- This topic has 16 replies, 14 voices, and was last updated 3 years, 9 months ago by
Phone Suu Khaing.
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2020-10-03 at 8:19 am #22966
Saranath
KeymasterPlease watch the VDO for topic discussion.
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2020-10-10 at 11:30 pm #23240
Pongsakorn Sadakorn
ParticipantIn this case, I will give the data out if: (i) the researcher’s team got the ethics approval from the global or national committee. (ii) The purpose of the research is clear and do not an infringement of the privacy rights of a person or group of persons. (iii) Permission letter from a higher level such as Public Health Minister is issued. (iv) The data tracking or data monitoring process has set to confirm that the data have been used and analyzed legitimately. (v) Finally, the timeline and the scope of the use of data are clear.
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2020-10-11 at 8:12 am #23243
Kridsada Sirichaisit
ParticipantI can’t send individual data to them. If research team want to get this data, they must write research proposal and ask for ethics committee. When they get EC, they use this EC to ask to director of organization that collect this database. If go pass to this process if the data include privacy personal information they must ask for information from individual patients by consent form.
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2020-10-11 at 4:22 pm #23255
Sila Klanklaeo
ParticipantI can not put the individual data out because the raw data may harm the patient and protect by the fundamental principle of privacy. If we have to provide information to them Should have obtained prior consent for the process.
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2020-10-12 at 1:34 am #23280
Saravalee Suphakarn
ParticipantIn my opinion, I can give the information to the research team which non violate any of general principles of informatics ethics, if the condition in consent form, that subjects have to sign the permission before give the information, is allowed to use the data in other research. To ensure about privacy and security of the information when are used in the research, I must request proposal of the research which detail about measure to protect the information and consider it base on the regulation on the protection of personal data.
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2020-10-18 at 3:39 pm #23399
Khaing Zin Zin Htwe
ParticipantYes, it is necessary to check the consent given by the subjects for any research purpose.
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2020-10-14 at 8:48 pm #23318
Rawinan Soma
ParticipantIn the real world, if other organizations request for the raw data of the system like surveillance data, research question, or survey data. They should submit the proposal that contain such as the objective of the study, what and how much the data will used, and how to protect the data. This proposal will be going to the ethical committee board for consideration to authorize the data access. In this situation, I will follow these protocols in order to ensure the data privacy and security. The data will be use in the beneficial way, to generate new knowledge, enhance the system, and lead to disease elimination in the country.
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2020-10-14 at 11:49 pm #23321
Ornpicha Thiampol
ParticipantI cannot send the data directly to them. I will check the consent form of patients first (If there is it) and check the official document to request the data from us. We can make sure that they will not use data in the wrong way and protect patient’s privacy. There is a possibility to share the data because it’s a benefit for patients. In this case, I think we don’t feel the need to ask for consent from patients if the advantages of the study are better for them.
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2020-10-18 at 8:00 pm #23409
Sittidech Surasri
ParticipantThank you for your comment. I would like to you to think about the Thailand Regulation on the protection of personal data (2019) and suggest the researchers team should submit their protocol to the Ethic Committee for review and approval.
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2020-10-19 at 11:45 pm #23427
Kaung Khant Tin
ParticipantI think a single person does not have any privileges to decide, by his or her own means, whether a study can be advantageous before the study starts. And yet, there’s always a need to take consent of the patients, as well as an approval from the respected professionals ,here in this case, ethical research committees.
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2020-10-15 at 1:42 am #23323
Wachirawit Supasa
ParticipantI would require the Internation Review Board approval prior to sending them any data because, at national level, there is a lot of sensitive information about each individual. IRB could screen, dispute, and argue if any information they require not necessary for the research purpose.
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2020-10-18 at 3:43 pm #23400
Khaing Zin Zin Htwe
ParticipantFor me to give the data to the research team, these 2 criteria must be fulfilled. First, there must be consent given for research purposes in the form signed by the subjects. Second, the research team can provide the approval from local ethical committee after their ethical considerations have all been addressed.
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2020-10-18 at 7:55 pm #23408
Sittidech Surasri
ParticipantPer this scenario, I will not give data to them (Western researcher) without approval and permission, and will follow the policy of organization and follow the the General Principles of Informatics Ethics as below lists:
– Keeping health records/data safe and secure
– Provide access to the record by authorized personnel
– Maintaining the integrity and of the health record
– Excellence in the professional performance in term of honesty and integrity.
– Avoid conflict of interest
If I have to provide the data to them, I would inform them that they should do protocol submission to the Ethic Committee for review and approval to use the data because it is a privacy of patient. -
2020-10-19 at 7:57 pm #23417
Naphat
ParticipantI’m unable to provide personal informations, because of the security of personal information including research ethics. There are also the consent of volunteers to allow them to do this research. If there need to request for information, they must to have the research team for prepare documents to apply for the new research to EC but I think there is no way to approve if personal information is requested in a research study.
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2020-10-19 at 11:40 pm #23426
Kaung Khant Tin
ParticipantFirst of all, I surely should not give the data out to the research team from a western country no matter they claim that their study will bring positive impact on the malaria sector.
They have to follow the standard procedure and steps if they claim they are a reputable research team. And I can guide them not violating the general principles of informatics ethics.
According to the principle of legitimate infringement, the right to the privacy and control over the data can be conditioned by the legitimate, appropriate and relevant data-needs, I will advise them to request the data from a legitimate process. And only from an approval of the research ethics committee of the ministry, I will give the required data. And in doing so, I will follow the principle of the least intrusive alternative to ensure the data is given in the least intrusive fashion and with a minimum of interference. -
2020-10-19 at 11:53 pm #23428
Navinee Kruahong
ParticipantIn term of ethics and data protection, I cannot share or use the personal data more than stated in the informed consent of research among local and migrant patients.
However, with a valid reason of benefit to population health, we should ask for permission from all local and migrant patients again about sharing their personal data, and do properly consent form. -
2020-10-22 at 12:03 am #23479
Phone Suu Khaing
ParticipantIn this case, principle of security must be respected. So, I cannot provide data out.
However, as mentioned in case scenario, the research study could provide benefit for disease prevention, we also have to consider for it.
We need approval from ethical review committee for this study.
If ethical review committee has approved it and informed to respective authorities, we could provide related data. Unless, we cannot provide any data.
Plus, we also has to respect principle of information privacy and disposition. So, we also must ask consent from group or individual as personal data such home address and disease status are included.
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