Peer Review History
| Original SubmissionAugust 25, 2022 |
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PONE-D-22-23734A randomised controlled trial of email versus mailed invitation letter in a national longitudinal survey of physicians.PLOS ONE Dear Dr. Scott, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ============================== ACADEMIC EDITOR: Thank you for submitting your paper to our journal. We appreciate the effort and time you have invested in your research. After a thorough review, we believe your study has merit and potential to contribute to the field. In order to help you improve the quality of your manuscript, we have provided detailed feedback and suggestions. We kindly ask you to consider these comments and critiques carefully as you revise your paper. Addressing these points will not only strengthen the methodology and discussion but also enhance the overall clarity, organization, and significance of your study. Once you have made the necessary revisions, please resubmit your manuscript for further review. We look forward to receiving your revised paper and evaluating its potential for publication in our journal. Thank you for considering our feedback, and we hope to receive your revised manuscript soon. ============================== Please submit your revised manuscript by May 25 2023 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript:
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Kind regards, Fares Alahdab, MD, MSc Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and 2. Please provide additional details regarding participant consent. In the ethics statement in the Methods and online submission information, please ensure that you have specified what type you obtained (for instance, written or verbal, and if verbal, how it was documented and witnessed). If your study included minors, state whether you obtained consent from parents or guardians. If the need for consent was waived by the ethics committee, please include this information. Once you have amended this/these statement(s) in the Methods section of the manuscript, please add the same text to the “Ethics Statement” field of the submission form (via “Edit Submission”). For additional information about PLOS ONE ethical requirements for human subjects research, please refer to http://journals.plos.org/plosone/s/submission-guidelines#loc-human-subjects-research. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: No Reviewer #2: Yes Reviewer #3: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: No Reviewer #2: Yes Reviewer #3: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: No Reviewer #2: No Reviewer #3: No ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: I have several concerns about the current study such that I cannot recommend it for publication at PLOS one. First, the topic is about a survey method, and it is comparing existing methods (online vs. letter recruitment for survey) rather than an innovative method. The sample size is restricted to be physicians, and the effect that was found is extremely small (i.e., a difference in about 2% response rate) albeit significant, and it is confirming previous findings. Given these, I think this study is more suitable for a specialized journal on survey methods. Second, the study was “administered between August 2018 and April 2019” I don’t know what the policy of PLOS-one is about this issue, but some journals do not accept results from surveys that are more than 3 years old. Furthermore, given that the motivation for the current study is that similar studies use more than 10-year-old data and the authors argued for an increase in internet usage. As we all know a lot of things happened since April of 2019 with emails and zoom meetings serving as essential tools in our society, so I am not sure whether the current results can be treated as up-to-date findings. Third, the methods are idiosyncratic in that the main manipulation took place only during the second reminder after the recruitment took place over mails and the letter reminder. To quote the authors, “More specifically, we introduce an email approach in the second of three reminders sent to non-responding physicians. In the first ten annual waves of the survey, the main mailout and all three reminders were delivered by mail only.” What was the reason that this specific mixed method was used for the study? Are there any empirical or theoretical basis to suggest that this method would be the best? In the discussion, the authors acknowledge these as potential limitations, and I think these limitations seriously compromise the generalizability of the findings. Fourth, it is unclear what the outcome measures; are they response rates only after the second reminder or after the first reminder? It sounds like it is the response rate regardless of the timepoint, and this can be an issue as noted in the next point. Fifth, the results reported in the abstract and as the main findings included data from two third of the participants in the intervention group who did not even receive the experimental treatment because they did not even have valid email addresses! These data should not even be reported. The authors also report results from those who had email addresses in both the intervention and control groups, and the response rates of both groups among these people are reduced from mid- to high thirty percent of the overall response rates down to low 20’s. Could it be the case that those who provided email addresses were more likely to have responded even before the manipulation? Other less major questions: Was the survey anonymous? If so, how was the online completion tracked in terms of which condition they belonged? If the survey responses had identifiers, couldn’t that be a factor that might compromise the generalizability of the findings? First sentence of Background; “Web surveys have lower response rates than other survey modes.” This is a strong statement and perhaps incorrect given the findings of the current study. Also, what are “other survey modes”? “…and this study also included nurses and physician assistants as well as physicians” This can sound somewhat politically incorrect as if nurses and physician assistants’ results are meaningless. Reviewer #2: The article provides an important contribution regarding surveys and data collection. It makes a good point, indicating that most of the studies in this area are ten years old and thus requires an update. It utilizes sound statistical methods and contributes to existing literature. Reviewer #3: Overall, the paper is well-structured, and the research question is clearly defined. The authors aim to compare the response rates between email and mailed approaches within a national longitudinal survey of physicians. I agree with the authors that this paper is up to date, considering that most studies in this area use data more than 10 years old, which justifies the need to re-examine this issue. The methods used in the study are robust and well-described, following the CONSORT guidelines and using appropriate statistical methods. The paper provides a clear comparison of response rates between the intervention and control groups, as well as subgroups of GPs and non-GP specialists. The results indicate that the response rate was lower for the email approach compared to the mailed approach. This difference was larger for GPs compared to non-GP specialists. In conclusion, the paper contributes valuable insights to the survey methods literature for physicians, particularly in the context of the increasing use of email and the internet in medical practice. The findings have practical implications for survey design and recruitment methods targeting physicians. Strengths: 1. The study followed the Consolidated Standards of Reporting Trials (CONSORT) guidelines, which ensures transparent and accurate reporting of the research process. 2. The research was conducted within the context of the Medicine in Australia: Balancing Employment and Life (MABEL) survey, a well-established longitudinal panel survey of all medical practitioners in Australia, providing a strong foundation for the study. 3. The sample frame for MABEL, the Medical Directory of Australia, is a national database of doctors, ensuring a comprehensive representation of the medical practitioner population. 4. The study used a randomized controlled trial with a parallel-arm design and 1:1 allocation, which allows for a rigorous comparison between the intervention and control groups. 5. The researchers employed stratified randomization to ensure that the proportions of different doctor types (GP, specialist), continuing or new, and boost sample in the intervention and control groups were the same. 6. The analysis was conducted by a researcher who was blinded to group allocation until after the analysis was complete and checked, reducing the risk of bias. Weaknesses: 1. The study relied on data from Wave 11, which was administered between August 2018 and April 2019, limiting the generalizability of the findings to more recent years. 2. The study excluded junior doctors, who might have different response rates and preferences compared to more experienced doctors, reducing the generalizability of the findings. 3. A significant proportion of the intervention group (43%) did not have an email address and were instead approached by mailed paper letter, which might underestimate the effect of the intervention for those who received an email. 4. The intervention only differed at the second reminder, which may not have been enough to fully capture the difference in response rates between email and mailed approaches. 5. The response rate differences between the intervention and control groups might be influenced by other factors not considered in the study, such as the timing of reminders and the content of the survey. Suggestions for improvement: 1. The authors could consider updating the study with more recent data to ensure the relevance of the findings to current survey methods and physician response rates. 2. To further assess the generalizability of the findings, the authors could include junior doctors in the sample (for future work) and analyze their response rates separately, providing insights into different age groups and experience levels. 3. The researchers could explore additional ways to improve email deliverability and reduce the proportion of participants without an email address to better assess the intervention's effectiveness. 4. The intervention could be extended to more than one reminder stage to better understand the cumulative effect of using email approaches over multiple reminders. 5. The authors could conduct sensitivity analyses to determine the impact of other factors, such as timing of reminders and survey content, on response rates in both intervention and control groups. This would provide a more comprehensive understanding of the factors influencing physician response rates. 6. Limited generalizability across different populations: The study was conducted exclusively within the Australian context, which may limit the generalizability of the findings to other countries with different healthcare systems, professional cultures, and survey response patterns. It would be beneficial to conduct similar studies in other countries to better understand how the intervention is performed in different settings. 7. Lack of examination of non-response bias: The study focused on response rates but did not explore potential non-response bias, which may arise if the doctors who chose to participate in the survey differ systematically from those who did not. It is important to investigate whether the intervention affected the composition of respondents in any way, as this may have implications for the interpretation of the survey results and their representativeness of the target population. 8. Limited exploration of factors influencing email effectiveness: The study did not investigate factors that could influence the effectiveness of email approaches, such as the timing of the email, subject lines, or the formatting of the email content. A more detailed investigation of these factors could help identify best practices for optimizing email reminders in future survey administration. 9. Single intervention approach: The study tested only one email-based intervention, which may not represent the full range of potential interventions that could be implemented to improve response rates. Future research could explore other interventions, such as varying the incentives for participation or using different communication channels, to determine the most effective strategies for increasing response rates. 10. No qualitative insights: The study did not provide any qualitative insights into the reasons behind the observed response rate differences between the intervention and control groups. Conducting interviews or focus groups with a subset of physicians could help researchers better understand the reasons for their survey participation preferences, which could inform future survey design and administration strategies. 11. Provide more information on the implications of their findings for healthcare and survey research communities. 12. Address the study's limitations in more detail and discuss potential ways to overcome them in future research. 13. Elaborate on the practical implications of their findings, such as cost savings, logistical benefits, and challenges or barriers to implementing email reminders. 14. Clearly outline the next steps needed for future research to build upon the current study and address its limitations. Writing Quality, Understanding Easiness, Clarity, and Organization: - Overall, the writing quality of the paper seems to be good, with clear descriptions of the methods, results, and conclusions. The organization appears logical, with sections following a conventional structure for a research article. - Suggestions for improvement: a) Some portions of the text, particularly in the Methods section, could be further clarified for better readability. Consider rephrasing complex sentences and providing more straightforward explanations of the study design and data analysis. b) In the Introduction and Discussion sections, the authors could provide more context on the importance of their research question and the implications of their findings for the broader healthcare and survey research communities. Content Accuracy, Comprehensiveness, Clinical Usefulness, and Significance: - The content appears accurate, and the methodology is comprehensive. However, some concerns have been raised regarding the study's limitations, which could impact the clinical usefulness and significance of the findings. - Suggestions for improvement: a) Address the weaknesses mentioned in previous comments, such as the limited generalizability of the study, potential non-response bias, and factors influencing email effectiveness. b) Explore additional intervention approaches, such as varying incentives for participation, using different communication channels, or incorporating personalized messaging to identify the most effective strategies for increasing response rates. c) Consider conducting a qualitative investigation to understand the reasons behind physicians' survey participation preferences, which could inform future survey design and administration strategies. d) Provide a more in-depth literature review to better contextualize the study within the broader research landscape and identify gaps in current knowledge. e) Discuss the practical implications of the study findings, including potential cost savings or logistical benefits of using email reminders, as well as any challenges or barriers to implementation. f) Include a more detailed description of the target population and the representativeness of the sample to help readers understand the context and relevance of the study findings. g) Present a clear plan for future research, outlining the next steps needed to build upon the current study and address its limitations. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: No Reviewer #3: No ********** [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. 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| Revision 1 |
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A randomised controlled trial of email versus mailed invitation letter in a national longitudinal survey of physicians. PONE-D-22-23734R1 Dear Dr. Scott, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Fares Alahdab, MD, MSc Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #3: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #3: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #3: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #3: No ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #3: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #3: Thank you for addressing my comments and revising your manuscript accordingly. I have no further comments to add. ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #3: No ********** |
| Formally Accepted |
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PONE-D-22-23734R1 A randomised controlled trial of email versus mailed invitation letter in a national longitudinal survey of physicians. Dear Dr. Scott: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Fares Alahdab Academic Editor PLOS ONE |
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