Peer Review History

Original SubmissionMarch 6, 2023
Decision Letter - Jerome Nyhalah Dinga, Editor

PONE-D-23-06419Longitudinal Assessment of COVID-19 Vaccine Uptake: A Two-Wave Survey of a Nationally Representative U.S. SamplePLOS ONE

Dear Dr. Katzman,

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.

Please submit your revised manuscript by Jul 06 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:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.
  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.
  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Jerome Nyhalah Dinga, PhD

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

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

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.

3. Thank you for stating the following financial disclosure:

“The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.” 

Please state what role the funders took in the study.  If the funders had no role, please state: "The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."

If this statement is not correct you must amend it as needed.

Please include this amended Role of Funder statement in your cover letter; we will change the online submission form on your behalf.

4. Thank you for stating the following in the Acknowledgments Section of your manuscript:

“Funding

The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.”

We note that you have provided funding information that is currently declared in your Funding Statement. However, funding information should not appear in the Acknowledgments section or other areas of your manuscript. We will only publish funding information present in the Funding Statement section of the online submission form.

Please remove any funding-related text from the manuscript and let us know how you would like to update your Funding Statement. Currently, your Funding Statement reads as follows:

“The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.” 

Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

5. Thank you for stating the following in the Competing Interests section:

“Caroline Katzman, Julen Harris, Christine Mauro, Ariel de Roche, and Tucker Morgan have no conflicts of interest to declare. Gregory Zimet serves as an external advisory board member for Pfizer and Moderna, and as a consultant to Merck. He also has received investigator-initiated research funding from Merck administered through Indiana University and serves as an unpaid member of the Board of Directors for the Unity Consortium, a non-profit organization that promotes adolescent health through vaccination. Susan Rosenthal has received investigator-initiated research funding from Merck Investigator Studies Program administered through Columbia University Irving Medical Center.”

Please confirm that this does not alter your adherence to all PLOS ONE policies on sharing data and materials, by including the following statement: "This does not alter our adherence to  PLOS ONE policies on sharing data and materials.” (as detailed online in our guide for authors http://journals.plos.org/plosone/s/competing-interests).  If there are restrictions on sharing of data and/or materials, please state these. Please note that we cannot proceed with consideration of your article until this information has been declared.

Please include your updated Competing Interests statement in your cover letter; we will change the online submission form on your behalf.

6. We note that you have stated that you will provide repository information for your data at acceptance. Should your manuscript be accepted for publication, we will hold it until you provide the relevant accession numbers or DOIs necessary to access your data. If you wish to make changes to your Data Availability statement, please describe these changes in your cover letter and we will update your Data Availability statement to reflect the information you provide.

7. Your ethics statement should only appear in the Methods section of your manuscript. If your ethics statement is written in any section besides the Methods, please move it to the Methods section and delete it from any other section. Please ensure that your ethics statement is included in your manuscript, as the ethics statement entered into the online submission form will not be published alongside your manuscript.

8. Please include a caption for figure 1.

9. Please include your tables as part of your main manuscript and remove the individual files. Please note that supplementary tables (should remain/ be uploaded) as separate "supporting information" files

[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

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: 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: Yes

**********

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

**********

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: This survey conducted in the United States adds to the evidence base concerning factors that drive one of the biggest global public health threats, i.e. vaccine hesitancy. Unfortunately, the study population was very small, resulting in highly imprecise estimates. Nonetheless, the study is interesting, and I especially enjoyed how the authors applied the “Diffusion of Innovation” model to how people behave with respect to COVID-19 vaccines.

That said, I believe the manuscript would benefit from revisions in order to more clearly and transparently describe various methodological aspects as well as the study findings. I hope my comments and suggestions below will help improve the paper.

ABSTRACT:

1. I strongly suggest briefly describing the study methods instead of jumping directly from rationale to results. In doing so, please make sure to clearly define the population of interest (adults? children? older adults? others?), indicate where the study was conducted, and describe participants’ selection methods (are these individuals meants to be representative of the general population?).

2. Please indicate the size the survey population and whether/how this changed from Wave 1 to Wave 2. It’s hard to interpret the study findings without any idea of how many people participated. Relatedly, I would suggest including 95% confidence intervals of prevalence proportions reported here.

INTRODUCTION:

1. As I am sure you know, COVID-19 is the disease caused by SARS-CoV-2, so the expression “COVID-19 infection” is not entirely correct and should be replaced with “SARS-CoV-2 infection”. Please revise the terminology throughout the manuscript to refer to COVID-19 or SARS-CoV-2 as appropriate.

2. Lines 64-66: I understand this may be intuitive, but I would suggest citing one or more references to support this statement.

3. Line 83: Consider adding the following citation along with references 2-5: Basta NE et al. Factors Associated With Willingness to Receive a COVID-19 Vaccine Among 23,819 Adults Aged 50 Years or Older: An Analysis of the Canadian Longitudinal Study on Aging. Am J Epidemiol. 2022 May 20;191(6):987-998. doi: 10.1093/aje/kwac029.

4. Lines 92-94: I would suggest rephrasing this sentence for clarity.

5. Lines 96-99: As also mentioned with respect to the abstract, I do think that the population and country of study should be clearly indicated. I encourage you to revise this last section of the introduction to incorporate this information. While some factors certainly play a role in favoring or hindering vaccine uptake across countries, other are more context specific. Given the peculiar social and political climate of the United States, I believe it is important to highlight the study context early on, as this also affects methodological choices as well as the interpretation of findings.

METHODS:

1. Consider slightly reorganizing the methods section into sub-sections with their own sub-headings to more systematically describe: the study design, cohort characteristics/sampling strategies, data collection methods, survey structure and relevant variables, and data analysis.

2. I am not familiar with this Ipsos panel, and it is unclear to me whether the survey was paper-based, by phone or online. Or perhaps multiple options were offered to participants to accommodate their needs and preferences?

3. What is the size of the Ipsos survey panel?

4. Considering that you leveraged on an existing survey panel, can you please clarify if the survey described in this article was developed ad hoc by the study authors or was part of a larger survey covering other health or social aspects?

5. If I understand correctly, Ipsos participants were invited to participate to your Waves 1 and 2 in addition to other surveys they were already involved in. Did you sample a subgroup of Ipsos participants or invited all of them to complete the questionnaire?

6. For clarity and transparency, it would be helpful to see the list of questions, response options along with the resulting variables and their categorization. For example, you mention gender, race/ethnicity, political views, and other variables, but we don’t know how this was categorized. I would suggest including this information in a supplementary file. However, I do think that some key details should be explained in-text. For example, the definition of “general vaccine attitudes” should be more clearly described considering that the study is focused around this concept. So, knowing which six questions were used to calculate this score is extremely important to the reader. Consider summarizing this information in a table.

7. Please clarify whether questionnaires administered at Wave 1 and Wave 2 include the exact same questions.

8. Please explain how missing data were handled.

9. How did you calculate weights?

10. How did you account for “variability introduced by subsampling”? Please expand the statistical analysis sub-section to provide some more details.

RESULTS:

1. As noted above, I think there is not enough clarity around the size of the study population. From Figure 1, we know that 1,189 people completed the Wave 1 survey and 843 completed the Wave 2 survey. It is still unclear what proportion of Ipsos participants were initially contacted and invited. Also, even if the numbers above are available in the flow diagram, I think it is important to include this information in-text as well, ideally in the Results’ opening sentence.

2. I am quite surprised to see that only regression analysis results are presented in the article. Please include descriptive statistics (table and text) before heading to the results to the logistic regression model.

3. Lines 162-164: I find this sentence quite confusing: “Briefly, of the 509 participants who were vaccinated at Wave 1 and returned for follow-up, all but 3 reported being vaccinated by Wave 2 (99%).” Is these people were vaccinated at Wave 1, what were they supposed to report at Wave 2? Did you ask them if they had received a second dose? Or just to confirm their vaccination status as reported at Wave 1? Please rephrase and clarify.

4. From the description of the results, I have trouble understanding whether there was any attempt to differentiate between first, second and booster doses. I believe this is an important point to discuss in the manuscript.

DISCUSSION:

1. I appreciate the discussion around the meaning and implications of the study findings. However, I strongly encourage you to revise it in order to incorporate considerations on whether and how your findings relate to other studies. What’s new in this study that was not captured in other studies? Do you think that your findings apply to other countries and why or why not? Also, what do your results tell us about attitudes towards vaccination in different parts of the US? I know the size of the study population was quite small and you certainly lacked power to conduct any subgroup analyses, but – in my opinion – this is an important point to discuss.

Reviewer #2: GENERAL COMMENTS TO AUTHORS

Overall this is a relatively well-designed and implemented study involving two KnowledgePanel surveys regarding COVID-19 vaccination intent and receipt- one fielded in April 2021 (when only some Americans were recommended to be vaccinated n the staged-in process due to vaccine supply) and the follow-up survey in February 2022 (when all Americans were vaccine-eligible). The study goal was to identify predictors of ultimate vaccination. The authors used a reasonable Diffusion of Innovation (DOI) conceptual model to ground their study and analysis. They found, unsurprisingly, that those who wanted the vaccine “ASAP” nearly all received it later, those who were cleary non-acceptors initially remained so afterwards, and those in between tended to be vaccinated with higher-income and barriers being moderate predictors in the wait-and-see group while belief structures were paramount in the non-acceptor group.

The study was done well, and the findings are believable. Key limitations are that Wave 1 occurred when some could get vaccinated so even the initial group was unusual (for example leaving out healthcare, essential workers, and older adults) from eligibility. Thus even prediction suffers from an unusual initial group. Second, sample sizes per DOI group were small (between 100-200 mostly), limiting confidence in prediction. Third, with the rapidly shifting background and concerns having to do with receipt of bivalent vaccine in a population which has largely already had COVID and largely already had at least 1 vaccination, the study implications at this point are limited.

SPECIFIC COMMENTS

Introduction

While well written, this section would be enhanced by relating the DOI and concepts to our current situation regarding COVID-19 vaccination and the likely future situation of having annual or biannual vaccine recommendations.

Methods

In general the methods were described well.

The authors could include a bit more on the underlying KnowledgePanel methods (recognizing that they published results of their original wave 1 study.

Results

The findings are presented relatively well and clearly

Discussion

This section is well thought out. It could be improved by increasing the discussion of study findings as it relates to the current situation of the US recommending bivalent vaccination for a population that has largely had COVID infection and has had at least one prior vaccination.

The discussion about relationship to influenza vaccination is not new and does not currently lend itself to actions. The authors should consider discussing how knowledge of influenza vaccination might practically help providers or health systems in their attempt to promote COVID-19 vaccination (beyond just showing the association). In addition, future COVID-19 vaccines might be combined with influenza vaccines so a discussion could cover that topic.

**********

[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/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Revision 1

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

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

We have edited this paper to fully reflect PLOS ONE’s style requirements including those for file naming.

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.

All participants in this study are members of the IPSOS KnowledgePanel®. Participants received an information sheet for this study which stated that completion of the questionnaire indicated consent to participate in this study. This has been added to the Methods and the Ethics Statement.

3. Thank you for stating the following financial disclosure:

“The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.”

Please state what role the funders took in the study. If the funders had no role, please state: "The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."

If this statement is not correct you must amend it as needed.

Please include this amended Role of Funder statement in your cover letter; we will change the online submission form on your behalf.

We have added this statement.

4. Thank you for stating the following in the Acknowledgments Section of your manuscript:

“Funding

The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.”

We note that you have provided funding information that is currently declared in your Funding Statement. However, funding information should not appear in the Acknowledgments section or other areas of your manuscript. We will only publish funding information present in the Funding Statement section of the online submission form.

Please remove any funding-related text from the manuscript and let us know how you would like to update your Funding Statement. Currently, your Funding Statement reads as follows:

“The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp.”

Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

We have removed this language from the manuscript and have included it within the cover letter. For the online submission form, the funding statement should read: “The study was supported in part by a research grant from Investigator-Initiated Studies Program of Merck Sharp & Dohme Corp grant awarded to Dr. Susan Rosenthal, Principal Investigator, and administered through Columbia University Irving Medical Center. The opinions expressed in this paper are those of the authors and do not necessarily represent those of Merck Sharp & Dohme Corp. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.”

5. Thank you for stating the following in the Competing Interests section:

“Caroline Katzman, Julen Harris, Christine Mauro, Ariel de Roche, and Tucker Morgan have no conflicts of interest to declare. Gregory Zimet serves as an external advisory board member for Pfizer and Moderna, and as a consultant to Merck. He also has received investigator-initiated research funding from Merck administered through Indiana University and serves as an unpaid member of the Board of Directors for the Unity Consortium, a non-profit organization that promotes adolescent health through vaccination. Susan Rosenthal has received investigator-initiated research funding from Merck Investigator Studies Program administered through Columbia University Irving Medical Center.”

Please confirm that this does not alter your adherence to all PLOS ONE policies on sharing data and materials, by including the following statement: "This does not alter our adherence to PLOS ONE policies on sharing data and materials.” (as detailed online in our guide for authors http://journals.plos.org/plosone/s/competing-interests). If there are restrictions on sharing of data and/or materials, please state these. Please note that we cannot proceed with consideration of your article until this information has been declared.

Please include your updated Competing Interests statement in your cover letter; we will change the online submission form on your behalf.

We have added this section, along with the statement above, to our Cover Letter. This section now reads: “Caroline Katzman, Julen Harris, Christine Mauro, Ariel de Roche, and Tucker Morgan have no conflicts of interest to declare. Gregory Zimet serves as an external advisory board member for Pfizer and Moderna, and as a consultant to Merck. He also has received investigator-initiated research funding from Merck administered through Indiana University and serves as an unpaid member of the Board of Directors for the Unity Consortium, a non-profit organization that promotes adolescent health through vaccination. Susan Rosenthal has received investigator-initiated research funding from Merck Investigator Studies Program administered through Columbia University Irving Medical Center. This does not alter our adherence to PLOS ONE policies on sharing data and materials.”

6. We note that you have stated that you will provide repository information for your data at acceptance. Should your manuscript be accepted for publication, we will hold it until you provide the relevant accession numbers or DOIs necessary to access your data. If you wish to make changes to your Data Availability statement, please describe these changes in your cover letter and we will update your Data Availability statement to reflect the information you provide.

All data necessary to replicate this study’s findings will be made available without restriction at data repository ICPSR.

7. Your ethics statement should only appear in the Methods section of your manuscript. If your ethics statement is written in any section besides the Methods, please move it to the Methods section and delete it from any other section. Please ensure that your ethics statement is included in your manuscript, as the ethics statement entered into the online submission form will not be published alongside your manuscript.

The Ethics Statement was moved to the Methods section of the paper. The Institutional Review Board of Columbia University Irving Medical Center approved this study as an exempt protocol on December 22, 2020. (IRB-AAAT5154).

8. Please include a caption for figure 1.

The caption has been added.

9. Please include your tables as part of your main manuscript and remove the individual files. Please note that supplementary tables (should remain/ be uploaded) as separate "supporting information" files

The tables have been included in the manuscript. The supplemental tables will be uploaded as supporting information.

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: This survey conducted in the United States adds to the evidence base concerning factors that drive one of the biggest global public health threats, i.e. vaccine hesitancy. Unfortunately, the study population was very small, resulting in highly imprecise estimates. Nonetheless, the study is interesting, and I especially enjoyed how the authors applied the “Diffusion of Innovation” model to how people behave with respect to COVID-19 vaccines.

That said, I believe the manuscript would benefit from revisions in order to more clearly and transparently describe various methodological aspects as well as the study findings. I hope my comments and suggestions below will help improve the paper.

ABSTRACT:

1. I strongly suggest briefly describing the study methods instead of jumping directly from rationale to results. In doing so, please make sure to clearly define the population of interest (adults? children? older adults? others?), indicate where the study was conducted, and describe participants’ selection methods (are these individuals meants to be representative of the general population?).

We have added language about the study methods and included the above.

2. Please indicate the size the survey population and whether/how this changed from Wave 1 to Wave 2. It’s hard to interpret the study findings without any idea of how many people participated. Relatedly, I would suggest including 95% confidence intervals of prevalence proportions reported here.

We have added the population size in Waves 1 and 2 and have included 95% confidence intervals of prevalence proportions here.

INTRODUCTION:

1. As I am sure you know, COVID-19 is the disease caused by SARS-CoV-2, so the expression “COVID-19 infection” is not entirely correct and should be replaced with “SARS-CoV-2 infection”. Please revise the terminology throughout the manuscript to refer to COVID-19 or SARS-CoV-2 as appropriate.

Thank you for this point – this has been addressed throughout the manuscript.

2. Lines 64-66: I understand this may be intuitive, but I would suggest citing one or more references to support this statement.

We have added citations to support this.

3. Line 83: Consider adding the following citation along with references 2-5: Basta NE et al. Factors Associated With Willingness to Receive a COVID-19 Vaccine Among 23,819 Adults Aged 50 Years or Older: An Analysis of the Canadian Longitudinal Study on Aging. Am J Epidemiol. 2022 May 20;191(6):987-998. doi: 10.1093/aje/kwac029.

Thank you for sharing this resource! We have included it in the manuscript.

4. Lines 92-94: I would suggest rephrasing this sentence for clarity.

This line has been rephrased.

5. Lines 96-99: As also mentioned with respect to the abstract, I do think that the population and country of study should be clearly indicated. I encourage you to revise this last section of the introduction to incorporate this information. While some factors certainly play a role in favoring or hindering vaccine uptake across countries, other are more context specific. Given the peculiar social and political climate of the United States, I believe it is important to highlight the study context early on, as this also affects methodological choices as well as the interpretation of findings.

We have revised the introduction to include the country of study.

METHODS:

1. Consider slightly reorganizing the methods section into sub-sections with their own sub-headings to more systematically describe: the study design, cohort characteristics/sampling strategies, data collection methods, survey structure and relevant variables, and data analysis.

We have re-organized the Methods section into sub-sections for clarity.

2. I am not familiar with this Ipsos panel, and it is unclear to me whether the survey was paper-based, by phone or online. Or perhaps multiple options were offered to participants to accommodate their needs and preferences?

The survey is online only, we have included additional information about the Ipsos panel in the Methods section.

3. What is the size of the Ipsos survey panel?

The panel has 60,000 adult respondents, we have included this in the manuscript.

4. Considering that you leveraged on an existing survey panel, can you please clarify if the survey described in this article was developed ad hoc by the study authors or was part of a larger survey covering other health or social aspects?

The study authors developed the survey for this paper, we have included this in the manuscript.

5. If I understand correctly, Ipsos participants were invited to participate to your Waves 1 and 2 in addition to other surveys they were already involved in. Did you sample a subgroup of Ipsos participants or invited all of them to complete the questionnaire?

We sampled a subgroup of participants, we have included this and the exact numbers of panelists to the methods section of the manuscript.

6. For clarity and transparency, it would be helpful to see the list of questions, response options along with the resulting variables and their categorization. For example, you mention gender, race/ethnicity, political views, and other variables, but we don’t know how this was categorized. I would suggest including this information in a supplementary file. However, I do think that some key details should be explained in-text. For example, the definition of “general vaccine attitudes” should be more clearly described considering that the study is focused around this concept. So, knowing which six questions were used to calculate this score is extremely important to the reader. Consider summarizing this information in a table.

We have cited the group’s original paper which has a table with all questions from this survey and how the questions were scored. In addition, we have included examples of questions from each categories in-text for further clarity. Lastly, we have now included selected scaled questions from the Wave 1 Questionnaire used for this study in the Supporting Information files.

7. Please clarify whether questionnaires administered at Wave 1 and Wave 2 include the exact same questions.

Wave 1 and 2 surveys were near-identical, however the Wave 2 survey was updated to reflect the changes in COVID-19 vaccine policy and protocol (i.e. the vaccine was available to all participants at the time of the Wave 2 survey so a question about eligibility was updated). This has now been stated explicitly in the Methods section of the manuscript.

8. Please explain how missing data were handled.

There were three sources of missing data in this study. The first was missing data due to people being loss-to-follow-up between Wave 1 and Wave 2. The Wave 2 weights provided by IPSOS and used in these analyses were adjusted to account for this.

The second source of missing data were participants who did not complete the main item on vaccination in wave 2 (n=12). Since this was such a small percentage of the overall sample (< 3%), they were simply removed from the analysis. The last source of missing data was on individual covariates of interest. These individuals were simply removed from the bivariate analyses as needed and never exceeded four observations lost.

We have included this in the results section.

9. How did you calculate weights?

Ipsos calculated the weights for the findings to be nationally representative, and these values were used for the analysis. We have added more detail about the Ipsos’ methodology for calculating weights in the Methods section.

RESULTS:

1. As noted above, I think there is not enough clarity around the size of the study population. From Figure 1, we know that 1,189 people completed the Wave 1 survey and 843 completed the Wave 2 survey. It is still unclear what proportion of Ipsos participants were initially contacted and invited. Also, even if the numbers above are available in the flow diagram, I think it is important to include this information in-text as well, ideally in the Results’ opening sentence.

1991 participants were invited to “Wave 1” and 1062 participants were invited to “Wave 2,” this has been included in the first line of the Results section.

2. I am quite surprised to see that only regression analysis results are presented in the article. Please include descriptive statistics (table and text) before heading to the results to the logistic regression model.

We have added a new table with descriptive statistics for the entire sample. We have also added a section in the Results that lays out the findings presented in this table.

3. Lines 162-164: I find this sentence quite confusing: “Briefly, of the 509 participants who were vaccinated at Wave 1 and returned for follow-up, all but 3 reported being vaccinated by Wave 2 (99%).” Is these people were vaccinated at Wave 1, what were they supposed to report at Wave 2? Did you ask them if they had received a second dose? Or just to confirm their vaccination status as reported at Wave 1? Please rephrase and clarify.

We added language to state that this is likely due to participant error (these three participants reported vaccination initially and then stated they had not been vaccinated later).

4. From the description of the results, I have trouble understanding whether there was any attempt to differentiate between first, second and booster doses. I believe this is an important point to discuss in the manuscript.

We added a sentence in the Methods section clarifying that we asked how many doses were received (only 2 doses were available at the time of the survey). However, for this analysis, we considered “vaccinated” as having received one vaccine dose. This is also discussed further in the limitations section of the paper.

DISCUSSION:

1. I appreciate the discussion around the meaning and implications of the study findings. However, I strongly encourage you to revise it in order to incorporate considerations on whether and how your findings relate to other studies. What’s new in this study that was not captured in other studies?

We have been more explicit in the Discussion about the ways in which our findings contribute to the literature, both in novel and in supportive ways.

Do you think that your findings apply to other countries and why or why not? Also, what do your results tell us about attitudes towards vaccination in different parts of the US?

Our data likely does not apply to other countries or various regions of the U.S. based on specific social/political contexts and vaccine availability. Additionally, this study was designed to be nationally representative but not regionally representative and thus cannot answer the question of attitudes toward vaccination in different parts of the US. We have added this to the “Limitations” section of the discussion.

I know the size of the study population was quite small and you certainly lacked power to conduct any subgroup analyses, but – in my opinion – this is an important point to discuss.

Thank you for this point – we have added this to the limitations section.

Reviewer #2: GENERAL COMMENTS TO AUTHORS

Overall this is a relatively well-designed and implemented study involving two KnowledgePanel surveys regarding COVID-19 vaccination intent and receipt- one fielded in April 2021 (when only some Americans were recommended to be vaccinated n the staged-in process due to vaccine supply) and the follow-up survey in February 2022 (when all Americans were vaccine-eligible). The study goal was to identify predictors of ultimate vaccination. The authors used a reasonable Diffusion of Innovation (DOI) conceptual model to ground their study and analysis. They found, unsurprisingly, that those who wanted the vaccine “ASAP” nearly all received it later, those who were cleary non-acceptors initially remained so afterwards, and those in between tended to be vaccinated with higher-income and barriers being moderate predictors in the wait-and-see group while belief structures were paramount in the non-acceptor group.

The study was done well, and the findings are believable. Key limitations are that Wave 1 occurred when some could get vaccinated so even the initial group was unusual (for example leaving out healthcare, essential workers, and older adults) from eligibility. Thus even prediction suffers from an unusual initial group. Second, sample sizes per DOI group were small (between 100-200 mostly), limiting confidence in prediction. Third, with the rapidly shifting background and concerns having to do with receipt of bivalent vaccine in a population which has largely already had COVID and largely already had at least 1 vaccination, the study implications at this point are limited.

SPECIFIC COMMENTS

Introduction

While well written, this section would be enhanced by relating the DOI and concepts to our current situation regarding COVID-19 vaccination and the likely future situation of having annual or biannual vaccine recommendations.

This is a great point. The importance of this data for future recommendations about bivalent boosters and annual/biannual vaccination was included to the introduction.

Methods

In general the methods were described well.

The authors could include a bit more on the underlying KnowledgePanel methods (recognizing that they published results of their original wave 1 study.

More information about the KnowledgePanel was included in this draft of the manuscript.

Results

The findings are presented relatively well and clearly

Thank you for this feedback!

Discussion

This section is well thought out. It could be improved by increasing the discussion of study findings as it relates to the current situation of the US recommending bivalent vaccination for a population that has largely had COVID infection and has had at least one prior vaccination.

Thank you for this point – we have added a section about the evolving landscape of COVID-19 vaccination and the continued importance of these findings.

The discussion about relationship to influenza vaccination is not new and does not currently lend itself to actions. The authors should consider discussing how knowledge of influenza vaccination might practically help providers or health systems in their attempt to promote COVID-19 vaccination (beyond just showing the association). In addition, future COVID-19 vaccines might be combined with influenza vaccines so a discussion could cover that topic.

Thank you for this – we have added this important point to the discussion.

Attachments
Attachment
Submitted filename: COVIDVaxResponsetoReviewersv2.docx
Decision Letter - Jerome Nyhalah Dinga, Editor

Longitudinal assessment of COVID-19 vaccine uptake: A two-wave survey of a nationally representative U.S. sample

PONE-D-23-06419R1

Dear Dr. Katzman,

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,

Jerome Nyhalah Dinga, PhD

Academic Editor

PLOS

Formally Accepted
Acceptance Letter - Jerome Nyhalah Dinga, Editor

PONE-D-23-06419R1

Longitudinal assessment of COVID-19 vaccine uptake: A two-wave survey of a nationally representative U.S. sample

Dear Dr. Katzman:

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. Jerome Nyhalah Dinga

Academic Editor

PLOS ONE

Open letter on the publication of peer review reports

PLOS recognizes the benefits of transparency in the peer review process. Therefore, we enable the publication of all of the content of peer review and author responses alongside final, published articles. Reviewers remain anonymous, unless they choose to reveal their names.

We encourage other journals to join us in this initiative. We hope that our action inspires the community, including researchers, research funders, and research institutions, to recognize the benefits of published peer review reports for all parts of the research system.

Learn more at ASAPbio .