Difference between revisions of "Protecting Human Research Subjects"
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Research involving human subjects can pose complex [[Research Ethics | ethical]] issues that require careful thought and consideration on the part of both researchers and participants. Research teams must seek ethics certifications for human subjects approval to apply for and obtain [[IRB Approval | IRB approval]] and to protect the rights and welfare of study participants in a research project. This page will discuss the when, how, and who of ethics certifications for human research subjects. | Research involving human subjects can pose complex [[Research Ethics | ethical]] issues that require careful thought and consideration on the part of both researchers and participants. [[Impact Evaluation Team|Research teams]] must seek ethics certifications for human subjects approval to apply for and obtain [[IRB Approval | IRB approval]] and to protect the rights and welfare of study participants in a research project. This page will discuss the when, how, and who of '''ethics''' certifications for human research subjects. | ||
== Read First == | == Read First == | ||
*To protect the rights and welfare of study participants, [[IRB Approval | IRBs]] require ethics certifications; depending on IRB requirements, these may be obtained via NIH, CITI, or elsewhere. | * The [https://github.com/worldbank/dime-standards/tree/master/dime-research-standards/pillar-1-research-ethics DIME Research Ethics Standards] discuss the provisions for protecting human subjects in development research. | ||
* | * To protect the rights and welfare of study participants, [[IRB Approval | IRBs]] require '''ethics''' certifications; depending on '''IRB''' requirements, these may be obtained via NIH, CITI, or elsewhere. | ||
* Besides protecting human research subjects, the [[Impact Evaluation Team|research team]] must also keep in mind best practices for '''IRB approval''', [[Informed Consent|informed consent]], [[De-identification|de-identification]], and [[Encryption|encryption]]. | |||
== Overview == | == Overview == | ||
As a prerequisite for [[IRB Approval | IRB approval]], members of the research team who manage | As a prerequisite for [[IRB Approval | IRB approval]], all members of the [[Impact Evaluation Team|research team]] who manage [[Personally Identifiable Information (PII) | personally identifiable information (PII)]] must obtain '''ethics''' certifications to conduct research with human subjects. This may include principal investigators, research assistants, [[Field Coordinator|field coordinators]], and/or [[Survey Firm | survey firm]] staff. Two commonly accepted sources of certification are: | ||
* The | * The [https://phrptraining.com/ Protecting Human Research Participants Online Training] | ||
* The | * The [https://about.citiprogram.org/en/series/human-subjects-research-hsr/ Collaborative Institutional Training Initiative (CITI) Training] | ||
These courses cover the historical development of human subject protections, discuss the '''ethical''' issues involved in this human subjects research, and present the principles and regulations governing it. They are divided in modules that provide reading materials and entail quizzes for which a minimum score is required to pass each module. Learners may complete the modules at their own pace. | |||
== | Certificates usually have expirations and must be renewed. The CITI certificate must be renewed every 3 years, whereas the expiration of the NIH depends. Note that the '''IRBs''' can also define a date past which the certificates are considered invalid. | ||
== United States Standards == | |||
In the United States of America, the Federal Policy for the Protection of Human Subjects, or the [https://www.hhs.gov/ohrp/regulations-and-policy/regulations/common-rule/index.html Common Rule] outlines the basic provisions for [[IRB Approval|Institutional Review Boards (IRBs)]], [[Informed Consent|informed consent]], and other aspects related to protecting the rights of human research subjects. If an institution seeks guidance on implementation of the Common Rule and other applicable federal regulations, the institution should contact the department/agency conducting or supporting the research involving human research subjects. | |||
== European Standards == | |||
For countries that are part of the European Union, the [https://gdpr-info.eu/art-1-gdpr/ General Data Protection Regulation (GDPR)] lays down rules relating to the protection of human research subjects in terms of [[Data Analysis|data analysis]] and free movement of [[Personally Identifiable Information (PII)|personal information]]. In doing so, the GDPR protects fundamental rights and freedoms of human subjects, especially their right to the protection of '''PII'''. | |||
== Related Pages == | |||
[[Special:WhatLinksHere/Protecting_Human_Research_Subjects| Click here for pages that link to this topic.]] | |||
== Additional Resources == | == Additional Resources == | ||
* | * Berk Özler (World Bank), [https://blogs.worldbank.org/impactevaluations/research-adolescents-issues-surrounding-consent Research with adolescents: Issues surrounding consent] | ||
* | * Berk Özler (World Bank), [http://blogs.worldbank.org/impactevaluations/taking-ethics-seriously-response-1 Taking Ethics Seriously: Response #1] | ||
* Committee on the Use of Humans as Experimental Subjects (MIT), [http://couhes.mit.edu/forms-templates/ Forms and templates for IRB applications, informed consent, and authorization forms] | |||
* DIME Analytics (World Bank), [https://osf.io/5p68f/ Research Ethics & Data Security] | |||
* Gareth Knight (LSHTM), [https://blogs.lshtm.ac.uk/library/2018/01/15/gdpr-for-research-data/ GDPR for Research Data Management] | |||
* Martin Ravallion (World Bank), [https://blogs.worldbank.org/impactevaluations/taking-ethical-validity-seriously Taking Ethical Validity Seriously] | |||
* US Department of Health and Human Services (HHS), [https://www.hhs.gov/ohrp/regulations-and-policy/regulations/common-rule/index.html The 'Common Rule' for Protection of Human Subjects] | |||
[[Category: Research Ethics]] | [[Category: Research Ethics]] | ||
Latest revision as of 17:51, 14 August 2023
Research involving human subjects can pose complex ethical issues that require careful thought and consideration on the part of both researchers and participants. Research teams must seek ethics certifications for human subjects approval to apply for and obtain IRB approval and to protect the rights and welfare of study participants in a research project. This page will discuss the when, how, and who of ethics certifications for human research subjects.
Read First
- The DIME Research Ethics Standards discuss the provisions for protecting human subjects in development research.
- To protect the rights and welfare of study participants, IRBs require ethics certifications; depending on IRB requirements, these may be obtained via NIH, CITI, or elsewhere.
- Besides protecting human research subjects, the research team must also keep in mind best practices for IRB approval, informed consent, de-identification, and encryption.
Overview
As a prerequisite for IRB approval, all members of the research team who manage personally identifiable information (PII) must obtain ethics certifications to conduct research with human subjects. This may include principal investigators, research assistants, field coordinators, and/or survey firm staff. Two commonly accepted sources of certification are:
- The Protecting Human Research Participants Online Training
- The Collaborative Institutional Training Initiative (CITI) Training
These courses cover the historical development of human subject protections, discuss the ethical issues involved in this human subjects research, and present the principles and regulations governing it. They are divided in modules that provide reading materials and entail quizzes for which a minimum score is required to pass each module. Learners may complete the modules at their own pace.
Certificates usually have expirations and must be renewed. The CITI certificate must be renewed every 3 years, whereas the expiration of the NIH depends. Note that the IRBs can also define a date past which the certificates are considered invalid.
United States Standards
In the United States of America, the Federal Policy for the Protection of Human Subjects, or the Common Rule outlines the basic provisions for Institutional Review Boards (IRBs), informed consent, and other aspects related to protecting the rights of human research subjects. If an institution seeks guidance on implementation of the Common Rule and other applicable federal regulations, the institution should contact the department/agency conducting or supporting the research involving human research subjects.
European Standards
For countries that are part of the European Union, the General Data Protection Regulation (GDPR) lays down rules relating to the protection of human research subjects in terms of data analysis and free movement of personal information. In doing so, the GDPR protects fundamental rights and freedoms of human subjects, especially their right to the protection of PII.
Related Pages
Click here for pages that link to this topic.
Additional Resources
- Berk Özler (World Bank), Research with adolescents: Issues surrounding consent
- Berk Özler (World Bank), Taking Ethics Seriously: Response #1
- Committee on the Use of Humans as Experimental Subjects (MIT), Forms and templates for IRB applications, informed consent, and authorization forms
- DIME Analytics (World Bank), Research Ethics & Data Security
- Gareth Knight (LSHTM), GDPR for Research Data Management
- Martin Ravallion (World Bank), Taking Ethical Validity Seriously
- US Department of Health and Human Services (HHS), The 'Common Rule' for Protection of Human Subjects