Public Funding and Open Access to Research: A Review of Canadian Multiple Sclerosis Research

Public Funding and Open Access to Research: A Review of Canadian Multiple Sclerosis Research

Public Funding and Open Access to Research: A Review of Canadian Multiple Sclerosis Research

Original Paper

1Health Sciences Libraries, University of Minnesota, Minneapolis, MN, United States

2Council of Prairie and Pacific University Libraries, Vancouver, BC, Canada

3Hotchkiss Brain Institute and the Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada

4Library, Wilfrid Laurier University, Waterloo, ON, Canada

Corresponding Author:

Caitlin Bakker, MLIS

Health Sciences Libraries

University of Minnesota

303 Diehl Hall, 505 Essex Street SE

Minneapolis, MN,

United States

Phone: 1 612 301 1353

Fax:1 612 626 2454

Email: cjbakker@umn.edu


Background: Multiple sclerosis (MS), a progressive demyelinating disease of the brain and spinal cord, is the leading cause of nontraumatic neurological damage in young adults. Canada has one of the highest reported incidents of MS, with estimates between 55 and 240 per 100,000 individuals. Between 2009 and 2014, the MS Society of Canada provided over Can $90 million to researchers and, since 2013, has encouraged researchers to make both current and previous research products openly available.

Objective: The goal of the study was to determine the open access (OA) cost implications and repository policies of journals frequently used by a sample of MS researchers. This study benchmarked current publishing preferences by MS Society of Canada researchers by examining the OA full-text availability of journal articles written by researchers funded between 2009 and 2014.

Methods: Researchers were identified from the 2009 to 2014 annual MS Society of Canada Research Summaries. Articles were identified through searches in Web of Science, Scopus, Medline and Embase (both via OVID). Journal level analysis included comparison of OA policies, including article processing charges (APCs) and repository policies. Data were analyzed using descriptive statistics.

Results: There were 758 articles analyzed in this study, of which 288 (38.0%) were OA articles. The majority of authors were still relying on journal policies for deposit in PubMed Central or availability on publisher websites for OA. Gold OA journals accounted for 10.2% of the journals in this study and were associated with significantly lower APCs (US $1900) than in hybrid journals (US $3000). Review of the journal self-archiving options highlighted the complexity of stipulations that authors would have to navigate to legally deposit a version of their article.

Conclusions: This study found that there are currently researcher- and publisher-imposed barriers to both the gold and green roads to OA. These results provide a current benchmark against which efforts to enhance openness can be measured and can serve as a reference point in future assessments of the impact of OA policies within this field. With funding agencies worldwide releasing OA mandates, future success in compliance will require changes to how researchers and publishers approach production and dissemination of research.

J Med Internet Res 2017;19(2):e52

doi:10.2196/jmir.6250

Keywords



Multiple sclerosis (MS), a progressive demyelinating disease of the brain and spinal cord, is the leading cause of nontraumatic neurological damage in young adults [1]. Depending on the affected areas of the brain, balance, vision, hearing, thinking, and memory may ultimately be impacted. Canada has one of the highest reported incidents of MS, with estimates between 55 and 240 per 100,000 individuals [2]. Despite over 200 years of research and significant recent findings [3], a standard, evidence-based treatment proven to halt the chronic progression and long-term disability has remained elusive. Given the debilitating character of MS and its prevalence in Canada, it is not surprising that the MS Society of Canada infuse significant funding to advance research. Between 2009 and 2014, the MS Society of Canada provided over Can $90 million to researchers in four major research areas: (1) symptom management and quality of life, (2) progression and therapies, (3) cause and risk factors, and (4) nerve damage and repair [4].

The MS Society of Canada has strongly encouraged open access (OA) and the broad dissemination of research. The MS Society of Canada’s OA policy, which came into effect in July 2013, requires grant recipients to make every effort to ensure their peer-reviewed publications are available OA within 6 months of publication [5]. While the policy came into effect in 2013, the MS Society of Canada encourages retroactive compliance for research funded before that date.

The information needs and information-seeking behaviors of clinicians and patients with MS have been well documented [6-10]. Studies have shown that MS patients are demanding active roles in their treatments and the decision-making process [11-13], and health care information on the Internet ranks second to health professionals as a source of information for patients [14]. Although scientists and funding agencies recognize the potential public value of research and of making work available OA, resources are required to facilitate the process. Whether these are financial resources to pay for article processing charges (APCs) or the time to negotiate with journals to allow for deposit in an appropriate repository, OA requires work on the part of the researcher. The appropriate allocation of resources for broad dissemination remains a question.

Using the MS Society of Canada as a case study, this paper examines the OA full-text availability of scientific articles by Canadian researchers funded between 2009 and 2014, including the publishing venues and associated costs of making work openly available. The goal of the study was to determine the extent of OA, the cost implications, and repository policies of journals frequently used by MS researchers as an assessment of the current context which can be used in future evaluations of the extent of openness and the effectiveness of mandates in making research OA.


Database Search

Researchers were identified from the 2009 to 2014 annual MS Society of Canada Research Summaries [15]. Researcher names and affiliations, titles of the research projects, funded amounts, and funded years were recorded in an Excel (Microsoft) file. The name of the researcher and the keyword “Multiple Sclerosis” were searched in 4 databases: Web of Science, Scopus, and Embase and Medline (both via OVID platform). Due to the inconsistencies in funding information in journal metadata, searches did not incorporate the MS Society of Canada as a funding body. In selected cases, an author affiliation was used to aid in disambiguation. Publications were limited to the first year the researcher received MS Society funding and all subsequent years. Articles published in 2015 were included in this analysis to account for the time necessary to finalize research, write publications, and complete the publishing process. Publication types were limited to journal articles, review articles, and conference papers reproduced in their entirety in a journal, including items that were both published and in press. Searches were limited to English language only.

The results from the database searches were merged into a single, deduplicated file of articles. A secondary quality check was performed by manually reviewing the article details to ensure relevance and accuracy. The article title was searched in Google and PubMed to determine if the full-text was openly accessible (open access) either through the publisher website or PubMed Central. The journal policy for access through PubMed Central and the version of the article on PubMed Central (author manuscript to meet compliance with a funder policy or a journal OA policy) were recorded. Full-text access through other sources such as Academia.edu or ResearchGate was not included because these sites do not necessarily guarantee that the full-text option is a legitimate copy.

Colors to Categorize Policies

Subscription policies were used to identify the title as a pure gold journal or a hybrid journal. The self-archiving policies for each journal were obtained from SHERPA RoMEO, a UK academic supported database that provides information regarding copyright policies and rights retained by the authors when publishing in specific academic journals. SHERPA RoMEO uses colors to categorize publishers’ archiving policies: white (archiving is not formally supported), yellow (authors can archive preprint, that is, prerefereeing), blue (authors can archive postprint, that is, final draft postrefereeing, or publisher's version), or green (authors can archive preprint and postprint, or publisher's version). Each journal in the study was assigned one of the 4 colors. The OA policies were analyzed first by publisher, per journal, and then at the article level.

For each journal, APC policies were searched on the publisher website. APC costs were also converted to US dollars. The maximum APC fee quoted by the journal was recorded where there were variable fees listed. APCs fees were variable depending on the type of article, memberships, institutional affiliations, funding bodies, or which Creative Commons license was selected.


Overview of Publishing Venues

The MS Society of Canada funded 77 Canadian researchers between 2009 and 2014 in one of their four major research areas. This study identified a total of 758 MS related articles in 211 journals produced by 61 publishers. Of the 758 articles, 288 (38.0%) were OA articles produced in 93 journals by 42 publishers.

When article distribution per journal was analyzed to identify the preferred or most popular publishing venues, there was a noticeable difference in the dominance of publishers. Three major publishers (Elsevier, Wiley, and Springer Nature) dominated the research output, with 105 of 211 journals (49.7%) and 374 of 758 articles (49.3%). However, these publishers only accounted for 93 of the 288 OA articles (32.2%) in the study (Figure 1). Only one Elsevier journal (NeuroImage: Clinical) and 3 Springer journals (BMC Health Services Research, BMC Neurology, and Journal of Neuroinflammation) were pure gold in which every article was OA full-text upon publication. There were no pure gold journals from Wiley-Blackwell identified in the articles analyzed in this study.

A total of 19 journals from 13 publishers accounted for 388 of the 758 articles (51.2%) and 146 of the 288 OA articles (50.7%) in the study (Table 1). The three major publishers (Elsevier, Wiley, and Springer Nature) published 8 of the 19 journals in this preferred grouping, but SAGE and Lippincott Williams and Wilkins (LWW) were the top publishers with both their journals, Multiple Sclerosis (SAGE) and Neurology (LWW) accounting for 142 of the 758 articles (18.7%) in the study. Only one pure gold journal (PLoS ONE) was in this grouping, ranking 11th, with 14 of the 758 articles in the study (Table 1).

Table 1. The most frequently used journals, accounting for 51.2% of the articles. Number of articles, number of open access (OA) articles, article processing charges (APC), and SHERPA RoMEO color are provided.
Journal titleArticles (n)OA articles (n)Maximum APC (US $)SHERPA RoMEO color
Multiple Sclerosis76153000Green
Neurology66353100Yellow
Journal of the Neurological Sciences2302500Green
Annals of Neurology2343000Yellow
GLIA1923000Yellow
Journal of Neuroimmunology1822500Green
Multiple Sclerosis and Related Disorders1822500Green
Journal of Neurology1773000Green
Journal of Immunology16143000Blue
Lancet Neurology1605000Green
PLoS ONE14141350Green
Canadian Journal of Neurological Sciences1302000Green
NeuroImage1322200Green
Journal of Neurology, Neurosurgery and Psychiatry1072822Green
Journal of Neuroscience10102820Yellow
International Journal of MS Care99n/aUngraded
Neuro-epidemiology963250Green
Brain973200Yellow
JAMA Neurology (Archives of Neurology)98n/aWhite
Figure 1. The top three publishers by journal and article count.
View this figure

Article Processing Charges

A closer examination of the reason for the availability of OA revealed limited use of APC payments or deposit of author manuscripts in PubMed Central, even though most journals offered these as options (see Figure 2). Of the 288 OA articles, 180 (62.5%) were made available in their final typeset form, either through deposit in PubMed Central (163/180, 90.6%) or through the publisher’s website (17/180, 9.4%) without evidence of APC payment. In comparison, author directed OA through APCs accounted for 77 of the 288 articles (26.7%), whereas 31 of the 288 articles (10.8%) were made available as manuscripts deposited in PubMed Central. The limited use of APCs is even more striking when all articles in the study are considered. Whereas 662 of the 758 articles were published in journals with APC options, only 77 of the 758 (10.2%) have been published using that option.

APCs for pure gold and hybrid journals revealed significant differences in potential costs to authors. Of the 211 journals in this study, 22 were pure gold, with each of the 60 articles produced by these journals freely available full-text upon publication. Pure gold journals not only use APCs to cover publication costs but also use institutional memberships or other funding options to provide all content openly accessible upon publications. The pure gold journals in this study had variable APCs depending on memberships, government support, and the type of article published. APCs were listed on publisher sites for 19 of the 22 journals. One of these unlisted journals (Preventing Chronic Disease) was produced by the Centers for Disease Control and Prevention which does not use APCs. Functional Neurology and European Neurological Review also did not list APCs in their author instructions. For the 19 journals for which APCs were found, the average and mode fees were US $1900.

APCs were found for 137 of the 189 hybrid journals. The other 52 journals either required authors to contact the publisher for fee information or it was not evident if the option existed. Fees within a journal could vary depending on memberships, institutional affiliations, funding bodies, or which Creative Commons license was selected. The APCs ranged from US $600 to US $5000. The APC fees were notably higher for hybrid journals than for pure gold journals. The average cost was US $2800, and the mode was US $3000. The APCs for the hybrid journals with the highest number of articles in this study ranged from US $1000 for members in the Canadian Journal of Neurological Sciences to US $5000 for Lancet Neurology. Table 2 provides a profile of the potential APC costs for articles from this study published in 2014.

Table 2. Snapshot of maximum article processing charges (APCs) for articles published in 2014.
Journal TypeNAPCa Information
JournalsArticlesRangeAverageMode
Journals without APC information1822N/AN/AN/A
Gold journals with APCs916US $1350 to US $2310US $1735US $1500
Hybrid journals with APCs54108US $600 to US $5000US $2979US $3000

aAPC: article processing charge.

Figure 2. The number of final articles available as open access due to article processing charge (APC) payments, article manuscript deposit in PubMed Central, and final articles available without evidence of APC payment through deposit of published articles to PubMed Central or availability from the publisher website.
View this figure

Policies for and Prevalence of Self-Archiving

With the impracticability of the APC model for many researchers, the policies for self-deposit were reviewed for the 211 journals in the study. The SHERPA RoMEO website provided information on journal policies for 203 of 211 journals in the study. The ability for authors to self-archive a preprint or postprint of the article to an institutional or subject-based repository was offered by the majority of journals, but there was large variability in the version of the manuscript that could be deposited.

Of the 211 journals, 120 allowed deposit of the final draft (postprint) of the manuscript, 71 allowed the final draft but with additional restrictions, and 11 did not allow the final draft and information was not provided the other 9 journals. The SHERPA RoMEO analysis identified deposit embargoes on 138 of the journals that would have affected 564 of the 758 articles in this study (74%). In addition, the restrictive self-archiving policies (yellow and white SHERPA RoMEO categories) were applied to journals produced by 16 societies.

Of the 77 MS Society of Canada funded researchers included in this study, 62 had affiliations that would offer access to an institutional repository (IR). A secondary search of repositories for the 760 articles found that 8 of the 760 articles (1%) identified in this study were made available through an IR. Of these, all 8 were originally published in pure gold journals, namely in BioMed Central titles. IRs did not appear to function as a mechanism to make otherwise inaccessible content publicly available.


Principal Findings

Despite encouragement from the public and the clinical community [16-18], and the MS Society of Canada’s goal of making both current and previous research publicly available, the overall rates of openness in MS research remains low. Of the 758 articles included in this study, only 288 are currently available OA. This finding acts as a current benchmark against which the efforts to enhance openness and dissemination can be measured, and can serve as a reference point when assessing the impact of OA policies in this field.

The Cost of Open Access

The hybrid gold model is fraught with cost implications to both the individual researcher and institutions. The monopoly of hybrid journal ownership by the big three commercial publishers (Elsevier, Wiley, and Springer Nature) has serious implications for the openness of research findings. In this study, these 3 publishers controlled 49.7% of the journals (105/211), 49.3% of the article output (374/758), and the majority (96/105, 91.4%) of their journals followed the hybrid model.

The hybrid model had been developed as a compromise between subscription publishers and OA advocates [19]. However, it has underperformed, with less than 2% of eligible authors making work available in this manner [20]. Our study confirmed the low use of APCs, with 10% of eligible articles being made available with this option. In a recent survey of Canadian scientists, 78% felt that publishing OA was unaffordable and 86% felt that funding for OA publishing was not readily available [21]. Recent studies continue to report that lack of funds for APCs is an impediment to publishing in OA or hybrid journals [22-24].

The mode APC cost for hybrid journals was US $3000, which was 45% higher than for pure gold journals, a finding which is consistent with other recent research [25,26]. The impact of high APC costs and institutions costs has notable economic consequences in Canada, where the majority of researchers and universities are publicly funded. Academic libraries pay publishers large fees for institutional subscriptions to journals then authors pay the same publishers additional APC costs to publish their article in those same journals. In effect, there is “double dipping” of public funding, especially in the context where Canadian universities are subscribing to the “big journal deals” with all the major publishers, through the Canadian Knowledge Research Network (CRKN). In this Canadian-context study, it is also important to consider that these figures represent US dollar calculations and that exchange rate fluctuations add additional burdens to fund APCs.

Pure Gold Publication Patterns

The pure gold road to OA is not a road well-travelled by MS researchers. Pure gold journals accounted for 7.9% (60/758) of the articles and 10.4% (22/211) of the journals in this study. Although this study showed evidence of the use of pure gold journals by the researcher, the low number of articles in these venues may indicate that MS researchers feel that OA is poorly regulated, of poor quality, and lacking in peer review. This would support previous research that has found that despite awareness of OA and OA issues, faculty concerns about quality, reputation, copyright, plagiarism, and a perceived lack of peer review remained constant [27,28]. The appearance of PLoS ONE, ranked 11th based on article count of the 211 journals, is a promising evidence of the growing influence of gold OA.

Barriers to Green Open Access

Self-archiving is the most cost-effective method of providing OA to research findings for researchers. Local self-archiving includes depositing a postprint or preprint of the article in an IR or self-archiving in a subject repository. However, rather than offering a simplified option, publishers have created barriers to OA through unsustainable complexities involved in self-archiving policies. Of the 35 professional society or association journals represented in this study, 15 had restrictive yellow self-archiving policies. Yellow self-archiving only allows authors to post the prerefereed preprint. With peer review considered the most important criteria in journal publishing, there is potentially little value to the open communication of research of an article without peer review [29,30].

Poltronieri et al [31] also found that in their survey of journals, more than half of the publishers are still imposing yellow and white restrictions on self-archiving. Even among green journals, navigating restrictions and permissions is challenging. In addition to the version requirements of the publisher, there were additional requirements regarding embargo periods, restricting when the self-archived version could be made available. The journal embargoes were often listed as a set of complex conditions that authors would need to navigate to comply with the journal’s requirements for self-archiving.

Future Directions

The solution to resistance, either from journals or researchers, is sometimes assumed to be the requirements from funding sources or institutions [32,33]. Mandated public access from funding agencies, principally National Institutes of Health (NIH), has led to tremendous growth in the availability of biomedical literature [34]. However, the NIH, despite having an OA policy written into law 2008, found that low compliance continued to be a major issue. Researchers had indicated that a lack of time, a frustrating deposit process, and confusing journal policies were the primary reasons for lack of compliance [35]. NIH introduced a policy delaying applications and funding if publications associated with the research were not in compliance. Following this, NIH saw aggregate submissions increase from an average of 5158 articles per month in 2012 to 7931 articles per month in 2013 and 7057 in 2014 [36]. Although NIH operates in a much different context than the MS Society of Canada, the NIH experience highlights that the requirement itself is not a sufficient motivation to overcome perceived barriers to compliance. Policy enforcement is a necessary component in this process. Whereas the MS Society of Canada has implemented an OA policy, the mechanisms for enforcement are not explicitly outlined in that policy.

Whether mandated OA will move MS research to a more open dissemination environment remains to be seen. The movement to OA requires incentives for involvement [37]. In the case of researchers, for whom promotion and tenure decisions may be significantly impacted by the number of publications and the venue in which they are published, journal selection may be a critical choice. Authors select journals to publish in based on journal reputation, impact factor, and turnaround time to publication [22,28,38]. Watson [39] found that the authors are confused by the notion of OA, reluctant to participate, and confounded by the myriad of choices they are presented with when trying to publish OA.

Surveys have shown that researchers have generally favorable views of OA and its benefits for both the public and the scientific community [40,41]. However, there are challenges to making work available through both green and gold roads to OA. Initial challenges include informing researchers about the concept of OA itself, as many scientists and researchers have no direct mechanisms in place to become more informed about these issues and may not recognize the necessity of doing so [42].

Study Limitations

As this study relied on bibliographic analysis rather than contacting researchers directly to provide a list of articles, the 758 articles used in the analysis may not have been directly produced as a result of the MS Society of Canada funded research. Any participating authorship by the 77 researchers during the time of funding by the Society was included in the study as long as the article was related to the topic of MS.

Conclusions

The prevalence of OA literature produced by the MS Society of Canada researchers has remained consistently low between 2009 and 2014. Of the 758 articles, 288 are available OA. Most OA articles were made available without evidence of APC payment. Although APCs in hybrid journals was significantly higher than those associated with pure gold journals, the use of APCs for publication was low among this group.

The recent implementation of the MS Society of Canada’s OA policy may increase OA publication within this field. Future research should include prevalence of OA of newly funded research as a means of determining policy impact and effectiveness.

Acknowledgments

This work was supported by the Research Support Fund of Wilfrid Laurier University and Alberta Health Innovates.

Conflicts of Interest

None declared.

  1. Noseworthy JH, Lucchinetti C, Rodriguez M, Weinshenker BG. Multiple sclerosis. N Engl J Med 2000 Sep 28;343(13):938-952. [CrossRef] [Medline]
  2. Beck CA, Metz LM, Svenson LW, Patten SB. Regional variation of multiple sclerosis prevalence in Canada. Mult Scler 2005 Oct;11(5):516-519. [Medline]
  3. Atkins HL, Bowman M, Allan D, Anstee G, Arnold DL, Bar-Or A, et al. Immunoablation and autologous haemopoietic stem-cell transplantation for aggressive multiple sclerosis: a multicentre single-group phase 2 trial. Lancet 2016 Aug 06;388(10044):576-585. [CrossRef] [Medline]
  4. Wollin J, Dale H, Spenser N, Walsh A. What people with newly diagnosed MS (and their families and friends) need to know. Int J MS Care 2000;2(3):29-39 [FREE Full text] [CrossRef]
  5. Multiple Sclerosis Society of Canada. 2015. Operating Grant Policies   URL: https://mssociety.ca/uploads/files/og-policies-final-en.pdf [accessed 2016-06-08] [WebCite Cache]
  6. Narayanaswami P, Gronseth G, Dubinsky R, Penfold-Murray R, Cox J, Bever C, et al. The Impact of Social Media on Dissemination and Implementation of Clinical Practice Guidelines: A Longitudinal Observational Study. J Med Internet Res 2015;17(8):e193 [FREE Full text] [CrossRef] [Medline]
  7. Colombo C, Filippini G, Synnot A, Hill S, Guglielmino R, Traversa S, et al. Development and assessment of a website presenting evidence-based information for people with multiple sclerosis: the IN-DEEP project. BMC Neurol 2016 Mar 02;16:30 [FREE Full text] [CrossRef] [Medline]
  8. Koschack J, Weibezahl L, Friede T, Himmel W, Makedonski P, Grabowski J. Scientific versus experiential evidence: discourse analysis of the chronic cerebrospinal venous insufficiency debate in a multiple sclerosis forum. J Med Internet Res 2015 Jul 01;17(7):e159 [FREE Full text] [CrossRef] [Medline]
  9. Köpke S, Solari A, Khan F, Heesen C, Giordano A. Information provision for people with multiple sclerosis. Cochrane Database Syst Rev 2014 Apr 21(4):CD008757. [CrossRef] [Medline]
  10. Lejbkowicz I, Paperna T, Stein N, Dishon S, Miller A. Internet usage by patients with multiple sclerosis: implications to participatory medicine and personalized healthcare. Mult Scler Int 2010;2010:640749 [FREE Full text] [CrossRef] [Medline]
  11. Colombo C, Mosconi P, Confalonieri P, Baroni I, Traversa S, Hill SJ, et al. Web search behavior and information needs of people with multiple sclerosis: focus group study and analysis of online postings. Interact J Med Res 2014;3(3):e12 [FREE Full text] [CrossRef] [Medline]
  12. Heesen C, Kasper J, Segal J, Köpke S, Mühlhauser I. Decisional role preferences, risk knowledge and information interests in patients with multiple sclerosis. Mult Scler 2004 Dec;10(6):643-650. [Medline]
  13. Snyder J, Adams K, Crooks VA, Whitehurst D, Vallee J. “I knew what was going to happen if I did nothing and so I was going to do something”: faith, hope, and trust in the decisions of Canadians with multiple sclerosis to seek unproven interventions abroad. BMC Health Serv Res 2014 Sep 30;14:445 [FREE Full text] [CrossRef] [Medline]
  14. Marrie RA, Salter AR, Tyry T, Fox RJ, Cutter GR. Preferred sources of health information in persons with multiple sclerosis: degree of trust and information sought. J Med Internet Res 2013;15(4):e67 [FREE Full text] [CrossRef] [Medline]
  15. Multiple Sclerosis Society of Canada. 2016. Research Summaries   URL: https://mssociety.ca/about-our-research-program/research-we-fund [accessed 2016-06-08] [WebCite Cache]
  16. Gafson AR, Giovannoni G. CCSVI-A. A call to clinicans and scientists to vocalise in an Internet age. Mult Scler Relat Disord 2014 Mar;3(2):143-146. [CrossRef] [Medline]
  17. Pullman D, Zarzeczny A, Picard A. “Media, politics and science policy: MS and evidence from the CCSVI Trenches”. BMC Med Ethics 2013 Feb 12;14:6 [FREE Full text] [CrossRef] [Medline]
  18. Ghahari S, Forwell SJ. Social media representation of chronic cerebrospinal venous insufficiency intervention for multiple sclerosis. Int J MS Care 2016;18(2):49-57 [FREE Full text] [CrossRef] [Medline]
  19. Prosser D. From here to there: A proposed mechanism for transforming journals from closed to open access. Learn Publ 2003;16(3):163-166 [FREE Full text] [CrossRef]
  20. Björk B. The hybrid model for open access publication of scholarly articles: A failed experiment? J Am Soc Inf Sci Technol 2012;63(8):1496-1504 [FREE Full text] [CrossRef]
  21. Björk B, Solomon D. Open access versus subscription journals: a comparison of scientific impact. BMC Med 2012;10(1):73 [FREE Full text] [CrossRef] [Medline]
  22. Phase 5 Research. Canadian Science Publishing. 2014. Canadian Researchers' Publishing Attitudes and Behaviours   URL: http://www.cdnsciencepub.com/files/PDF/CSP_ResearcherAttitudes_March14_FINAL.pdf [accessed 2016-06-08] [WebCite Cache]
  23. Lwoga E, Questier F. Faculty adoption and usage behaviour of open access scholarly communication in health science universities. New Libr World 2014;115(3/4):116-139 [FREE Full text] [CrossRef]
  24. Togia A, Korobili S. ELPUB. Attitudes towards open access: a metasynthesis of the empirical literature   URL: http://elpub.scix.net/data/works/att/102_elpub2014.content.pdf [accessed 2016-06-08] [WebCite Cache]
  25. Pinfield S, Salter J, Bath P. The 'total cost of publication' in a hybrid open-access environment: Institutional approaches to funding journal-article proccessing charges in combination with subscriptions. J Am Soc Inf Sci Technol 2016;67(7):1751-1766 [FREE Full text]
  26. Solomon D, Björk B. Article processing charges for open access publication-the situation for research intensive universities in the USA and Canada. Peer J 2016;4:e2264 [FREE Full text] [CrossRef] [Medline]
  27. Xia J. A longitudinal study of scholars attitudes and behaviors toward open-access journal publishing. J Am Soc Inf Sci Technol 2010;61(3):615-624 [FREE Full text] [CrossRef]
  28. Lwoga ET, Questier F. Open access behaviours and perceptions of health sciences faculty and roles of information professionals. Health Info Libr J 2015 Mar;32(1):37-49. [CrossRef] [Medline]
  29. Moore G. University of Toronto. 2011. Survey of University of Toronto faculty awareness, attitudes and practices regarding scholarly communication: A preliminary report   URL: https://tspace.library.utoronto.ca/handle/1807/26446 [accessed 2016-06-08] [WebCite Cache]
  30. Austin A, Heffernan M, David N. Open Access to Knowledge (OAK) Law Project. 2008. Academic authorship, publishing agreements and open access: Survey results   URL: http://eprints.qut.edu.au/13623/1/13623_3.pdf [accessed 2016-06-08] [WebCite Cache]
  31. Poltronieri E, Bravo E, Camerini T, Ferri M, Rizzo R, Solimini R, et al. Where on earth to publish? A sample survey comparing traditional and open access publishing in the oncological field. J Exp Clin Cancer Res 2013;32:4 [FREE Full text] [CrossRef] [Medline]
  32. Harnad S. Open access to research: Changing researcher behavior through university and funder mandates. JeDEM 2011;3(1):33-41 [FREE Full text]
  33. Pinfield S. A mandate to self archive? The role of open access institutional repositories. Serials: The Journal for the Serials Community 2005 Mar 1;18(1):30-34. [CrossRef]
  34. Morrison H. The Imaginery Journal of Poetic Economics. 2015. Dramatic Growth of Open Access   URL: http://poeticeconomics.blogspot.ca/2015/06/dramatic-growth-of-open-access-june-30.html [accessed 2016-06-08] [WebCite Cache]
  35. Charbonneau DH, McGlone J. Faculty experiences with the National Institutes of Health (NIH) public access policy, compliance issues, and copyright practices. J Med Libr Assoc 2013 Jan;101(1):21-25 [FREE Full text] [CrossRef] [Medline]
  36. National Institutes of Health. 2015. Monthly Aggregate Submission Statistics   URL: http://www.nihms.nih.gov/stats/ [accessed 2016-06-08] [WebCite Cache]
  37. Parks R. The Faustian grip of academic publishing. J Econ Methodol 2010;9:317-335 [FREE Full text] [CrossRef]
  38. Kuchma I. Electronic Information for Libraries. 2011. Results of the SOAP survey: A preliminary overview of the situation in EIFL partner countries   URL: http://www.eifl.net/system/files/resources/201408/soap_survey_results_eifl.pdf [accessed 2016-06-08] [WebCite Cache]
  39. Watson M. When will 'open science' become simply 'science'? Genome Biol 2015;16:101 [FREE Full text] [CrossRef] [Medline]
  40. Dallmeier-Tiessen S, Darby R, Goerner B, Hyppoelae J, Igo-Kemenes P, Kahn D. Cornell University Library. 2011. Highlights from the SOAP project survey. What scientists think about open access publishing   URL: http://arxiv.org/abs/1101.5260 [accessed 2016-06-08] [WebCite Cache]
  41. Fry J, Probets S, Creaser C, Greenwood H, Spezi V, White S. Loughborough University Institutional Repository. 2011. PEER behavioural research: authors and users vis-a-vis journals and repositories. D4.2 final report   URL: https://dspace.lboro.ac.uk/dspace-jspui/bitstream/2134/12967/3/PEER_D4_final_report_29SEPT11.pdf [accessed 2016-06-08] [WebCite Cache]
  42. Moorhead LL, Holzmeyer C, Maggio LA, Steinberg RM, Willinsky J. In an age of open access to research policies: Physician and public health NGO staff research use and policy awareness. PLoS One 2015;10(7):e0129708 [FREE Full text] [CrossRef] [Medline]


APC: article processing charge
CRKN: Canadian Knowledge Research Network
IR: Institutional Repository
MS: multiple sclerosis
NIH: National Institutes of Health
OA: open access


Edited by G Eysenbach; submitted 21.06.16; peer-reviewed by J Till PhD, H Morrison; comments to author 17.11.16; revised version received 15.12.16; accepted 31.01.17; published 27.02.17

Copyright

©Caitlin Bakker, Carol Stephenson, Erin Stephenson, Debbie Chaves. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 27.02.2017.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.