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Aryabhatta Knowledge University
Aryabhatta Centre of Nanoscience &
Nanotechnology
Manu Shreshtha
19601601008
MTech Nanoscience & Nanotechnology (2019-21)
Aryabhatta Center For Nanoscience & Nanotechnology
Aryabhatta Knowledge University, Patna
Presentation
on
Ethics With Respect To Science & Research
Guided by:
Dr Rakesh Kumar Singh
ETHICS WITH RESPECT
TO SCIENCE AND
RESEARCH
By: Manu Shreshtha
Content
1. Definition
2. Whatethicsisandwhatisitnot?
3. Ethical Theories
4. Historical Events & Development of Code of Ethics
i. Nazi Medical Experiments (1933-1945)
ii. Nuremberg Code-1949
iii. Declaration of Helsinki (1964)
iv. Tuskegee Syphilis Study 1932
v. Willowbrook Study (1950-1970)
vi. Jewish Chronic Disease Hospital Study 1960
Content
6. Importance of Ethics in Research
7. The Principle of Respect For Human Dignity
8. Informed Consent
9. Vulnerable Subject
10. Ethical Concerns in Qualitative Research
11. Ethical Concerns in Quantitative Research
12. Conclusion
13. Reference
◦ ETHICS-Greek word: ethos=custom or convention, or the spirit of community
◦ Moral principles that govern a person’s behaviour or the conducting of an activity: Oxford
dictionary (2014)
◦ The branch of philosophy that deals with morality. Ethics is concerned with distinguishing
between good and evil in the world, between right and wrong human actions, and between
virtuous and non virtuous characteristics of people- The American Dictionary of Cultural
Literacy (2005)
Definition
What ethics is and what is it not?
What is Ethics?
◦ About commitment to positive values
◦ A communal activity, applying rational principles
and universal standards to social life
◦ About real power relations and responsible power
sharing
◦ About active participation in a moral community
◦ Problem solving activity
◦ Educational process
What is not Ethics?
◦ About negative code of conduct, moral
prohibitions, disciplinary rules
◦ A private matter, nor about subjective feelings,
personal attitudes and choices
◦ Introspective self examination, or judging one’s
or other’s moral state
◦ Personal reliance on experts, lawyers,
philosophers or religious authorities
◦ Interminable disputes, or insoluble dilemma
◦ Occult process
Ethical Theories
◦ Deontology- duty is the basis of all action
◦ Teleology- actions can only judged on the basis of consequences they produce
◦ Utilitarianism-central concern is ‘the general welfare rather than individual’s interest’
Historical Events & Development of Code of
Ethics
◦ Nazi Medical Experiments (1933-1945)
◦ Nuremberg Code-1949
◦ Declaration of Helsinki (1964)
◦ Tuskegee Syphilis Study 1932
◦ Willowbrook Study (1950-1970)
◦ Jewish Chronic Disease Hospital Study 1960
Nazi Medical Experiments (1933-1945)
◦ Atrocious, unethical activities implemented in Third Reich in Europe from 1933-1945
◦ Programs included sterilisation, euthanasia, and numerous medical experiments in Nazi
concentration camps
◦ Sterilised Jews whom Nazis considered as racial enemies
◦ Medical experiments involved exposing to high altitudes, freezing temperature, malaria, poisons,
typhus fever, untested drugs and surgery without anaesthesia
◦ Selection of subjects was racially based
◦ Subjects had no opportunity to refuse the participation
Nuremberg Code-1949
◦ Mistreatment of human subjects in Nazi experiments led to the development of Nuremberg
Code (1949)
◦ Nuremberg Code contains guidelines for
o Voluntary consent
o Withdrawal of subjects from study
o Protection of subjects from physical and mental suffering, injury, disability, and death
o The balance of benefits and risks in the study
Declaration of Helsinki (1964)
◦ Greater care can be exercised to protect subjects from harm
◦ Strong, independent justification for exposing a healthy volunteer to substantial risk of
harm
◦ Investigators must protect life and health of research subjects
Tuskegee Syphilis Study 1932
◦ U S Public Health Service initiated the study in town of Tuskegee,Alabama
◦ Research subjects were divided into two groups
◦ One group of 400 men who had untreated syphilis
◦ Control group of 200 men without syphilis
Willowbrook Study (1950-1970)
◦ Research on hepatitis by Dr.Krugman at Willowbrook among mentally retarded children
◦ Early subjects were fed extracts of stool from infected individuals
◦ Later subjects received injections of purified virus
◦ Parents were forced to give permission for the child to be a subject
Jewish Chronic Disease Hospital Study 1960
◦ Study conducted to determine patients’ rejection responses to live cancer cells
◦ Twenty two patients were injected with a suspension containing live cancer cells
◦ Physician from Sloan-Kettering Institute for cancer research directed the study
◦ Study conducted without the informed consent
Importance of Ethics in Research
◦ Protects the vulnerable group and other study participants
◦ Participants are safeguarded from exploitation
◦ Establishes risk-benefit ratio for study subjects
◦ Ensures fullest respect, dignity, privacy, disclosure and fair treatment for subject
◦ Builds capability of subjects to accept or reject participation in study
The Principle of Respect For Human Dignity
◦ The right to self determination-Humans should be treated as autonomous agents, capable of
controlling their own activities
◦ The right to full disclosure-Researcher should fully describe the nature of study, subject’s right to
refuse participation, researcher’s responsibility and risks and benefits
Informed Consent
◦ Participants have adequate knowledge regarding research, have the power of choice,
enabling to decline participation voluntarily.
◦ Informed assent-the process where by minors may agree to participate in clinical trials.
Vulnerable Subject
◦ Infants, children and young people
◦ Older adults
◦ People with mental illness and people who reside in care settings
◦ People with disabilities/ learning disabilities
Ethical Concerns in Qualitative Research
◦ Distress
◦ Misinterpretation
◦ Identification
◦ Inconvenience
Ethical Concerns in Quantitative Research
◦ Related to the stage of research
◦ Formulating the research questions
◦ Designing the study
◦ Collecting data
◦ Analysis
◦ Reporting
Conclusion
◦ If research is based on a robust design and in a safe and ethical manner, it can be of benefit to all
◦ Professional codes, laws, regulations, and ethics committees can provide guidance but ultimate
determinant rests with researcher’s value system and moral code
Reference
1. Ethics of Scientific Research, By O'Neill Professor of Philosophy and Concurrent Professor of Biological Science
Kristin Shrader-Frechette, Kristin Sharon Shrader-Frechette.
2. Stern, J. E., & Elliott, D. (1997). The ethics of scientific research : A guidebook for course development. Hanover, NH:
University Press of New England.
3. Ethics and scientific publication, Dale J. Benos, Jorge Fabres, John Farmer, Jessica P. Gutierrez, Kristin Hennessy, David
Kosek, Joo Hyoung Lee, Dragos Olteanu, Tara Russell, Faheem Shaikh, and Kai Wang.
4. The ethics of scientific research: an analysis of focus groups of scientists and institutional representatives, Wenger NS1,
Korenman SG, Berk R, Berry S.
5. Teaching scientific integrity and research ethics, GerlindeSponholz, Department of Legal Medicine, University of Ulm,
Albert-Einstein-Allee 47, 89081 Ulm, Germany
6. Ethics of Scientific Publication, Derek J. De Solla Price

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Scientific Research And Ethics by Manu Shreshtha

  • 1. Aryabhatta Knowledge University Aryabhatta Centre of Nanoscience & Nanotechnology Manu Shreshtha 19601601008 MTech Nanoscience & Nanotechnology (2019-21) Aryabhatta Center For Nanoscience & Nanotechnology Aryabhatta Knowledge University, Patna Presentation on Ethics With Respect To Science & Research Guided by: Dr Rakesh Kumar Singh
  • 2. ETHICS WITH RESPECT TO SCIENCE AND RESEARCH By: Manu Shreshtha
  • 3. Content 1. Definition 2. Whatethicsisandwhatisitnot? 3. Ethical Theories 4. Historical Events & Development of Code of Ethics i. Nazi Medical Experiments (1933-1945) ii. Nuremberg Code-1949 iii. Declaration of Helsinki (1964) iv. Tuskegee Syphilis Study 1932 v. Willowbrook Study (1950-1970) vi. Jewish Chronic Disease Hospital Study 1960
  • 4. Content 6. Importance of Ethics in Research 7. The Principle of Respect For Human Dignity 8. Informed Consent 9. Vulnerable Subject 10. Ethical Concerns in Qualitative Research 11. Ethical Concerns in Quantitative Research 12. Conclusion 13. Reference
  • 5. ◦ ETHICS-Greek word: ethos=custom or convention, or the spirit of community ◦ Moral principles that govern a person’s behaviour or the conducting of an activity: Oxford dictionary (2014) ◦ The branch of philosophy that deals with morality. Ethics is concerned with distinguishing between good and evil in the world, between right and wrong human actions, and between virtuous and non virtuous characteristics of people- The American Dictionary of Cultural Literacy (2005) Definition
  • 6. What ethics is and what is it not? What is Ethics? ◦ About commitment to positive values ◦ A communal activity, applying rational principles and universal standards to social life ◦ About real power relations and responsible power sharing ◦ About active participation in a moral community ◦ Problem solving activity ◦ Educational process What is not Ethics? ◦ About negative code of conduct, moral prohibitions, disciplinary rules ◦ A private matter, nor about subjective feelings, personal attitudes and choices ◦ Introspective self examination, or judging one’s or other’s moral state ◦ Personal reliance on experts, lawyers, philosophers or religious authorities ◦ Interminable disputes, or insoluble dilemma ◦ Occult process
  • 7. Ethical Theories ◦ Deontology- duty is the basis of all action ◦ Teleology- actions can only judged on the basis of consequences they produce ◦ Utilitarianism-central concern is ‘the general welfare rather than individual’s interest’
  • 8. Historical Events & Development of Code of Ethics ◦ Nazi Medical Experiments (1933-1945) ◦ Nuremberg Code-1949 ◦ Declaration of Helsinki (1964) ◦ Tuskegee Syphilis Study 1932 ◦ Willowbrook Study (1950-1970) ◦ Jewish Chronic Disease Hospital Study 1960
  • 9. Nazi Medical Experiments (1933-1945) ◦ Atrocious, unethical activities implemented in Third Reich in Europe from 1933-1945 ◦ Programs included sterilisation, euthanasia, and numerous medical experiments in Nazi concentration camps ◦ Sterilised Jews whom Nazis considered as racial enemies ◦ Medical experiments involved exposing to high altitudes, freezing temperature, malaria, poisons, typhus fever, untested drugs and surgery without anaesthesia ◦ Selection of subjects was racially based ◦ Subjects had no opportunity to refuse the participation
  • 10. Nuremberg Code-1949 ◦ Mistreatment of human subjects in Nazi experiments led to the development of Nuremberg Code (1949) ◦ Nuremberg Code contains guidelines for o Voluntary consent o Withdrawal of subjects from study o Protection of subjects from physical and mental suffering, injury, disability, and death o The balance of benefits and risks in the study
  • 11. Declaration of Helsinki (1964) ◦ Greater care can be exercised to protect subjects from harm ◦ Strong, independent justification for exposing a healthy volunteer to substantial risk of harm ◦ Investigators must protect life and health of research subjects
  • 12. Tuskegee Syphilis Study 1932 ◦ U S Public Health Service initiated the study in town of Tuskegee,Alabama ◦ Research subjects were divided into two groups ◦ One group of 400 men who had untreated syphilis ◦ Control group of 200 men without syphilis
  • 13. Willowbrook Study (1950-1970) ◦ Research on hepatitis by Dr.Krugman at Willowbrook among mentally retarded children ◦ Early subjects were fed extracts of stool from infected individuals ◦ Later subjects received injections of purified virus ◦ Parents were forced to give permission for the child to be a subject
  • 14. Jewish Chronic Disease Hospital Study 1960 ◦ Study conducted to determine patients’ rejection responses to live cancer cells ◦ Twenty two patients were injected with a suspension containing live cancer cells ◦ Physician from Sloan-Kettering Institute for cancer research directed the study ◦ Study conducted without the informed consent
  • 15. Importance of Ethics in Research ◦ Protects the vulnerable group and other study participants ◦ Participants are safeguarded from exploitation ◦ Establishes risk-benefit ratio for study subjects ◦ Ensures fullest respect, dignity, privacy, disclosure and fair treatment for subject ◦ Builds capability of subjects to accept or reject participation in study
  • 16. The Principle of Respect For Human Dignity ◦ The right to self determination-Humans should be treated as autonomous agents, capable of controlling their own activities ◦ The right to full disclosure-Researcher should fully describe the nature of study, subject’s right to refuse participation, researcher’s responsibility and risks and benefits
  • 17. Informed Consent ◦ Participants have adequate knowledge regarding research, have the power of choice, enabling to decline participation voluntarily. ◦ Informed assent-the process where by minors may agree to participate in clinical trials.
  • 18. Vulnerable Subject ◦ Infants, children and young people ◦ Older adults ◦ People with mental illness and people who reside in care settings ◦ People with disabilities/ learning disabilities
  • 19. Ethical Concerns in Qualitative Research ◦ Distress ◦ Misinterpretation ◦ Identification ◦ Inconvenience
  • 20. Ethical Concerns in Quantitative Research ◦ Related to the stage of research ◦ Formulating the research questions ◦ Designing the study ◦ Collecting data ◦ Analysis ◦ Reporting
  • 21. Conclusion ◦ If research is based on a robust design and in a safe and ethical manner, it can be of benefit to all ◦ Professional codes, laws, regulations, and ethics committees can provide guidance but ultimate determinant rests with researcher’s value system and moral code
  • 22. Reference 1. Ethics of Scientific Research, By O'Neill Professor of Philosophy and Concurrent Professor of Biological Science Kristin Shrader-Frechette, Kristin Sharon Shrader-Frechette. 2. Stern, J. E., & Elliott, D. (1997). The ethics of scientific research : A guidebook for course development. Hanover, NH: University Press of New England. 3. Ethics and scientific publication, Dale J. Benos, Jorge Fabres, John Farmer, Jessica P. Gutierrez, Kristin Hennessy, David Kosek, Joo Hyoung Lee, Dragos Olteanu, Tara Russell, Faheem Shaikh, and Kai Wang. 4. The ethics of scientific research: an analysis of focus groups of scientists and institutional representatives, Wenger NS1, Korenman SG, Berk R, Berry S. 5. Teaching scientific integrity and research ethics, GerlindeSponholz, Department of Legal Medicine, University of Ulm, Albert-Einstein-Allee 47, 89081 Ulm, Germany 6. Ethics of Scientific Publication, Derek J. De Solla Price