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Preregistration (science)

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principle acceptance). The proposed study is then performed, and the research report is submitted for Stage 2 peer review. Stage 2 peer review confirms that the actual research methods are consistent with the preregistered protocol, that quality thresholds are met (e.g., manipulation checks confirm the validity of the experimental manipulation), and that the conclusions follow from the data. Because studies are accepted for publication regardless of whether the results are statistically significant Registered Reports prevent publication bias. Meta-scientific research has shown that the percentage of non-significant results in Registered Reports is substantially higher than in standard publications.
90:. The preregistered study is then conducted, and a report of the study and its results is submitted for publication together with access to the preregistration document. This preregistration approach allows peer reviewers and subsequent readers to cross-reference the preregistration document with the published research article in order to identify the presence of any undisclosed deviations of the preregistration. Deviations from the preregistration are possible and common in practice, but they should be transparently reported, and the consequences for the severity of the test should be evaluated. 211:(NLM) was the first online registry for clinical trials, and remains the largest and most widely used. In addition to combating bias, clinical trial registries serve to increase transparency and access to clinical trials for the public. Clinical trials registries are often searchable (e.g. by disease/indication, drug, location, etc.). Trials are registered by the pharmaceutical, biotech or medical device company (Sponsor) or by the hospital or foundation which is sponsoring the study, or by another organization, such as a 232:
international and written about for over 50 years. One of the proposals to address this potential bias was a comprehensive register of initiated clinical trials that would inform the public which trials had been started. Ethical issues were those that seemed to interest the public most, as trialists (including those with potential commercial gain) benefited from those who enrolled in trials, but were not required to “give back,” telling the public what they had learned.
3990: 731:). The most frequent deviations were with regards to the planned sample size, exclusion criteria, and statistical model. Hence, what were intended as preregistered confirmatory tests ended up as unplanned exploratory tests. Again, preregistration advocates argue that deviations from preregistered plans are acceptable as long as they are reported transparently and justified. They also point out that even vague preregistrations help to reduce 413:
biomedical research relies on animal experiments. The non-publication of results gained from animal experiments not only distorts the state of research by reinforcing the publication bias, it further represents an ethical issue. Preregistration is discussed as a measure that could counteract this problem. Following registries are suited for the preregistration of preclinical studies.
723:). For example, pre-registered studies are only of higher quality than non-pre registered studies in that the former does has a power analysis and higher sample size than the latter but other than that they do not seem to prevent p-hacking and HARKing, as both the proportion of positive results and effect sizes are similar between preregistered and non-preregistered studies ( 592:). In response, preregistration advocates have stressed that exploratory analyses are permitted in preregistered studies, and that the results of these analyses retain some value vis-a-vis hypothesis generation rather than hypothesis testing. Preregistration merely makes the distinction between confirmatory and exploratory research clearer ( 612:). However, critics counterargue that, if preregistration is only supposed to be a plan, and not a prison, then researchers should feel free to deviate from that plan and undertake exploratory analyses without fearing accusations of low research credibility due to circular reasoning and inappropriate research practices such as 539:
concepts and students felt that they understood their dissertation and it improved the clarity of the manuscript writing, promoted rigour and were more likely to avoid questionable research practices. In addition, it becomes a tool that can supervisors can use to shape students to combat any questionable research practices.
264:(ICMJE) announced that their journals would not publish reports of trials unless they had been registered. The ICMJE action was probably the most important motivator for trial registration, as investigators wanted to reserve the possibility that they could publish their results in prestigious journals, should they want to. 584:). Circular reasoning can be identified by analysing the reasoning per se without needing to know whether that reasoning was preregistered. Critics have also noted that the idea that preregistration improves research credibility may deter researchers from undertaking non-preregistered exploratory analyses ( 535:). The primary goal of preregistration is to improve the transparency of reported hypothesis tests, which allows readers to evaluate the extent to which decisions during the data analysis were pre-planned (maintaining statistical error control) or data-driven (increasing the Type 1 or Type 2 error rate). 538:
Meta-scientific research has revealed additional benefits. Researchers indicate preregistering a study leads to a more carefully thought through research hypothesis, experimental design, and statistical analysis. In addition, preregistration has been shown to encourage better learning of Open Science
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Those who were particularly concerned by the double standard were systematic reviewers, those who summarize what is known from clinical trials. If the literature is skewed, then the results of a systematic review are also likely to be skewed, possibly favoring the test intervention when in fact the
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For many years, scientists and others have worried about reporting biases such that negative or null results from initiated clinical trials may be less likely to be published than positive results, thus skewing the literature and our understanding of how well interventions work. This worry has been
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In the standard preregistration format, researchers prepare a research protocol document prior to conducting their research. Ideally, this document indicates the research hypotheses, sampling procedure, sample size, research design, testing conditions, stimuli, measures, data coding and aggregation
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defines this format: “In a registered report, authors create a study proposal that includes theoretical and empirical background, research questions/hypotheses, and pilot data (if available). Upon submission, this proposal will then be reviewed prior to data collection, and if accepted, the paper
305:. WHO states that the international registry's mission is "to ensure that a complete view of research is accessible to all those involved in health care decision making. This will improve research transparency and will ultimately strengthen the validity and value of the scientific evidence base." 755:
changes that have led up to the current method and analyses” (pp. 378–379). In addition, pre-registering a study requires careful deliberation about the study's hypotheses, research design and statistical analyses. This depends on the use of pre-registration templates that provides detailed
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The registered report format requires authors to submit a description of the study methods and analyses prior to data collection. Once the theoretical introduction, method, and analysis plan has been peer reviewed (Stage 1 peer review), publication of the findings is provisionally guaranteed (in
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Similar to clinical research, preregistration can help to improve transparency and quality of research data in preclinical research. In contrast to clinical research where preregistration is mandatory for vast parts it is still new in preclinical research. A large part of preclinical and basic
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Note that only a very small proportion of academic journals in psychology and neurosciences explicitly stated that they welcome submissions of replication studies in their aim and scope or instructions to authors. This phenomenon does not encourage the reporting or even attempt on replication
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Pownall, Madeleine; Pennington, Charlotte R.; Norris, Emma; Juanchich, Marie; Smailes, David; Russell, Sophie; Gooch, Debbie; Evans, Thomas Rhys; Persson, Sofia; Mak, Matthew H. C.; Tzavella, Loukia; Monk, Rebecca; Gough, Thomas; Benwell, Christopher S. Y.; Elsherif, Mahmoud (October 2023).
246:(Food and Drug Administration Modernization Act of 1997. Pub L No. 105-115, §113 Stat 2296), but the law provided neither funding nor a mechanism of enforcement. In addition, the law required that ClinicalTrials.gov only include trials of serious and life-threatening diseases. 3424: 609: 795:
for inconclusive evidence), although it is unclear whether this represents a "false" sense of credibility due to pre-existing positive community attitudes about preregistration or a genuine causal effect of registered reports on quality of research.
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Akker, Olmo R. van den; Weston, Sara; Campbell, Lorne; Chopik, Bill; Damian, Rodica; Davis-Kean, Pamela; Hall, Andrew; Kosie, Jessica; Kruse, Elliott; Olsen, Jerome; Ritchie, Stuart; Valentine, K. D.; Veer, Anna van 't; Bakker, Marjan (2021-11-09).
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Toth, Allison A.; Banks, George C.; Mellor, David; O’Boyle, Ernest H.; Dickson, Ashleigh; Davis, Daniel J.; DeHaven, Alex; Bochantin, Jaime; Borns, Jared (1 August 2021). "Study Preregistration: An Evaluation of a Method for Transparent Reporting".
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International Collaborative Group on Clinical Trial Registries (1993). "Position paper and consensus recommendations on clinical trial registries. Ad Hoc Working Party of the International Collaborative Group on Clinical Trials Registries".
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ICMJE accepts all primary registries in the WHO network in addition to clinicaltrials.gov. Clinical trial registration in other registries excluding ClinicalTrials.gov has increased irrespective of study designs since 2014.
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There has been a push from governments and international organizations, especially since 2005, to make clinical trial information more widely available and to standardize registries and processes of registering. The
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Parsons, Sam; Azevedo, Flávio; Elsherif, Mahmoud M.; Guay, Samuel; Shahim, Owen N.; Govaart, Gisela H.; Norris, Emma; O’Mahony, Aoife; Parker, Adam J.; Todorovic, Ana; Pennington, Charlotte R. (2022-02-21).
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method, criteria for data exclusions, and statistical analyses, including potential variations on those analyses. This preregistration document is then posted on a publicly available website such as the
200:. Registration of clinical trials is required in some countries and is increasingly being standardized. Some top medical journals will only publish the results of trials that have been pre-registered. 64:
increase the probability of incorrect claims. Although the idea is old, the practice of preregistering studies has gained prominence to mitigate to some of the issues that are thought to underlie the
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Akker, Olmo R. van den; Weston, Sara; Campbell, Lorne; Chopik, Bill; Damian, Rodica; Davis-Kean, Pamela; Hall, Andrew; Kosie, Jessica; Kruse, Elliott; Olsen, Jerome; Ritchie, Stuart (2021-11-09).
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also noted that the editorial staff will be asking for replication of studies with surprising findings from examinations using small sample sizes before allowing the manuscripts to be published.
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Singh, B.; Fairman, C. M.; Christensen, J. F.; Bolam, K. A.; Twomey, R.; Nunan, D.; Lahart, I. M. (2021). "Outcome reporting bias in exercise oncology trials (OREO): A cross-sectional study".
294:. There has also been action from the pharmaceutical industry, which released plans to make clinical trial data more transparent and publicly available. Released in October 2008, the revised 771:
Finally, some commentators have argued that, under some circumstances, preregistration may actually harm science by providing a false sense of credibility to research studies and analyses (
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preregistration in economics journals found that preregistration did not reduce p-hacking and publication bias, unless the preregistration was accompanied by a preanalysis plan.
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Scheel, Anne M.; Schijen, Mitchell R. M. J.; Lakens, Daniël (April 2021). "An Excess of Positive Results: Comparing the Standard Psychology Literature With Registered Reports".
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Banno, M; Tsujimoto, Y; Kataoka, Y (2019). "Studies registered in non-ClinicalTrials.gov accounted for an increasing proportion of protocol registrations in medical research".
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has adopted the registered report format, as it “shift the emphasis from the results of research to the questions that guide the research and the methods used to answer them”.
268: 271:(FDAAA) clarified the requirements for registration and also set penalties for non-compliance (Public Law 110-85. The Food and Drug Administration Amendments Act of 2007 261: 2550:"Publication rates in animal research. Extent and characteristics of published and non-published animal studies followed up at two German university medical centres" 787:). Consistent with this view, there is some evidence that researchers view registered reports as being more credible than standard reports on a range of dimensions ( 291: 1669:
Bert, Bettina; Heinl, Céline; Chmielewska, Justyna; Schwarz, Franziska; Grune, Barbara; Hensel, Andreas; Greiner, Matthias; Schönfelder, Gilbert (2019-10-15).
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Preregistration has the goal to allow others to transparently evaluate the capacity of a test to falsify a prediction. A number of research practices such as
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Bakker, M.; Veldkamp, C. L. S.; van Assen, M. A. L. M.; Crompvoets, E. A. V.; Ong, H. H.; Nosek, B.; Soderberg, C. K.; Mellor, D.; Wicherts, J. M. (2020).
2317:"Clinical trial registration, reporting, publication and FDAAA compliance: a cross-sectional analysis and ranking of new drugs approved by the FDA in 2012" 544: 648:). Finally, and more fundamentally, critics have argued that the distinction between confirmatory and exploratory analyses is unclear and/or irrelevant ( 208: 3274:"Do Preregistration and Preanalysis Plans Reduce p -Hacking and Publication Bias? Evidence from 15,992 Test Statistics and Suggestions for Improvement" 249:
Then, two events occurred in 2004 that increased public awareness of the problems of reporting bias. First, the then-New York State Attorney General
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Bowman, Sara D.; Dehaven, Alexander Carl; Errington, Timothy M.; Hardwicke, Tom Elis; Mellor, David Thomas; Nosek, Brian A.; Soderberg, Courtney K.
739:). However, critics have argued that it is not useful to identify or justify deviations from preregistered plans when those plans do not reflect 768:). Many pre-registration template stress the importance of a power analysis but not only stress the importance of why the methodology was used. 335:
Worldwide, there is growing number of registries. A 2013 study identified the following top five registries (numbers updated as of August 2013):
286:(ICMJE) decided that from July 1, 2005 no trials will be considered for publication unless they are included on a clinical trials registry. The 580:, p. 2600). However, critics have argued that preregistration is not necessary to identify circular reasoning during exploratory analyses ( 3189: 4503:
Soderberg, C. K.; Errington, T. M.; Schiavone, S R.; Bottesini, J.; Singleton Thorn, F.; Vazire, S.; Esterling, K. M.; Nosek, B. A. (2020).
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van den Akker, Olmo R.; van Assen, Marcel A. L. M.; Bakker, Marjan; Elsherif, Mahmoud; Wong, Tsz Keung; Wicherts, Jelte M. (2023-11-10).
2385:"Evaluating adherence to the International Committee of Medical Journal Editors' policy of mandatory, timely clinical trial registration" 1877:
Sterling, TD (1959). "Publication decisions and their possible effects on inferences drawn from tests of significances – or vice versa".
3207:"Questionable research practices in student final theses – Prevalence, attitudes, and the role of the supervisor's perceived attitudes" 2365: 1583:"Making the black box transparent: A template and tutorial for (pre-)registration of studies using experience sampling methods (ESM)" 727:). In addition, in a survey of 27 preregistered studies found that researchers deviated from their preregistered plans in all cases ( 675:
There are also concerns about the practical implementation of preregistration. Many preregistered protocols leave plenty of room for
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Various studies have measured the extent to which various trials are in compliance with the reporting standards of their registry.
298:, states that "Every clinical trial must be registered in a publicly accessible database before recruitment of the first subject." 2548:
Wieschowski, Susanne; Biernot, Svenja; Deutsch, Susanne; Glage, Silke; Bleich, André; Tolba, René; Strech, Daniel (2019-11-26).
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Nosek, Brian A.; Lakens, Daniël (1 May 2014). "Registered Reports: A Method to Increase the Credibility of Published Results".
499: 479: 4190:"Pre-registration is a game changer. But, like random assignment, it is neither necessary nor sufficient for credible science" 3924:"Preregistration specificity & adherence: A review of preregistered gambling studies & cross-disciplinary comparison" 2434:"Animal Study Registries: Results from a Stakeholder Analysis on Potential Strengths, Weaknesses, Facilitators, and Barriers" 212: 2170:
Anderson, Monique L.; Chiswell, Karen; Peterson, Eric D.; Tasneem, Asba; Topping, James; Califf, Robert M. (12 March 2015).
628:). Again, they have pointed out that preregistration is not necessary to address such concerns. For example, concerns about 1940:
Dickersin, K; Rennie, D (2012). "The evolution of trial registries and their use to assess the clinical trial enterprise".
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Sun, L. W.; Lee, D. J.; Collins, J. A.; Carll, T. C.; Ramahi, K.; Sandy, S. J.; Unteriner, J. G.; Weinberg, D. V. (2019).
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was originally developed largely as a result of breast cancer consumer lobbying, which led to authorizing language in the
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is working toward "achieving consensus on both the minimal and the optimal operating standards for trial registration".
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Naald, Mira van der; Wenker, Steven; Doevendans, Pieter A.; Wever, Kimberley E.; Chamuleau, Steven A. J. (2020-08-01).
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analyses because they may involve "circular reasoning" in which post hoc hypotheses are based on the observed data (
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Bosnjak, M.; Fiebach, C. J.; Mellor, D.; Mueller, S.; O’Connor, D. B.; Oswald, F. L.; Sokol-Chang, R. I. (2021). .
257:(GSK) because they had failed to reveal results from trials showing that certain antidepressants might be harmful. 556:
Proponents of preregistration have argued that it is "a method to increase the credibility of published results" (
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is the practice of registering the hypotheses, methods, or analyses of a scientific study before it is conducted.
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has encouraged the preregistration of studies and the reporting of effect sizes and confidence intervals. The
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Preregistration can be used in relation to a variety of different research designs and methods, including:
2221:"Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study" 621: 491: 83: 3725:
Szollosi, A.; Kellen, D.; Navarro, D. J.; Shiffrin, R.; van Rooji, I.; Van Zandt, T.; Donkin, C. (2020).
2220: 4598: 4528: 4384: 3953:"Preregistration in practice: A comparison of preregistered and non-preregistered studies in psychology" 3695: 3474: 1270: 1005:
Lakens, Daniël (2019). "The value of preregistration for psychological science: A conceptual analysis".
471:), and the number of journals that are adopting registered reports is approximately doubling each year ( 424: 4446:"The effect of preregistration on trust in empirical research findings: Results of a registered report" 4444:
Field, S. M.; Wagenmakers, E. J.; Kiers, H. A.; Hoekstra, R.; Ernst, A.F.; van Ravenzwaaij, D. (2020).
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Heirene, R.; LaPlante, D.; Louderback, E. R.; Keen, B.; Bakker, M.; Serafimovska, A.; Gainsbury, S. M.
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Sarafoglou, Alexandra; Kovacs, Marton; Bakos, Bence; Wagenmakers, Eric-Jan; Aczel, Balazs (July 2022).
3680:"Arrested theory development: The misguided distinction between exploratory and confirmatory research" 4593: 4583: 4457: 3899: 3218: 3143:"Evaluating the Pedagogical Effectiveness of Study Preregistration in the Undergraduate Dissertation" 3096: 2561: 864: 761: 119: 4009: 2674:"Registered Reports: Peer review before results are known to align scientific values and practices" 680: 169: 162: 2064:"WHO facilitates international collaboration in setting standards for clinical trial registration" 636:
practices, such as (a) open data and research materials and (b) robustness or multiverse analyses
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resulting from this peer-reviewed procedure will be published, regardless of the study outcomes.”
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include the peer review and in principle acceptance of a study protocol prior to data collection.
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is similar, although it may not require the registration of a study's analysis protocol. Finally,
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Wagenmakers, E. J.; Wetzels, R.; Borsboom, D.; van der Maas, H. L.; Kievit, R. A. (2012).
1283: 484: 254: 197: 744: 661: 653: 637: 632:-hacking and unreported multiple testing can be addressed if researchers engage in other 593: 581: 577: 565: 528: 4461: 3993: This article incorporates text from this source, which is available under the 3222: 3100: 2689:"Science in flux: Registered Reports and beyond at the European Journal of Neuroscience" 2565: 868: 17: 4480: 4445: 4165: 4138: 4065: 4038: 3849: 3822: 3273: 3249: 3206: 3117: 3084: 2935: 2900: 2876: 2841: 2649: 2592: 2549: 2525: 2492: 2468: 2433: 2409: 2384: 2341: 2316: 2292: 2267: 2196: 2171: 1705: 1670: 1646: 1619: 1581:
Kirtley, O. J.; Lafit, G.; Achterhof, R.; Hiekkaranta, A. P.; Myin-Germeys, I. (2019).
1425: 1398: 1366: 1339: 1210: 1183: 887: 852: 515:, which maintains a list of journals encouraging the submission of registered reports. 185: 2236: 2079: 1820: 1399:"Recommendations for increasing the transparency of analysis of preexisting data sets" 560:), that it "makes your science better by increasing the credibility of your results" ( 4577: 4520: 4376: 4248: 4213: 4155: 4082: 3807: 3758: 3664: 3545: 3466: 3409: 2252: 2156: 1604: 1558: 1516: 1383: 1262: 970: 920: 776: 765: 757: 728: 704: 657: 625: 564:), and that it "improves the interpretability and credibility of research findings" ( 250: 155: 134: 112: 53: 3621: 3370: 3345:"Pre-analysis plans have limited upside, especially where replications are feasible" 3182:
A student's guide to open science: using the replication crisis to reform psychology
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A clinical trials registry is a platform which catalogs registered clinical trials.
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during the data analysis stage, it is also supposed to be “a plan, not a prison” (
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Overall, the number of participating journals is increasing, as indicated by the
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Lakens, Daniël (14 May 2024). "When and How to Deviate From a Preregistration".
815: 3965: 3952: 3799: 3742: 3312:"Registered reports: A method to increase the credibility of published results" 3069: 3031:"The value of preregistration for psychological science: A conceptual analysis" 1758:"WHO | Working Group on Best Practice for Clinical Trials Registers (BPG)" 936: 712: 3655: 3385: 3272:
Brodeur, Abel; Cook, Nikolai M.; Hartley, Jonathan S.; Heyes, Anthony (2024).
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has begun the push for clinical trial registration with the initiation of the
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Claesen, A.; Gomes, S.; Tuerlinckx, F.; Vanpaemel, W.; Leuven, K. U. (2019).
3974: 3773: 3726: 3577: 3560: 3293: 3240: 3166: 2999: 2926: 2917: 2901:"Are Psychology Journals Anti-replication? A Snapshot of Editorial Practices" 2867: 2858: 2763: 2754: 2737: 2640: 2583: 2516: 2459: 1696: 1507: 1490: 1475: 1415: 954: 780: 736: 472: 4512: 4368: 4240: 4055: 3687: 3613: 3536: 3509: 3458: 2803: 2786: 1765: 1595: 1582: 1548: 1531: 1246: 1080: 877: 805: 301:
The World Health Organization maintains an international registry portal at
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Bakan, David (1966). "The test of significance in psychological research".
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Guidelines for creating registered reports by the Center for Open Science
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Several articles have outlined the rationale for preregistration (e.g.,
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Devezer, B.; Navarro, D. J.; Vandekerckhove, J.; Buzbas, E. O. (2020).
1898: 1184:"Open science challenges, benefits and tips in early career and beyond" 572:
analyses are less "credible" and/or "interpretable" than preregistered
126: 61: 4429: 4413:"Preregistration is neither sufficient nor necessary for good science" 4412: 4205: 3679: 3450: 2842:"Do Neuroscience Journals Accept Replications? A Survey of Literature" 2827:"Streamlined review and registered reports soon to be official at EJP" 2705: 2688: 2617:"Publication rate in preclinical research: a plea for preregistration" 1995:"ICMJE: Frequently Asked Questions about Clinical Trials Registration" 1532:"Making ERP research more transparent: Guidelines for preregistration" 945: 4320:"Preregistration of secondary data analysis: A template and tutorial" 2508: 1450:"Preregistration of secondary data analysis: A template and tutorial" 1045: 851:
Nosek, B. A.; Ebersole, C. R.; DeHaven, A. C.; Mellor, D. T. (2018).
4189: 3602:"Sound inference in complicated research: A multi-strategy approach" 3510:"Does preregistration improve the credibility of research findings?" 2432:
Wieschowski, Susanne; Silva, Diego S.; Strech, Daniel (2016-11-10).
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Miller, Jennifer E; Korn, David; Ross, Joseph S (12 November 2015).
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Boghdadly, K. El.; Wiles, M. D.; Atton, S.; Bailey, C. R. (2018).
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explained, “we should be more interested in the rationale for the
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accumulated data do not show this, if all data were made public.
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Steegen, S.; Tuerlinckx, F.; Gelman, A.; Vanpaemel, W. (2016).
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DeVito, Nicholas J; Bacon, Seb; Goldacre, Ben (February 2020).
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Dickersin, K; Rennie, D (2009). "Registering clinical trials".
4010:"Research registries: Facts, myths, and possible improvements" 2958: 2366:"As ClinicalTrialsgov Turns 10 Will We See Compliance Improve" 645: 568:, p. 2605). This argument assumes that non-preregistered 148: 3923: 708: 684: 3874:"Questionable research practices following pre-registration" 3305: 3303: 2977: 2975: 1976: 4568: 4268:
L. Haven, Tamarinde; Van Grootel, Dr. Leonie (2019-04-03).
1096:"Registered Reports: A new publishing initiative at Cortex" 434: 87: 4559:
Preregistration resources from the Centre for Open Science
3823:"Ensuring the quality and specificity of preregistrations" 3147:
Advances in Methods and Practices in Psychological Science
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Chambers, C. D.; Forstmann, B.; Pruszynski, J. A. (2019).
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Advances in Methods and Practices in Psychological Science
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Advances in Methods and Practices in Psychological Science
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Ikeda, A.; Xu, H.; Fuji, N.; Zhu, S.; Yamada, Y. (2019).
3720: 3718: 2172:"Compliance with Results Reporting at ClinicalTrials.gov" 2110:"International Clinical Trials Registry Platform (ICTRP)" 2062:
GĂĽlmezoglu, AM; Pang, T; Horton, R; Dickersin, K (2005).
1729:"International Clinical Trials Registry Platform (ICTRP)" 444: 4228: 4032: 4030: 3917: 3915: 3633: 3631: 921:"A community-sourced glossary of open scholarship terms" 604:). Hence, although preregistraton is supposed to reduce 3561:"Increasing transparency through a multiverse analysis" 3451:"Paths in strange spaces: A comment on preregistration" 2389:
Journal of the American Medical Informatics Association
3893: 3891: 3640:"The case for formal methodology in scientific reform" 1788:"Major Journals Press for Clinical Trial Registration" 1182:
Allen, Christopher; Mehler, David M. A. (1 May 2019).
4563: 4188:
Simmons, J. P.; Nelson, L. D.; Simonsohn, U. (2021).
2673: 2491:
Kimmelman, Jonathan; Anderson, James A. (June 2012).
1671:"Refining animal research: The Animal Study Registry" 1397:
Weston, S. J.; Ritchie, S. J.; Rohrer, J. M. (2019).
846: 844: 842: 840: 838: 836: 468: 467:
Over 200 journals offer a registered reports option (
3390:
Organizational Behavior and Human Decision Processes
3384:Collins, H.K.; Whillans, A. V.; John, L. K (2021). 2787:"Promoting reproducibility with registered reports" 269:
Food and Drug Administration Amendments Act of 2007
3205:Krishna, Anand; Peter, Sebastian M. (2018-08-30). 310:International Committee of Medical Journal Editors 284:International Committee of Medical Journal Editors 262:International Committee of Medical Journal Editors 1340:"Preregistration of analyses of preexisting data" 1530:Paul, M.; Govaart, G. H.; Schettino, A. (2021). 1491:"Preregistration in single-case design research" 3503: 3501: 3499: 3497: 857:Proceedings of the National Academy of Sciences 735:and make any residual flexibility transparent ( 292:International Clinical Trials Registry Platform 4008:Abrams, E.; Libgober, J.; List, J. A. (2020). 2266:Pullar, T; Kumar, S; Feely, M (October 1989). 751:method and analyses than in the rationale for 4039:"Preregistration: Comparing dream to reality" 8: 2984:"An agenda for purely confirmatory research" 545:Journal of Political Economy: Microeconomics 3278:Journal of Political Economy Microeconomics 2493:"Should preclinical studies be registered?" 2899:Martin, G. N.; Clarke, Richard M. (2017). 209:United States National Library of Medicine 4479: 4469: 4428: 4335: 4285: 4164: 4154: 4113: 4064: 4054: 3964: 3903: 3848: 3838: 3789: 3654: 3576: 3535: 3525: 3360: 3327: 3248: 3230: 3116: 2934: 2916: 2875: 2857: 2802: 2753: 2704: 2648: 2591: 2573: 2524: 2467: 2449: 2408: 2340: 2291: 2195: 1704: 1686: 1645: 1635: 1594: 1557: 1547: 1536:International Journal of Psychophysiology 1506: 1465: 1424: 1414: 1365: 1355: 1314: 1297:Haven, T. L.; Van Grootel, D. L. (2019). 1209: 1199: 944: 886: 876: 741:high quality theory and research practice 4361:"What should a preregistration contain?" 415: 408:Overview of preclinical study registries 337: 3514:The Quantitative Methods for Psychology 3425:"Preregistration: A plan, not a prison" 1094:Chambers, Christopher D. (March 2013). 987:. Association for Psychological Science 832: 4537: 4526: 4393: 4382: 3704: 3693: 3483: 3472: 2738:"Replication in Psychological Science" 1786:Barrett, Stephen (13 September 2004). 1279: 1268: 4270:"Preregistering qualitative research" 3946: 3944: 3565:Perspectives on Psychological Science 3386:"Joy and rigor in behavioral science" 3343:Coffman, L. C.; Niederle, M. (2015). 3184:. Maidenhead: Open University Press. 2988:Perspectives on Psychological Science 1338:Mertens, G.; Krypotos, A. M. (2019). 1299:"Preregistering qualitative research" 756:guidance on what to include and why ( 325:Overview of clinical trial registries 111:Quantitative research in psychology ( 7: 1489:Johnson, A. H.; Cook, B. G. (2019). 644:; for several other approaches, see 3058:Journal of Business and Psychology 2736:Lindsay, D. Stephen (2015-11-09). 396:Australia and New Zealand (ANZCTR) 215:(CRO) which is running the study. 25: 3678:Szollosi, A.; Donkin, C. (2019). 3310:Nosek, B. A.; Lakens, D. (2014). 3180:Pennington, Charlotte R. (2023). 2383:Huser, V.; Cimino, J. J. (2013). 331:List of clinical trial registries 4156:10.1001/jamaophthalmol.2019.0312 3988: 3727:"Is preregistration worthwhile?" 3349:Journal of Economic Perspectives 2693:European Journal of Neuroscience 2272:Annals of the Rheumatic Diseases 2129:Journal of Clinical Epidemiology 985:"Registered Replication Reports" 853:"The preregistration revolution" 303:http://apps.who.int/trialsearch/ 4411:Pham, M. T.; Oh, T. T. (2020). 2846:Frontiers in Human Neuroscience 2268:"Compliance in clinical trials" 2176:New England Journal of Medicine 500:European Journal of Personality 370:Japan registries network (JPRN) 188:before they are performed in a 184:is the practice of documenting 147:Electroencephalogram research ( 4417:Journal of Consumer Psychology 4194:Journal of Consumer Psychology 2141:10.1016/j.jclinepi.2019.09.005 1891:10.1080/01621459.1959.10501497 213:contract research organization 1: 4287:10.1080/08989621.2019.1580147 3878:Japanese Psychological Review 3038:Japanese Psychological Review 2959:"Registered Reports Overview" 2364:Miseta, Ed (9 January 2018). 2237:10.1016/S0140-6736(19)33220-9 2080:10.1016/s0140-6736(05)66589-0 1316:10.1080/08989621.2019.1580147 1007:Japanese Psychological Review 762:Haven & Van Grootel, 2019 733:researcher degrees of freedom 606:researcher degrees of freedom 590:Collins et al., 2021, Study 1 469:Centre for Open Science, 2019 244:FDA Modernization Act of 1997 127:Mertens & Krypotosm, 2019 120:Haven & Van Grootel, 2019 3840:10.1371/journal.pbio.3000937 3731:Trends in Cognitive Sciences 3232:10.1371/journal.pone.0203470 2575:10.1371/journal.pone.0223758 2451:10.1371/journal.pbio.2000391 1688:10.1371/journal.pbio.3000463 1637:10.1371/journal.pbio.3000690 1201:10.1371/journal.pbio.3000246 1115:10.1016/j.cortex.2012.12.016 737:Simmons et al., 2021, p. 180 586:Coffman & Niederle, 2015 3905:10.1101/2021.03.12.21253378 3402:10.1016/j.obhdp.2021.03.002 2401:10.1136/amiajnl-2012-001501 2333:10.1136/bmjopen-2015-009758 811:Clinical trial registration 658:Szollosi & Donkin, 2019 278:International participation 182:Clinical trial registration 177:Clinical trial registration 103:Specialised preregistration 35:Clinical trial registration 4620: 4450:Royal Society Open Science 4274:Accountability in Research 4043:Royal Society Open Science 3966:10.3758/s13428-023-02277-0 3800:10.1007/s11229-021-03276-4 3743:10.1016/j.tics.2019.11.009 3089:Royal Society Open Science 3070:10.1007/s10869-020-09695-3 2840:Yeung, Andy W. K. (2017). 1303:Accountability in Research 937:10.1038/s41562-021-01269-4 766:Van den Akker et al., 2021 725:Van den Akker et al., 2023 697:Van den Akker et al., 2023 328: 135:van den Akker et al., 2021 3957:Behavior Research Methods 3656:10.1101/2020.04.26.048306 3329:10.1027/1864-9335/a000192 3159:10.1177/25152459231202724 2961:. Center for Open Science 2672:Centre for Open Science. 2633:10.1136/bmjos-2019-100051 2114:World Health Organization 1559:21.11116/0000-0008-2B30-2 1235:The American Psychologist 1169:10.1177/25152459211007467 1142:10.1027/1864-9335/a000192 288:World Health Organization 221:World Health Organization 56:, inappropriate forms of 4604:Evidence-based practices 3578:10.1177/1745691616658637 3000:10.1177/1745691612463078 2918:10.3389/fpsyg.2017.00523 2859:10.3389/fnhum.2017.00468 2755:10.1177/0956797615616374 1508:10.1177/0014402919868529 1416:10.1177/2515245919848684 616:-hacking and unreported 602:Wagenmakers et al., 2012 598:Nosek & Lakens, 2014 558:Nosek & Lakens, 2014 533:Wagenmakers et al., 2012 260:Shortly thereafter, the 227:Creation and development 190:clinical trials registry 142:Johnson & Cook, 2019 77:Standard preregistration 18:Clinical trials registry 3600:Srivastava, S. (2018). 3537:10.20982/tqmp.16.4.p376 3429:Centre for Open Science 2905:Frontiers in Psychology 2804:10.1038/s41562-016-0034 1081:10.1525/collabra.117094 878:10.1073/pnas.1708274114 620:that leads to inflated 562:Centre for Open Science 513:Center for Open Science 425:Animalstudyregistry.org 296:Declaration of Helsinki 4536:Cite journal requires 4392:Cite journal requires 4359:McPhetres, J. (2020). 3703:Cite journal requires 3482:Cite journal requires 2791:Nature Human Behaviour 2370:www.clinicalleader.com 1954:10.1001/jama.2012.4230 1848:10.1001/jama.290.4.516 1823:on September 17, 2008. 1163:(2): 251524592110074. 1034:Psychological Bulletin 1019:10.24602/sjpr.62.3_221 925:Nature Human Behaviour 789:Soderberg et al., 2020 713:Boghdadly et al., 2018 622:familywise error rates 492:Nature Human Behaviour 161:Exploratory research ( 118:Qualitative research ( 84:Open Science Framework 4513:10.31222/osf.io/7x9vy 4369:10.31234/osf.io/cj5mh 4337:10.15626/MP.2020.2625 4241:10.31222/osf.io/epgjd 4056:10.31234/osf.io/d8wex 3688:10.31234/osf.io/suzej 3649:: 2020.04.26.048306. 3614:10.31234/osf.io/bwr48 3459:10.31234/osf.io/wxn58 2742:Psychological Science 2284:10.1136/ard.48.10.871 2188:10.1056/NEJMsa1409364 1596:10.31234/osf.io/seyq7 1549:10.31234/osf.io/4tgve 1467:10.15626/MP.2020.2625 1247:10.31234/osf.io/d7m5r 785:Szollosi et al., 2020 670:Szollosi et al., 2020 480:Psychological Science 473:Chambers et al., 2019 154:Experience sampling ( 140:Single case designs ( 3784:(3–4): 10969–11000. 3772:Rubin, Mark (2021). 3449:Navarro, D. (2020). 2497:Nature Biotechnology 1915:Clin Trials Metaanal 1618:Dirnagl, U. (2020). 1495:Exceptional Children 1344:Psychologica Belgica 1069:Collabra: Psychology 773:Devezer et al., 2020 729:Claesen et al., 2019 709:Heirene et al., 2021 705:Claesen et al., 2019 685:Heirene et al., 2021 650:Devezer et al., 2020 642:Steegen et al., 2016 542:A 2024 study in the 455:Preclinicaltrials.eu 317:Reporting compliance 156:Kirtley et al., 2019 113:Bosnjak et al., 2021 4471:10.1098/rsos.181351 4462:2020RSOS....781351F 4017:NBER Working Papers 3362:10.1257/jep.29.3.81 3223:2018PLoSO..1303470K 3109:10.1098/rsos.211997 3101:2022RSOS....911997S 3029:Lakens, D. (2019). 2785:Mellor, D. (2017). 2566:2019PLoSO..1423758W 2074:(9474): 1829–1831. 1768:on October 12, 2008 869:2018PNAS..115.2600N 781:Pham & Oh, 2020 758:Bowman et al., 2016 701:Abrams et al., 2020 681:Bakker et al., 2020 417: 198:selective reporting 131:Weston et al., 2019 27:Scientific practice 4143:JAMA Ophthalmology 4115:10.1111/anae.14103 3508:Rubin, M. (2020). 2829:. 6 February 2018. 2231:(10221): 361–369. 1977:"SANCTR > Home" 1792:www.quackwatch.org 793:Field et al., 2020 717:Singh et al., 2021 693:Singh et al., 2021 689:Ikeda et al., 2019 594:Nosek et al., 2018 578:Nosek et al., 2018 566:Nosek et al., 2018 529:Nosek et al., 2018 416: 344:ClinicalTrials.gov 240:ClinicalTrials.gov 205:ClinicalTrials.gov 125:Preexisting data ( 94:Registered reports 66:replication crisis 39:registered reports 4430:10.1002/jcpy.1209 4206:10.1002/jcpy.1207 3316:Social Psychology 3191:978-0-335-25116-2 2706:10.1111/ejn.14319 2182:(11): 1031–1039. 2049:www.anzctr.org.au 1981:www.sanctr.gov.za 1130:Social Psychology 863:(11): 2600–2606. 460: 459: 405: 404: 170:Bert et al., 2019 168:Animal Research ( 149:Paul et al., 2021 58:post hoc analysis 16:(Redirected from 4611: 4546: 4545: 4539: 4534: 4532: 4524: 4500: 4494: 4493: 4483: 4473: 4441: 4435: 4434: 4432: 4408: 4402: 4401: 4395: 4390: 4388: 4380: 4356: 4350: 4349: 4339: 4314: 4308: 4307: 4289: 4265: 4259: 4258: 4256: 4255: 4224: 4218: 4217: 4185: 4179: 4178: 4168: 4158: 4134: 4128: 4127: 4117: 4093: 4087: 4086: 4068: 4058: 4034: 4025: 4024: 4014: 4005: 3999: 3992: 3986: 3968: 3948: 3939: 3938: 3936: 3934: 3919: 3910: 3909: 3907: 3895: 3886: 3885: 3869: 3863: 3862: 3852: 3842: 3833:(12): e3000937. 3818: 3812: 3811: 3793: 3769: 3763: 3762: 3722: 3713: 3712: 3706: 3701: 3699: 3691: 3675: 3669: 3668: 3658: 3644: 3635: 3626: 3625: 3597: 3591: 3590: 3580: 3556: 3550: 3549: 3539: 3529: 3505: 3492: 3491: 3485: 3480: 3478: 3470: 3446: 3440: 3439: 3437: 3435: 3420: 3414: 3413: 3381: 3375: 3374: 3364: 3340: 3334: 3333: 3331: 3307: 3298: 3297: 3269: 3263: 3262: 3252: 3234: 3202: 3196: 3195: 3177: 3171: 3170: 3137: 3131: 3130: 3120: 3080: 3074: 3073: 3052: 3046: 3045: 3035: 3026: 3020: 3019: 2979: 2970: 2969: 2967: 2966: 2955: 2949: 2948: 2938: 2920: 2896: 2890: 2889: 2879: 2861: 2837: 2831: 2830: 2823: 2817: 2816: 2806: 2782: 2776: 2775: 2757: 2733: 2727: 2726: 2708: 2684: 2678: 2677: 2669: 2663: 2662: 2652: 2621:BMJ Open Science 2612: 2606: 2605: 2595: 2577: 2560:(11): e0223758. 2545: 2539: 2538: 2528: 2509:10.1038/nbt.2261 2488: 2482: 2481: 2471: 2453: 2444:(11): e2000391. 2429: 2423: 2422: 2412: 2380: 2374: 2373: 2361: 2355: 2354: 2344: 2312: 2306: 2305: 2295: 2263: 2257: 2256: 2216: 2210: 2209: 2199: 2167: 2161: 2160: 2124: 2118: 2117: 2106: 2100: 2099: 2059: 2053: 2052: 2041: 2035: 2034: 2032: 2031: 2022:. 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Index

Clinical trials registry
p-hacking
publication bias
data dredging
post hoc analysis
HARKing
replication crisis
Open Science Framework
AsPredicted
Bosnjak et al., 2021
Haven & Van Grootel, 2019
Mertens & Krypotosm, 2019
Weston et al., 2019
van den Akker et al., 2021
Johnson & Cook, 2019
Paul et al., 2021
Kirtley et al., 2019
Dirnagl, 2020
Bert et al., 2019
clinical trials
publication bias
selective reporting
ClinicalTrials.gov
United States National Library of Medicine
contract research organization
World Health Organization
ClinicalTrials.gov
FDA Modernization Act of 1997
Eliot Spitzer
GlaxoSmithKline

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