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. 2024 Aug 22;19(8):e0309084. doi: 10.1371/journal.pone.0309084

Evaluating research ethics committees in Vietnam and Laos: Results of a validated self-assessment tool

Nathan Gabriel Sattah 1, Vincent D’Anniballe 1, Hoang Tu Le 2, Luyen Thi Le 3, Thanh Ngoc Le 3, Thom Thi Vu 3, Viengsakhone Louangpradith 4, Walter T Lee 5,*
Editor: Hadi Ghasemi6
PMCID: PMC11340885  PMID: 39172804

Abstract

Background

There is an increase in human subject research in developing countries and conducting them in an ethical manner depends on the research ethics oversight in these countries. The purpose of this study is to evaluate the operational, financial, and educational characteristics of research ethics committees (RECs) at institutions in Vietnam and Laos.

Methods

A validated self-assessment tool designed to assess nine major characteristics of RECs was translated into Vietnamese and Laotian. The translated surveys were delivered to and completed by representatives from RECs at institutions in Vietnam and Laos. The surveys were collected, translated back into English, and scored. The data was analyzed to identify potential areas of strength and areas for improvement.

Results

The mean survey score for the 19 RECs surveyed was 165.3 out of a maximum of 200 points with a standard deviation of 22.9. Committees scored the highest in the review of specific protocol items (95.6%), submission arrangements and materials (89.5%), and the policies referring to review procedures (85.6%) domains. RECs scored the lowest in the resources domain (65.5%), with only 26.3% of committees having an annual budget. Nearly all RECs have standard operating procedures (94.7%) and policies for disclosing conflicts of interest (89.5%). Most committees use prior ethics training as a criterion to select REC chairs (78.9%) and members (73.7%), with the majority of committees requiring a training course in ethics (76.5%). 68.4% of committees have continuing education in ethics for members and only 42.1% of committees have a budget for member training.

Conclusion

This study demonstrated that RECs in Vietnam and Laos have strong foundational review processes for research protocols. Important areas of improvement include improved institutional oversight, financial and administrative resources, and the continued ethics education for current committee members.

Introduction

The institutional review of new research protocols is an essential component of ethical medical research involving human subjects. Guidelines set forth by the Nuremberg Code, the Declaration of Helsinki, and the Good Clinical Practice guidelines establish ethical standards for institutional review boards (IRBs) and equivalent research ethics committees (RECs). These committees are responsible for the review and approval of study protocols, thereby maintaining research subject welfare and the scientific integrity of the research.

Despite these established frameworks, the steady increase in clinical research involving human subjects in low- or middle-income countries (LMICs), especially in Asia and the Middle East, raises questions about the capacity for ethics oversight in these nations [14]. Indeed, studies examining ethics committees in the Eastern Mediterranean and Middle East found that members lacked formal ethics training, that committees had limited financial and administrative resources, and that there is a need for greater diversity within committees [5, 6]. Improved training on research ethics is also needed in LMICs, as demonstrated by one study showing inadequate experience in data sharing and knowledge of data ethics and legislation in Sub-Saharan Africa [7]. These findings suggest opportunities for improvement in the ethical review infrastructure, which may be prevalent across developing nations.

This study’s overall aim was to assess the organizational, logistical, educational, and financial characteristics of RECs in Vietnam and Laos. These two countries are geographical neighbors and share many cultural and political parallels, therefore their understanding and implementation of RECs may be similar. In Vietnam, the Ministry of Health oversees clinical trials and research organizations, such as institutional RECs, that perform research studies [8]. Despite this national oversight, cultural factors such as language and lower literacy rates may negatively influence participant perceptions of research ethics in Vietnam [9]. In Laos, research undertaken by institutions has little national oversight and is often funded by outside donors [10]. These ethical challenges raise important concerns regarding the operations of RECs in Vietnam and Laos.

To date, this will be the first study to evaluate the RECs of institutions in Vietnam and Laos. By surveying institutions in these countries, this study hopes to identify areas of strength and areas for potential improvement in the ethical review process. The results of this study will not only advance ethical oversight at these institutions, but also will contribute to a wider dialogue about strategies to improve the quality of research ethics review in LMICs.

Materials and methods

Study recruitment

This study was deemed exempt by the institutional review board (S1 File). A convenience sample of institutions in Vietnam and Laos were selected based upon established collaborations with the Vietnam National University–University of Medicine and Pharmacy and with the Laos Ministry of Health. These institutions oversee several hospital systems in their respective countries and aided in the recruitment for this study. Inclusion criteria for selected institutions were current or historical participation in human subject research activity and a willingness to complete the REC survey. Institutions without current or any history of human subject research activity or an unwillingness to complete the survey were excluded from this study.

A total of 19 institutions, 17 in Vietnam and two in Laos, were recruited between August 1st 2023 and October 31st 2023. The following institutions from Vietnam were recruited: Hue Central Hospital, Can Tho University of Medicine and Pharmacy, Traditional Medicine Hospital, Hanoi Medical University, Hai Phong University of Medicine and Pharmacy, National Hospital of Dermatology and Venereology, Central Children’s Hospital, K Hospital, Thai Nguyen University of Medicine and Pharmacy, Hanoi Central Dental Hospital, Military Medical University, University of Public Health, Central Military Hospital 108, Hanoi National University–University of Medicine and Pharmacy, E Hospital, Lung Central Hospital, and Ho Chi Minh University of Medicine and Pharmacy. From Laos, the National Institute of Public Health and the University of Health Sciences of Lao participated in this study. Members of the RECs from all institutions received a description of the study by the study team and were provided the opportunity to ask questions. Verbal consent was obtained from REC members at each institution and documented by the study team before any study activities were conducted. Proceeding with the survey was contingent of verbal consent.

Survey selection and translation

Many existing REC self-assessment tools, such as those provided by the United States Office for Human Research Protections, the United Kingdom’s National Research Ethics Service, and the World Health Organization, lack the generalizability to LMICs and the comprehensiveness to include items relevant to REC functioning such as REC resources and process for informed consent and continuing review [4]. To evaluate the RECs in Vietnam and Laos, a validated and comprehensive self-assessment tool designed to evaluate RECs in developing nations created by Sleem et al. was used in this study (S2 File) [4].

This tool, originally written in English, was translated to ensure accessibility and comprehension by the target respondents. A professional translation service (Stepes) was employed to translate the questionnaire into certified Vietnamese and Laotian versions.

Survey distribution and collection

The translated surveys were distributed to the convenience sample of RECs. One member of the REC from each institution completed the survey. The process was facilitated through digital means, ensuring a broad reach and ease of participation for all involved institutions. The completed surveys in Vietnamese and Laotian were then translated back into English for scoring.

Scoring and data analysis

Surveys were scored based upon predefined criteria aligned with international ethical guidelines and best practices for RECs as outlined in Sleem et al [4]. Although the surveys were not anonymous, the data was de-identified for scoring. The maximum total score for the survey was 200 points and achieving a maximum score would indicate full compliance with international guidelines and standards for RECs. The survey is sub-divided into the nine following domains, each with their own sub-scores: organizational aspects (max 54 points), membership and educational training (max 30 points), submission arrangements and materials (max 12 points), minutes (max 13 points), policies referring to review procedures (max 11 points), review of specific protocol items (max 43 points), communicating a decision (max 5 points), continuing review (max 16 points), and REC resources (max 16 points).

The “organizational aspects” domain includes questions regarding the REC’s affiliation with and oversight by a governing institution, the presence of standard operating procedures, the policies and criteria for selecting members and chairs, and policies for disclosing conflicts of interest. The “membership and educational training” domain assesses the diversity of the committee and the methods of ethics training expected of committee members. The “submission arrangements and materials” domain evaluates the requirements needed for protocol submission including the use of templates, approval from the department chair, and deadlines for review. It also includes questions about the specific items which are required for protocol submission such as informed consent forms, investigator qualifications, and conflict of interest disclosures. The “minutes” domain determines whether committees maintain minutes of each meeting and evaluates the contents of such meeting minutes. The “policies referring to review procedures” domain includes questions about whether the REC has policies about how protocols will be reviewed, about the conditions for expedited review, and about how the interval of continuing review is determined. The “review of specific protocol items” domain is an in-depth assessment of the specific qualities of a protocol that are examined by the committee including, but not limited to, the risks of the protocol, the probable benefits of the research, the identification of vulnerable populations, the methods for maintaining confidentiality, and the elements of the informed consent. The “communicating a decision” domain assesses the approval letter sent to investigators in addition to the submission of amendments, adverse events, and protocol deviations. The “continuing review” domain queries the specific data that are requested during a continuing review report, such as the number of subjects withdrawn and any protocol violations or deviations. Lastly, the “REC resources” domain assesses whether the REC has an annual budget, access to physical resources like a meeting room, and the administrative staff available to the committee.

Analysis of the data included gathering means and standard deviations of total survey scores and individual domain scores. Furthermore, frequencies and percentages were also used to describe the contribution of each value in the variable. Statistical analysis of data between the two countries was performed using independent samples t-tests and revealed no statistically significant differences in total survey scores and domain scores at a significance level of α = 0.05, therefore our data are presented as one total cohort. Statistical analysis was conducted with Stata (version 18, Basic Edition).

The following general characteristics for analysis were used based on prior studies using this tool in other LMICs [11]. These characteristics were: duration of REC existence (intervals were chosen arbitrarily for this study), frequency of meetings, availability of an annual budget, and balanced gender representation [11].

Results

General characteristics of RECs

Survey responses were received from RECs at all 19 institutions. Raw, untranslated and scored survey responses may be found in S1S4 Datasets. The mean survey score for the cohort was 165.3 with a standard deviation of 22.9, corresponding to 82.7% of the maximum score. The median score was 169.

An evaluation of general characteristics of these institutions is shown in Table 1. We found that 52.6% of RECs have existed for more than 10 years. A distribution of the duration of existence and corresponding total survey score for all 19 RECs surveyed is shown in Fig 1. There was no correlation between the total score and the duration the REC has existed.

Table 1. General characteristics.

Number % Mean Survey Score (Maximum of 200) SD of Survey Scores
Duration of REC Existence
≤ 5 years 4 21.1 172.5 9.1
5–10 years 5 26.3 163.8 25.1
≥ 10 years 10 52.6 163.2 26.7
Frequency of Meetings
At least once a month 10 52.6 175.0 20.1
Less than once a month 9 47.4 154.6 21.9
Availability of an Annual Budget
Yes 5 26.3 182.8 12.6
No 14 73.7 159.1 22.8
Balanced Gender Representation1
Yes 2 11.1 177.0 7.1
No 16 88.9 164.4 24.5

1There was missing data from 1 institution about gender representation.

Fig 1. Distribution of duration of REC existence and total survey score.

Fig 1

Just over half of the committees meet at least once a month and around a quarter of committees reported having an annual budget. Additionally, RECs that meet at least once per month and that have an annual budget tended to score higher on the survey. Gender balance, defined as a female to male ratio between 0.4 and 0.6, was only achieved in two committees (11.1%).

Scores by survey domain

The mean score in each of the nine survey domains is shown in Table 2 as a percentage of the maximum score possible in the respective domain. The RECs scored the highest in the review of specific protocol items (95.6%) and the policies referring to review procedures (85.6%) domains, indicating a sufficiently thorough review process including assessments of potential risks and benefits, informed consents, and privacy measures. RECs also scored higher on the submission arrangements and materials domain (89.5%). Success in this domain demonstrates appropriate requirements for protocol submission and adequate support for submission such as guidelines, specific application forms, and templates.

Table 2. Scores by survey domain.

Mean Score (%) SD of Scores
Total Survey Score 82.7 22.9
Survey Domains
Review of Specific Protocol Items 95.6 3.4
Submission Arrangements and Materials 89.5 1.6
Policies Referring to Review Procedures 85.6 2.1
Communicating a Decision 83.2 1.5
Minutes 82.2 3.2
Continuing Review 81.9 5.2
Organizational Aspects 78.3 9.4
Membership and Educational Training 77.9 5.0
REC Resources 65.5 3.5

Although RECs scored on average less than 80% in the organizational aspects domain (78.3%), committees had several factors that indicated effective functioning. Most committees have written standard operating procedures (94.7%) and policies for disclosing conflicts of interest (89.5%). One important area of improvement in this domain was the regular evaluation of the REC by the governing institution, with 68.4% of RECs reporting such oversight.

The RECs surveyed scored the lowest in the resources domain (65.5%), indicating a clear need for both financial and administrative resources. As previously discussed, the presence of an annual budget is one area of improvement in this domain. Additionally, 12 committees (63.2%) reported that they do not have full time administrative staff.

The distribution of the scores in each domain is shown in Fig 2. This boxplot analysis reveals additional areas of strengths, with median scores of 100% in the communicating a decision and the continuing review domains. The communicating a decision domain assesses the approval letter sent to investigators in addition to the submission of amendments, adverse events, and protocol deviations. Favorable scores in the continuing review domain indicates a thorough evaluation of protocols over the course of the study. Additionally, the boxplot shows that there was missing data from some institutions on specific survey domains leading to domain scores of 0.

Fig 2. Boxplot of scores by survey domain.

Fig 2

Education and training for REC members

The analysis into the ethics background and training required of REC members revealed that committees readily use prior training in ethics and general research experience as criteria for selecting chairs and members (Table 3). However, only 2 institutions (10.5%) use prior publication specifically in the field of ethics to select the REC chair and only 1 institution (5.26%) use this criterion to select REC members. Other criterion given by respondents included a Good Clinical Practice training certification and subjective qualities such as the trust of the council, honesty, objectivity, and scientific reputation.

Table 3. Education and training across committees.

Number % of Committees
Criteria to Select Chair
Prior ethics training 15 78.9
Prior publication in ethics 2 10.5
Prior research experience 18 94.7
Other 5 26.3
Criteria to Select Members
Prior ethics training 14 73.7
Prior publication in ethics 1 5.3
Prior research experience 17 89.5
Other 6 31.6
Required Ethics Training for Membership1
Course 13 76.5
Web Training 3 17.6
Workshop 3 17.6
Other 3 17.6
Continuing Education in Ethics
Yes 13 68.4
Budget for Training
Yes 8 42.1
Established QI Program
Yes 8 42.1

Percentages do not add up to 100 because options are not mutually exclusive.

1There was missing data from 2 committees about required training for membership.

The specific medium of ethics training required for committee membership consisted primarily of a training course (76.5%). Fewer committees require web training or a workshop on ethics. The only other response provided was a certification of completion of the Good Clinical Practice training. As for current REC members, only 68.4% of committees require continuing education in research ethics for their members. One reason for the lack of continued education among some RECs may be that less than half of committees (42.1%) have a formal budget for the training of their members.

For RECs, quality improvement (QI) initiatives are foundational for the continued self-assessment and growth of both logistical processes and ethical standards. Eight institutions (42.1%) were found to have established QI programs. Financial and labor resources are likely the major barrier for institutions without a QI program.

Discussion

In summary, this study demonstrates the first evaluation RECs in Vietnam and Laos. The results of a validated survey administered to 19 institutions revealed that RECs in these countries demonstrated adequate review of research protocols and requirements for protocol submission.

Recognizing that the function of RECs is multifactorial, the survey data reports that standard operating procedures and infrastructure for declaring conflicts of interests are present.

This study also identified resources as the main area of improvement. Based upon survey responses, the establishment of a formal annual budget and the earmarking of funds for member ethics training should be discussed. Establishing regular oversight by the governing institution may be a method for securing additional funding and administrative resources [12].

From an ethics training and education standpoint, this study found that RECs appropriately used prior ethics training such as a training course and prior research experience as criteria to select committee chairs and members. To further bolster the ethics background of members and to facilitate robust ethics discussions, committees might consider requiring or screening for prior ethics publications in potential REC chairs and members [13]. Furthermore, this study showed that the development of QI programs aimed at evaluating internal ethical standards and a greater focus on the continued ethics education of members should be considered, as funds permit. This could include bioethical training programs that involve both graduate and post-graduate educational opportunities [14].

The challenges that the RECs in this study faced are not uncommon to those faced by RECs in other LMICs. Studies have shown that RECs in the Middle East and Africa have limited funding and limited ethics training for REC members and have demonstrated membership composition and training as key areas for improvement [6, 11, 15]. Indeed, studies have used the same validated survey to evaluate the RECs in these countries and in other South Asian countries like India and Myanmar [11, 16]. While the committees in Vietnam and Laos performed better on this specific self-assessment when compared to RECs in these regions, future work involving more rigorous statistical analysis is required to compare the validated survey results from the RECs of these countries.

Literature on the ethics teaching infrastructure in Northern Africa and some countries in the Middle East have revealed a scarcity of formal ethics education infrastructure, with many countries instead leaning on a select few pioneers for ethics teaching [17]. Indeed, authors have called for institutional and national support in developing nationally accredited programs to teach medical and research ethics at multiple levels of education within these nations [7, 1719]. This study did not elucidate the educational capacity of Vietnam and Laos for ethics at the undergraduate or graduate levels. However, future work should assess this capacity to ensure that sound ethics principles are not only taught to future researchers from an early stage of medical training, but also to current practicing health professionals.

There are several limitations to this study. This study used a convenience sample of RECs, and the results of the survey may be affected by recall and response bias. Additionally, cultural and language differences may have impacted how survey questions were interpreted. This was addressed by using certified translation software to mitigate language barriers. Lastly, the sample size was limited for RECs in Laos since that is what is currently active, which impeded the ability to delineate differences in RECs between these two countries.

In conclusion, this is the first study examining the current state RECs in medical research institutions in Vietnam and Laos. A survey administered to RECs demonstrated adequate foundational review processes, protocol submission policies, continuing protocol review, and communicating a decision about protocol approval. Potential areas of improvement included financial support, budget formation, and administrative labor. More continuing ethics training is needed for REC members and additional ethics training should be considered at the pre- and post-graduate levels.

Supporting information

S1 File. Institutional review board outcome letter.

(PDF)

pone.0309084.s001.pdf (70.8KB, pdf)
S2 File. Research Ethics Committee (REC) quality assurance self-assessment tool.

(PDF)

pone.0309084.s002.pdf (12.2MB, pdf)
S1 Dataset. Scored survey responses.

(XLSX)

pone.0309084.s003.xlsx (30.1KB, xlsx)
S2 Dataset. Raw, untranslated Vietnam survey responses.

(XLSX)

pone.0309084.s004.xlsx (28.6KB, xlsx)
S3 Dataset. Raw, untranslated Laos institution 1 survey response.

(DOCX)

pone.0309084.s005.docx (31.7KB, docx)
S4 Dataset. Raw, untranslated Laos institution 2 survey response.

(DOCX)

pone.0309084.s006.docx (32.1KB, docx)

Acknowledgments

We would like to acknowledge the REC leaders from the 17 Vietnam institutions and the two Laos institutions that provided the survey responses and data. We also acknowledge the support of Madame Lien Tran.

Data Availability

All relevant data are within the manuscript and its Supporting information files.

Funding Statement

The author(s) received no specific funding for this work.

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PONE-D-24-13355Evaluating Research Ethics Committees in Vietnam and Laos: Results of a Validated Self-Assessment ToolPLOS ONE

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Reviewer #2: 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: No

**********

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: Thank you for the opportunity to review the article. The paper covers an important topic. However, I would like to raise a few points that I think the authors should consider to make the article more readable. These comments are intended to increase the transparency of the description without detracting from the scientific value.

1. It is worth adding (e.g. as supplementary material) the form used to evaluate the performance of research ethics committees. The authors indicate that the base reference is an article by Sleem (2010) but adding a direct form that was used will increase the readability of the article.

2. I would like to ask the authors to add additional explanations on how the institutions and their representatives were selected and who was responsible for conducting the evaluation. What were the criteria for inclusion and exclusion of institutions? Please specify what is meant by the term "potential representatives".

3. Does the study have a research protocol, and if so, has it had prior registration?

4. In the description of the methods, the authors mention that the maximum possible score is 200. However, it is not clear what this means. Since in results the number of points obtained is a key part, it is necessary to add an explanation of what this means. Please enrich the manuscript with more data on the tool used.

5. line 117-119 p. 4: The article should describe in detail how the statistical analysis was carried out - what statistical methods were used for comparison.

6. line 121-122 p.4: “The following general characteristics for analysis were used based on prior studies using this tool in other LMICs.” Citations needed.

7. Data are presented at the research ethics committee level. However, the number of respondents within each committee is not reported. Was one representative selected within each institution?

8. Data on what the responses to each question were within the domains of the survey should also be included in the manuscript (or in supplementary material). In addition, it would be useful to give a more detailed explanation of what each domain means.

9. It is not clear if the survey was anonymous. I can't find any information about the institutions that participated in the survey, does this mean that the data was not collected?

10. The conclusions presented in lines 212-217 (page 8) seem too far-fetched. Does the existence of standard operating procedures and infrastructure for declaring conflicts of interest mean effective operation? In this situation, it is only a premise, as we do not know how it is used in practice. Correction of that sentences is needed. In excerpts on lines 212-233 on page no. 8, additional references should be inserted to support the authors' statements.

Reviewer #2: The article under review addresses a compelling subject matter. Nonetheless, the methodology employed suffers from deficiencies, primarily characterized by inadequate description and a conspicuous absence of essential procedural information pertaining to the research's execution.

Foremost among these deficiencies is the discrepancy between the authors' assertion that the research excludes human subjects and the evident utilization of a survey method involving representatives from 19 institutions, whose input in the form of opinions/data, and verbal consent was solicited. This incongruity raises ethical concerns regarding the absence of documented ethical clearance or ethical review for the study.

Moreover, the opacity surrounding the number of subjects interviewed, coupled with the absence of the questionnaire (at least in the English version) and an adequate description exposition of the tool employed, renders the methodology incompletely documented. Likewise, insufficient elucidation of the translation and adaptation process exacerbates the methodological ambiguity.

Lastly, the conclusions drawn in the article appear unsubstantiated by the evidence presented. For instance, the extrapolation of 'effective functioning' solely from the mere presence of standard operating procedures and infrastructure for declaring conflicts of interest seems unwarranted.

In light of these methodological shortcomings, the article lacks the requisite standard for publication.

**********

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

**********

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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.

PLoS One. 2024 Aug 22;19(8):e0309084. doi: 10.1371/journal.pone.0309084.r002

Author response to Decision Letter 0


22 Jun 2024

We thank the reviewers for recognizing our work to be an “important topic”

“compelling subject matter” and “scientific value”. Below is the point-by-point response to the valuable comments. Thank you for helping us improve our report.

Reviewer 1:

1. It is worth adding (e.g. as supplementary material) the form used to evaluate the performance of research ethics committees. The authors indicate that the base reference is an article by Sleem (2010) but adding a direct form that was used will increase the readability of the article.

A copy of the survey created by Sleem et al. and used in this study has been added to the supplementary materials.

2. I would like to ask the authors to add additional explanations on how the institutions and their representatives were selected and who was responsible for conducting the evaluation. What were the criteria for inclusion and exclusion of institutions? Please specify what is meant by the term "potential representatives".

We have clarified that this study is based upon a convenience sample of institutions and that the Vietnam National University – University of Medicine and Pharmacy and the Laos Ministry of Health aided us in the recruitment of the participating institutions (lines 82 - 87). This has also been added as a limitation to this study (line 297). Of note there are only 2 review boards in Laos and both did participate.

We have clarified the inclusion criteria (line 86).

We have clarified that specifically members of the REC at each institution agreed to participate in the study and filled out the survey (line 98, line 100, line 114)

3. Does the study have a research protocol, and if so, has it had prior registration?

This study was deemed exempt by our institutions institutional review board. Our outcome letter has been provided with our submission.

4. In the description of the methods, the authors mention that the maximum possible score is 200. However, it is not clear what this means. Since in results the number of points obtained is a key part, it is necessary to add an explanation of what this means. Please enrich the manuscript with more data on the tool used.

This study utilized a survey created by Sleem et al. (as referenced in the manuscript) which indicates that the survey design was based upon internal guidelines and standards for RECs. An explanation regarding the maximum score was added to line 124.

5. line 117-119 p. 4: The article should describe in detail how the statistical analysis was carried out - what statistical methods were used for comparison.

A more detailed explanation of the statistical methods, including statistical test and software employed, has been added to lines 156 – 162.

6. line 121-122 p.4: “The following general characteristics for analysis were used based on prior studies using this tool in other LMICs.” Citations needed.

A citation has been added to this sentence on line 165.

7. Data are presented at the research ethics committee level. However, the number of respondents within each committee is not reported. Was one representative selected within each institution?

It has been specified that one REC member from each institution completed the survey (line 114).

8. Data on what the responses to each question were within the domains of the survey should also be included in the manuscript (or in supplementary material). In addition, it would be useful to give a more detailed explanation of what each domain means.

Our raw, untranslated and scored survey responses have been provided as supplementary material.

Furthermore, a paragraph detailing the contents of each survey domain has been provided on lines 132 - 154.

9. It is not clear if the survey was anonymous. I can't find any information about the institutions that participated in the survey, does this mean that the data was not collected?

The survey was not anonymous, although the institutions were deidentified during analysis. This clarification has been added to line 124.

The names of the institutions that participated in this study has been added to lines 90 - 98.

10. The conclusions presented in lines 212-217 (page 8) seem too far-fetched. Does the existence of standard operating procedures and infrastructure for declaring conflicts of interest mean effective operation? In this situation, it is only a premise, as we do not know how it is used in practice. Correction of that sentences is needed. In excerpts on lines 212-233 on page no. 8, additional references should be inserted to support the authors' statements.

We have modified our statements in lines 258 - 260 and line 304 to more appropriately characterize our findings.

References have been added to lines 265, 271, 276 to bolster some of the suggestions made.

Reviewer 2:

The absence of documented ethical clearance or ethical review for the study.

As clarified in line 82 and as demonstrated by the outcome letter included in our submission, this study was deemed exempt by the institutional review board at our institution.

Moreover, the opacity surrounding the number of subjects interviewed, coupled with the absence of the questionnaire (at least in the English version) and an adequate description exposition of the tool employed, renders the methodology incompletely documented. Likewise, insufficient elucidation of the translation and adaptation process exacerbates the methodological ambiguity.

A copy of the survey created by Sleem et al. and used in this study has been added to the supplementary materials.

As stated in our methods section, an authorized translation service called Stepes was utilized to translate the survey in Vietnamese and Laotian. The certifications for this translation have been included in our supplemental materials. Furthermore, these methods were reviewed by the institutional review board at our institution.

Lastly, the conclusions drawn in the article appear unsubstantiated by the evidence presented. For instance, the extrapolation of 'effective functioning' solely from the mere presence of standard operating procedures and infrastructure for declaring conflicts of interest seems unwarranted.

We have modified our statements in lines 258 - 260 and 304 to more appropriately characterize our findings.

Attachment

Submitted filename: 1. Reviewer Comments WTL.docx

pone.0309084.s007.docx (19.6KB, docx)

Decision Letter 1

Hadi Ghasemi

23 Jul 2024

PONE-D-24-13355R1Evaluating Research Ethics Committees in Vietnam and Laos: Results of a Validated Self-Assessment ToolPLOS ONE

Dear Dr.  Lee, 

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 Sep 06 2024 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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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,

Hadi Ghasemi

Academic Editor

PLOS ONE

[Note: HTML markup is below. Please do not edit.]

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 #1: All comments have been addressed

Reviewer #3: (No Response)

Reviewer #4: 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 #1: Yes

Reviewer #3: No

Reviewer #4: Partly

**********

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

Reviewer #1: Yes

Reviewer #3: I Don't Know

Reviewer #4: 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 #1: Yes

Reviewer #3: Yes

Reviewer #4: Yes

**********

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 #1: Yes

Reviewer #3: (No Response)

Reviewer #4: 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 #1: Dear Authors,

Thank you for referring to my comments and making changes in the manuscript.

One additional request: Please include a reference to the Supplementary Materials in the manuscript text.

I recommend acceptance of the paper.

Reviewer #3: The background section lacks enough content on the status of RECs in the two countries, other the LMICs and various tools available for evaluation of RECs.

Reviewer #4: Thank you for your revised and interesting manuscript. Significant improvements have been made based on the initial feedback, but there are still some areas that from my point of view, require further attention to ensure the manuscript meets the highest standards:

1- The inclusion and exclusion criteria in methodology needs further elaboration. Line 86: "active involvement" seems to be an inclusion criterion; however, it would be better if you could point out what that concretely means. Try to name your exclusion criteria, if any, to strengthen the section.

2- Line 259, 260: Assessing the functionality of RECs based solely on the infrastructures or the standard operations is not unfortunately possible. Other factors such as REC members' experience or skills may play vital roles.

2- The comparisons with RECs in the Middle East, Africa, and South Asia at discussion are insightful, but they require more detailed data to be fully convincing. While relevant studies have been cited and provided survey data, adding specific performance metrics and more detailed statistical comparisons would strengthen these sections. (Statistically, if you want to justify that a country performed better, you cannot just compare the scores.)

3- Most of the references are older than 5 years. It would be great if you could check and add newer references.

Thank you for your hard work on this important study.

**********

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 #1: No

Reviewer #3: No

Reviewer #4: 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/. 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.

PLoS One. 2024 Aug 22;19(8):e0309084. doi: 10.1371/journal.pone.0309084.r004

Author response to Decision Letter 1


31 Jul 2024

We are pleased that some of the reviewers recognize the value of thus work for publication. We thank the journal for the opportunity to make it stronger based on the comments below

PLOS ONE Reviewer Comments

Reviewer 1:

1. Dear Authors,

Thank you for referring to my comments and making changes in the manuscript. One additional request: Please include a reference to the Supplementary Materials in the manuscript text. I recommend acceptance of the paper.

References to the Supplementary Materials have been added to lines 89, 121, and 189. Additionally, a “Supporting Information” section has been added to the end of the manuscript detailing the supporting information with captions.

Reviewer 3:

The background section lacks enough content on the status of RECs in the two countries, other the LMICs and various tools available for evaluation of RECs.

Peer-reviewed literature about research ethics in Vietnam and Laos are sparse. Some information regarding the oversight of clinical research in each country has been added to lines 72 - 77. As stated in line 79, this is the first study characterizing the RECs in Vietnam and Laos.

An extra source on RECs in other LMICs was added to lines 63 - 66 to highlight opportunities for improvements in training/education of research ethics.

A sentence explaining our choice of survey for this study was added to the Methods in lines 115 - 119.

Reviewer 4:

1. The inclusion and exclusion criteria in methodology needs further elaboration. Line 86: "active involvement" seems to be an inclusion criterion; however, it would be better if you could point out what that concretely means. Try to name your exclusion criteria, if any, to strengthen the section.

More precise inclusion and exclusion criteria have been added to lines 93 - 96.

2. Line 259, 260: Assessing the functionality of RECs based solely on the infrastructures or the standard operations is not unfortunately possible. Other factors such as REC members' experience or skills may play vital roles.

This sentence has been modified to take this comment into account in lines 275 - 276.

3. The comparisons with RECs in the Middle East, Africa, and South Asia at discussion are insightful, but they require more detailed data to be fully convincing. While relevant studies have been cited and provided survey data, adding specific performance metrics and more detailed statistical comparisons would strengthen these sections. (Statistically, if you want to justify that a country performed better, you cannot just compare the scores.)

While statistical analysis to compare the validated survey results was not performed in this study, the discussion of the literature on this topic has been modified based on these comments in lines 296 - 301.

4. Most of the references are older than 5 years. It would be great if you could check and add newer references.

5 additional references published within the last 5 years were added while addressing all reviewer comments.

Attachment

Submitted filename: 1. Response to Reviewers.docx

pone.0309084.s008.docx (17.9KB, docx)

Decision Letter 2

Hadi Ghasemi

6 Aug 2024

Evaluating Research Ethics Committees in Vietnam and Laos: Results of a Validated Self-Assessment Tool

PONE-D-24-13355R2

Dear Dr. Lee,

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 will be generated when your article is formally accepted. Please note, if your institution has a publishing partnership with PLOS and your article meets the relevant criteria, all or part of your publication costs will be covered. Please make sure your user information is up-to-date by logging into Editorial Manager at Editorial Manager® and clicking the ‘Update My Information' link at the top of the page. If you have any questions relating to publication charges, 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,

Hadi Ghasemi

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 #4: 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 #4: Yes

**********

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

Reviewer #4: 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 #4: Yes

**********

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 #4: 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 #4: Thank you for considering my comments and revising the manuscript accordingly.

For more clarity, you could also change Line 95 "Institutions without current or any history..." to "Institutions without current or past human subject research activity, or those unwilling to complete the survey, were excluded from this study."

**********

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 #4: No

**********

Acceptance letter

Hadi Ghasemi

12 Aug 2024

PONE-D-24-13355R2

PLOS ONE

Dear Dr. Lee,

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now being handed over to our production team.

At this stage, our production department will prepare your paper for publication. This includes ensuring the following:

* All references, tables, and figures are properly cited

* All relevant supporting information is included in the manuscript submission,

* There are no issues that prevent the paper from being properly typeset

If revisions are needed, the production department will contact you directly to resolve them. If no revisions are needed, you will receive an email when the publication date has been set. At this time, we do not offer pre-publication proofs to authors during production of the accepted work. Please keep in mind that we are working through a large volume of accepted articles, so please give us a few weeks to review your paper and let you know the next and final steps.

Lastly, 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 customercare@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. Hadi Ghasemi

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 File. Institutional review board outcome letter.

    (PDF)

    pone.0309084.s001.pdf (70.8KB, pdf)
    S2 File. Research Ethics Committee (REC) quality assurance self-assessment tool.

    (PDF)

    pone.0309084.s002.pdf (12.2MB, pdf)
    S1 Dataset. Scored survey responses.

    (XLSX)

    pone.0309084.s003.xlsx (30.1KB, xlsx)
    S2 Dataset. Raw, untranslated Vietnam survey responses.

    (XLSX)

    pone.0309084.s004.xlsx (28.6KB, xlsx)
    S3 Dataset. Raw, untranslated Laos institution 1 survey response.

    (DOCX)

    pone.0309084.s005.docx (31.7KB, docx)
    S4 Dataset. Raw, untranslated Laos institution 2 survey response.

    (DOCX)

    pone.0309084.s006.docx (32.1KB, docx)
    Attachment

    Submitted filename: 1. Reviewer Comments WTL.docx

    pone.0309084.s007.docx (19.6KB, docx)
    Attachment

    Submitted filename: 1. Response to Reviewers.docx

    pone.0309084.s008.docx (17.9KB, docx)

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting information files.


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