Chapter One
 Chapter Two
 Chapter Three
 Chapter Four
 Chapter Five

   

Chapter Two - Additional Resources

ETHICAL PRINCIPLES FOR SOCIAL RESEARCH 

(TO BE AGREED BEFORE THE RESEARCH COMMENCES)

  • Responsibility to Research
  • The researcher should be competent and aware of what is involved in conducting research
  • The research must be conducted rigorously and with the correct procedures – avoid misuse of procedures at all stages
  • Report procedures accurately and publicly (rigour)
  • Don’t jeopardize future research(ers)
  • Report clearly and make data available for checking
  • Tell the truth (do not tell lies or falsify data, avoid being unfairly selective, e.g. to support a case, do not misrepresent data)
  • Maintain the integrity and autonomy of the research, e.g. avoid censorship of or interference with the research by sponsors/those who give permission for the research to be undertaken
  • Responsibility to Participants and Audience(s)
  • Gain fully informed consent (usually in writing), in order to respect self-determination and autonomy; provide information on all aspects of the research and its possible consequences
  • Decide whether overt or covert research is required/justified
  • Ensure non-maleficence (no harm, hurt or suffering to be caused to participants and those who might be affected by the research); be humane
  • Ensure beneficence (the research will bring benefit to the participants or will contribute to the welfare of participants)
  • Respect people’s rights and dignity and interests, and be respectful – research participants are subjects, not objects to be exploited. Treat people as subjects, not objects
  • Agree individual’s rights to privacy,
  • Ensure participants have the right to withdraw at any time
  • Inform participants who will have access to the data/report, i.e. the audiences of the research, how public it will be, when it will become public, and how it will be disseminated; negotiate levels of release (i.e. who see which parts of the research)
  • Ensure anonymity/confidentiality/non-traceability; if these are not possible then tell participants in advance
  • Indicate how anonymity will be addressed (e.g. by confidentiality, aggregation of data)
  • Inform participants how data will be collected and how files/questionnaires/audio-cassettes / video-cassettes will be stored during the research and destroyed after use)
  • Ensure sensitivity to people (e.g. age, ethnicity, gender, culture, religion, language, socio-economic status etc.)
  • Ensure honesty with people
  • Gain permission from all relevant parties (e.g. parents/guardians, principals etc.) for access
  • Respect vulnerability (e.g. in interviewing children/ those without power)
  • Agree respondent validation
  • Agree ownership of the data (and when ownership passes from participants to researcher)
  • Allow time for review
  • Avoid causing unnecessary offence
  • Ensure that participants and sponsors have the right to dissent/distance themselves from the research
  • Demonstrate social responsibility and obligations
  • Consider indemnification
  • Don’t abuse your position/power as a researcher
  • Don’t use dangerous methods


 
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