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Rather than deliberately infecting subjects with the disease, the subjects could simply be observed and regularly tested to see if they have developed the illness going about their usual business.  If the control and intervention groups are large enough and the observation occurs over a long enough period, there should still be enough outcomes to be useful.  It will be important to ensure that any participants who become ill (either through contracting the illness or from side effects, etc) should be provided with treatment.  Steps should also be taken to educate both groups about prevention.  It is essential that all participants are fully informed of the risks of being in either group (control or intervention) and they should clearly understand the supports that will be available to them.

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Explain clearly on some risks involved when conducting research. A clear understanding and respect on their cultural and religious backgrounds. Explain to people who are interested in research the commitment is involved and understand the research and why we are investigating prior to signing documentation.

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participants in the study need to be able to prove they understand the risks involved. they also need to have good access to healthcare if there are any side effects. It should be made sure that there is no coercion like someone who is from a low income area wanting to make fast money. the participant needs to equally benefit from the study.

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 An ethical way to conduct research need to fulfil four basic requirements:   Researchers need to explain benefits and side effects of clinical trial to participants honestly. Clinical trial needs to have a lot of benefits to participants and community and minimal physical, emotional, psychological, financial, social, or legal harm to participants.Researchers need to get informed consent from participants.All participants of the research need to be treated fairly such as recruitment of participants, study procedures, distribute of benefits, access of benefits and end results of research to be available for all participants.

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 An ethical way to conduct research need to fulfil four basic requirements:   Researchers need to explain benefits and side effects of clinical trial to participants honestly. Clinical trial needs to have a lot of benefits to participants and community and minimal physical, emotional, psychological, financial, social, or legal harm to participants.Researchers need to get informed consent from participants.All participants of the research need to be treated fairly such as recruitment of participants, study procedures, distribute of benefits, access of benefits and end results of research to be available for all participants.

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People need to be aware of the risks vs the benefits, they need to be sure that they understand that the study may not be ethical and that it won't necessarily help existing people with diseases.

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In palliative patients does early medication intervention decrease patient suffering compared with no/late medication intervention. 

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In palliative patients does early medication intervention decrease patient suffering compared with no/late medication intervention. 

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P-Palliative patients
I-Medications
C-no/late medication intervention
O-Suffering

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To make research for vaccines and treatments ethical, there needs to be clear reasons why the research is needed, certainty that there is minimal or no risk to volunteers, and that each volunteer understands the risks via informed consent approved by HRECs

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making people aware of the vaccine, what it is used for to prevent which illness or disease and aware of risks and side effects 

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making people aware of the vaccine, what it is used for to prevent which illness or disease and aware of risks and side effects 

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Participants and their families need detailed information highlighting both benefits and risks involved. This should also include the cost of participating in the study in terms of time investment. Additionally, the financial gain should be eliminated as it presents a loop hole for abuse and a lack of proper cost/benefit analysis by participants especially from poor backgrounds.

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All health related experimental research must be met with the highest of ethical and moral standards to protect all of the parties involved. There must be processes, procedures and policies in place that cover all aspects of risk, harm, benefit and documentation must comply with all legal and ethical quality and safety considerations. 

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All health related experimental research must be met with the highest of ethical and moral standards to protect all of the parties involved. There must be processes, procedures and policies in place that cover all aspects of risk, harm, benefit and documentation must comply with all legal and ethical quality and safety considerations. 

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research and experiments related to health are generally quite polarising, with the main common answer being at the core of the study, will this research benefit the greater good?
however, risk and harm can occur therefore in order to ensure an ethical study occurs participants must obtain informed consent, be aware of all the risks and benefits of the study, anonmity just to name a few.
i agree with another student on this post that it is unethical to use money as a way to encourage people to participate, and this targets lower SES groups.

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to conduct a research to test vaccines and treatments in an ethical way the participant must be made aware of risks, benefits. they must not be forced to participate and must fully understand what is required of them

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To test vaccines on humans, we need to have (1) a compelling scientific rationale, (2) minimise risks to volunteers and (3) detailed informed consent ethical guidelines.
Volunteers should also have treatment for the disease at no cost.
I do not believe financial incentives are appropriate because this may unwittingly target disadvantaged or vulnerable populations