroucke JP. How trial results are intended to be used: is PRECIS-2 a step forward? J Clin Epidemiol. 2017;84:25–6.CrossRefPubMed
24.
go back to reference English M, Irimu G, Agweyu A, Gathara D, Oliwa J, Ayieko P, Were F, Paton C, Tunis S, Forrest CB. Building Learning Health Systems to accelerate research and improve outcomes of clinical care in low-and middle-income countries. PLoS Med. 2016;13(4):e1001991. PMCID: PMC4829240.CrossRefPubMedPubMedCentral English M, Irimu G, Agweyu A, Gathara D, Oliwa J, Ayieko P, Were F, Paton C, Tunis S, Forrest CB. Building Learning Health Systems to accelerate research and improve outcomes of clinical care in low-and middle-income countries. PLoS Med. 2016;13(4):e1001991. PMCID: PMC4829240.CrossRefPubMedPubMedCentral
25.
go back to reference Gaglio B, Phillips SM, Heurtin-Roberts S, Sanchez MA, Glasgow RE. How pragmatic is it? Lessons learned using PRECIS and RE-AIM for determining pragmatic characteristics of research. Implement Sci. 2014;9(1):96.CrossRefPubMedPubMedCentral Gaglio B, Phillips SM, Heurtin-Roberts S, Sanchez MA, Glasgow RE. How pragmatic is it? Lessons learned using PRECIS and RE-AIM for determining pragmatic characteristics of research. Implement Sci. 2014;9(1):96.CrossRefPubMedPubMedCentral
26.
go back to reference Jarvik JG, Comstock BA, James KT, Avins AL, Bresnahan BW, Deyo RA, Luetmer PH, Friedly JL, Meier EN, Cherkin DC, Gold LS. Lumbar Imaging with Reporting of Epidemiology (LIRE)—protocol for a pragmatic cluster randomized trial. Contemp Clin Trials. 2015;45:157–63. PMCID: PMC4674321.CrossRefPubMedPubMedCentral Jarvik JG, Comstock BA, James KT, Avins AL, Bresnahan BW, Deyo RA, Luetmer PH, Friedly JL, Meier EN, Cherkin DC, Gold LS. Lumbar Imaging with Reporting of Epidemiology (LIRE)—protocol for a pragmatic cluster randomized trial. Contemp Clin Trials. 2015;45:157–63. PMCID: PMC4674321.CrossRefPubMedPubMedCentral
27.
go back to reference Santer M, Rumsby K, Ridd MJ, Francis NA, Stuart B, Chorozoglou M, Wood W, Roberts A, Thomas KS, Williams HC, Little P. Bath additives for the treatment of childhood eczema (BATHE): protocol for multicentre parallel group randomised trial. BMJ Open. 2015;5(10):e009575. PMCID: PMC4636671.CrossRefPubMedPubMedCentral Santer M, Rumsby K, Ridd MJ, Francis NA, Stuart B, Chorozoglou M, Wood W, Roberts A, Thomas KS, Williams HC, Little P. Bath additives for the treatment of childhood eczema (BATHE): protocol for multicentre parallel group randomised trial. BMJ Open. 2015;5(10):e009575. PMCID: PMC4636671.CrossRefPubMedPubMedCentral
28.
go back to reference Creswell JW, Klassen AC, Plano Clark VL, Smith KC. Best practices for mixed methods research in the health sciences. Bethesda (Maryland): National Institutes of Health; 2011. p. 2094–103. Creswell JW, Klassen AC, Plano Clark VL, Smith KC. Best practices for mixed methods research in the health sciences. Bethesda (Maryland): National Institutes of Health; 2011. p. 2094–103.
29.
go back to reference Creswell JW. Research design: qualitative, quantitative, and mixed methods approaches. Thousand Oaks: Sage publications; 2013. Creswell JW. Research design: qualitative, quantitative, and mixed methods approaches. Thousand Oaks: Sage publications; 2013.
30.
go back to reference Wildes TS, Winter AC, Maybrier HR, Mickle AM, Lenze EJ, Stark S, Lin N, Inouye SK, Schmitt EM, McKinnon SL, Muench MR. Protocol for the Electroencephalography Guidance of Anesthesia to Alleviate Geriatric Syndromes (ENGAGES) study: a pragmatic, randomised clinical trial. BMJ Open. 2016;6(6):e011505. doi:10.1136/bmjopen-2016-011505. Wildes TS, Winter AC, Maybrier HR, Mickle AM, Lenze EJ, Stark S, Lin N, Inouye SK, Schmitt EM, McKinnon SL, Muench MR. Protocol for the Electroencephalography Guidance of Anesthesia to Alleviate Geriatric Syndromes (ENGAGES) study: a pragmatic, randomised clinical trial. BMJ Open. 2016;6(6):e011505. doi:10.​1136/​bmjopen-2016-011505.
31.
go back to reference Levenson JC, Rollman BL, Ritterband LM, Strollo PJ, Smith KJ, Yabes JG, Moore CG, Harvey AG, Buysse DJ. Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial. Trials. 2017;18(1):256.CrossRefPubMedPubMedCentral Levenson JC, Rollman BL, Ritterband LM, Strollo PJ, Smith KJ, Yabes JG, Moore CG, Harvey AG, Buysse DJ. Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial. Trials. 2017;18(1):256.CrossRefPubMedPubMedCentral
32.
go back to reference Wang HE, Prince DK, Stephens SW, Herren H, Daya M, Richmond N, Carlson J, Warden C, Colella MR, Brienza A, Aufderheide TP. Design and implementation of the resuscitation outcomes consortium pragmatic airway resuscitation trial (PART). Resuscitation. 2016;101:57–64.CrossRefPubMedPubMedCentral Wang HE, Prince DK, Stephens SW, Herren H, Daya M, Richmond N, Carlson J, Warden C, Colella MR, Brienza A, Aufderheide TP. Design and implementation of the resuscitation outcomes consortium pragmatic airway resuscitation trial (PART). Resuscitation. 2016;101:57–64.CrossRefPubMedPubMedCentral
33.
go back to reference Gong MN, Schenk L, Gajic O, Mirhaji P, Sloan J, Dong Y, Festic E, Herasevich V. Early intervention of patients at risk for acute respiratory failure and prolonged mechanical ventilation with a checklist aimed at the prevention of organ failure: protocol for a pragmatic stepped-wedged cluster trial of PROOFCheck. BMJ Open. 2016;6, e011347. doi:10.1136/bmjopen-2016-011347.CrossRefPubMedPubMedCentral Gong MN, Schenk L, Gajic O, Mirhaji P, Sloan J, Dong Y, Festic E, Herasevich V. Early intervention of patients at risk for acute respiratory failure and prolonged mechanical ventilation with a checklist aimed at the prevention of organ failure: protocol for a pragmatic stepped-wedged cluster trial of PROOFCheck. BMJ Open. 2016;6, e011347. doi:10.​1136/​bmjopen-2016-011347.CrossRefPubMedPubMedCentral
34.
go back to reference Courtright KR, Madden V, Gabler NB, Cooney E, Small DS, Troxel A, Casarett D, Ersek M, Cassel JB, Nicholas LH, Escobar G. Rationale and design of the Randomized Evaluation of Default Access to Palliative Services (REDAPS) Trial. Ann Am Thorac Soc. 2016;13(9):1629–39. doi:10.1513/AnnalsATS.201604-308OT. Courtright KR, Madden V, Gabler NB, Cooney E, Small DS, Troxel A, Casarett D, Ersek M, Cassel JB, Nicholas LH, Escobar G. Rationale and design of the Randomized Evaluation of Default Access to Palliative Services (REDAPS) Trial. Ann Am Thorac Soc. 2016;13(9):1629–39. doi:10.​1513/​AnnalsATS.​201604-308OT.
Metadata
Title
Framing the conversation: use of PRECIS-2 ratings to advance understanding of pragmatic trial design domains
Authors
Paula Darby Lipman
Kirsty Loudon
Leanora Dluzak
Rachael Moloney
Donna Messner
Catherine M. Stoney
Publication date
01-12-2017
Publisher
BioMed Central
Published in
Trials / Issue 1/2017
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-017-2267-y

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