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Elisavet M

"Virtual Reality tackles tough questions" - 1 views

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    Scientists in Barcelona have constructed a technological device, enabling users to engage and "live" within a virtual reality; this digital world however, is bound by the oppressive and devastating human conditions experienced by the victimized individuals of physical and verbal maltreatment. The device, although it may conjure ethical realizations within the user's mind, also poses as an ethical dilemma for it brings the cruel severity of the downtrodden and exploited people into visual and mental display terrorizing the emotional stability of the participants.
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    Technological breakthroughs in decoding the human mind have blossomed ever since the invention of a device through which users are immersed within a virtual reality, to live and experience the trauma and distressing scenarios of people victimized by physical as well as emotional abuse. Developed by a team of Spanish scientists, this device is breaking down the mind's irrational judgement in relation to discriminatory or wrongful perceptions against others. The user of the device, once transported into the anguished lives of the virtual characters, comes face to face with the agony of living through abusive violence, and begins to form a clearer impression about the effects of such experiences upon the lifestyle, behavior and well being of any victim. In doing so, the participant ultimately widens the boundaries of his mental state of thought, and begins to appreciate and acknowledge the peace given by a happy life rid of gnawing internal complications. However, in engaging with such a virtual reality the user becomes an unshielded target of bitter misery, felt and illustrated by the depictions seen through the device. The software that is included in this article is the technological device that offers an entrance into the virtual world for the user. The stakeholders within this article are the users of the device, whose mental and emotional stability is controlled by the virtual reality developed by the scientists. The scientists hold the success of the entire experiment in the palm of their hands, and really are the source of the effect upon human behavior. One has to take into consideration the physical and psychological considerations (in "Health" scenario) of technology on the user of this particular device; although this device does help others modify their morality as they expand their considerations for the factors that have made people what they are today. The device however, does inflict the same trauma and terror depicted by the gestures and movements
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    I agree with the ethical and social concerns involved within your article. Although there are some benefits of recognizing the pain and violence inflicted on others, it can cause emotional stigma and trauma upon the person who is using this technological device. Technology controls our ethical morality, in developing software that explores the way the human brain works we destroy this boundary of what is right and wrong because we begin to focus on research and forget the effects involved. In this case, those involved in the experiment are unaware of the effects that this virtual reality exposed to the user will eventually have on them mentally and emotionally.
Madeline Brownstone

Your Brain on Google Study Tells Us Nothing New | World of Psychology - 0 views

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    "To study what brains look like when people are searching the Internet"
Madeline Brownstone

NOVA Online | Cracking the Code of Life | Watch the Program - 7 views

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    Please use this bookmark to post your reflections. Using a Paper 2 style approach, CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. CRITERION D) Evaluate the efficacy of a solution to the problem.
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    Criterion A- The IT system (research DNA database) that allows medical researchers to record and track medical histories throughout generations, arise a variety of issues. One of these issues is privacy, where the database holds genetic information that many ethical doctors call a "future diary". These medical databases can be analyzed by a variety of people and those who have access to this information are handling private information. The major stakeholders were those patients who gave up their DNA because their genetic information put into the hands of these medical doctors creates the privacy issue. This information needed to be well stored and doctors take implications such as encoding social security numbers and no names are used. Criterion B- These research DNA databases begin with the obtainment of genetic information. In a relational database, there are several tables containing various information. Each table contains data that all have attributes related to the subject of the table. All of the tables might be interconnected, as well. For example, a retail business using a relational database would likely have one table containing data regarding employees, another with data regarding customers, another table listing inventory and so on. A database user could run a report to find connections between data in different tables, such as the customer table and the inventory table. Criterion C- From the point of view of the major stake holders (patients who given up their genetic information) the IT system (research DNA databases) (Not done)
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    Criterion A) The IT system is a database. This database is a link of DNA records, health records, and family trees. Major stakeholders of this issue are citizens of Iceland who agree to let their information be put on these databases and analyzed. Criterion B) The database works in parts. First, there is already a database of family trees in place. This family tree generator works by inputting an individual's social security number. After this is in place, the name of many generations of ancestors of this individual is shown in a tree. Then, the creator of the database asks for the permission, of family members, to add the DNA code and the health record of each person. This allows for a social security number and a disease to be input at the same time. With this, the scientist can see those who have it, and those who don't. Then, with the use of the DNA codes, they can "hunt down" genes that cause certain diseases. The database is related to an issue of privacy. This is because those who allow their health records and DNA code, are letting the medical team and users of the database know all things about them. With just a social security number, a user that has access to the database may learn more things about you than you may want: such as your family, what diseases you may have, and many other things. Another issue is in reliability. There is the possibility that the medical teams that try to track genetic code differences between those with a disease and those without it, may come to realize that a difference they find is only a coincidence and not helpful. (not completed)
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    The IT system being used is the DNA database that are being kept on the Icelandic people. The DNA database holds a lot of information of the people in the database and even things that they do not know such as their DNA and what it means. The major stakeholder is the people that are sending their DNA information, blood samples, medical histories and family trees. The issue of privacy is then involved because of the personal information that others can go through by accessing the database. The database is run by first getting the blood sample of the patient who willingly gives permission to give their DNA information to the company, deCODE. The information is then entered into the database which organizes the information by each person's social security number. The relational database is used to organize the information. (Cont.) The impacts of the database is both negative and positive. The database can be
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    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. * The IT system described in this video is a medical database. The major stakeholder are the doctors who manage the data of patients in the relational databases. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). * A relational database, there are several tables containing various information. Each table contains data that all have attributes related to the subject of the table. All of the tables might be interconnected, as well. For example, a retail business using a relational database would likely have one table containing data regarding employees, another with data regarding customers, another table listing inventory and so on. A database user could run a report to find connections between data in different tables, such as the customer table and the inventory table. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. * One of the positive impacts of these medical databases are that the family tree is in a database and all health records can be found for each patient and because this is a relational database, all of the patient's information is linked to their families and other people who have similar diseases. This is beneficial because experts can see trends in the people who have a certain disease and once they figure out the "spelling" of the genetic code with the disease, they can work on coming up for cures for that particular disease. A negative impact of the medical databases can be privacy. The doctors have access to every patients information and they can know everything about a certain person or family if he/she wanted to. This would then raise an issue of integrity.
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    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. The IT system is the database and the issue is who has access of the Database which has medical records of individuals. The major stakeholders are the Doctors and Patients. Doctors are trying to find information on specific DNA that create sickness and diseases. Finding the relationship between the family members and there DNA, can possibly improve medicine and also allow doctors figure out what an individual can have(sickness) in future references, making inferences of what might happen. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). A data base function is that it is a computer stored software that contains tables of various information and organizes all the data into categories. One subject/category can be related to another with little difference. This is why the database makes it easier for information to be viewed and interpreted much faster. By entering data on the tables one can interlink topics in order to find specific information needed. The person who enters the data can use software like Openoffice to create a database to view DNA and the relationship with the other individuals. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. The primary issue of the negative impact on Databases, have on the skateholders for DNA purposes is Privacy. Privacy has a big part in the stakeholders because many of the patient give away there Social Security number which is something private to them. With the Social Security Number the doctors can have access to other information not related in there investigation of finding a cure. This can cause reliability with the doctors to decrease. The database would have information of all sort on there medical records which should not be something that would be public for eve
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    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues: The IT system in these videos were medical databases containing records of many patients. Specialists use these databases to help them identify where a certain disease came from and whether or not it could be treated. they do this by viewing the patients ancestors records and seeing who had the disease in that family tree. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). Specialists (with the permission of the patient) insert a patients social security number into the medical database and let the database generate the patients entire family tree. Using this family tree, doctors were able to "hunt" down the origin of diseases, by looking at the genes of the ancestors. That way, by matching the DNA of the patient affected by a certain disease with the DNA of one of his/her ancestors DNA that suffered the same disease, and looking for similarities or patterns. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. There were several positive and negative impacts regarding this "hunting down" of diseases. By looking at family trees specialists and doctors would be able to determine what caused the disease and possibly come up with a cure or treatment for it. However, many patients are concerned with doctors going through their records and DNA due to there being a lack of privacy. If patients grant permission, specialists would be able to find out and know absolutely everything about their health history. Specialists argue that it would be of great benefit to detect diseases early so they could be treated by doing this. Chips are being created were thousands of babies genes could be looked at to look for any abnormalities. Some people argue that even if a disease were detected, there's two possibilities, one
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    Criterion A) The IT system at work here is the database run by the company deCODE. This company created a medical database in order to determine human diseases present amongst family. This leaves the stakeholders to be the Iceland citizens who use this system. The relationship between the Iceland citizens who use this system and the issue is that there is a security issue. The company, deCODE, paid a sum of one million dollars to the government for access to the medical history's and information of the Iceland citizens. This could be stolen by others or it could be hacked by an outsider. Criterion B) This system works through a series of steps to figure out what medical diseases are passed on throughout the family tree. In this case it would be a relational database. This database works by first obtaining permission from the Icelandic citizen to use their social security number and their medical history. This is put into the system and the medical records are accessed. Then the family records and past can be seen. This is multiple tables containing different pieces of information. Each table has something that is related to the previous table. Then make sure that the database is easily navigational. When the social security number is entered into the database the company must have it in the record. If the social security number is not properly encoded then the social security card could be stolen by and employee of an outside hacker. This is related to security if the hardware or software is not properly secured it can be obtained by a criminal. This can lead to identity theft and loss of financial security. Another issue would be privacy. The medical records and DNA code is allowed full use to the company. The social security number could be used in ways that the civilian did not agree to and is not known by the civilian. Criterion C) This system can cause many positive and negative impacts. One positive impact would be that this would help the patient know who e
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    Criterion A) The IT system at work here is the database run by the company deCODE. This company created a medical database in order to determine human diseases present amongst family. This leaves the stakeholders to be the Iceland citizens who use this system. The relationship between the Iceland citizens who use this system and the issue is that there is a security issue. The company, deCODE, paid a sum of one million dollars to the government for access to the medical history's and information of the Iceland citizens. This could be stolen by others or it could be hacked by an outsider. Criterion B) This system works through a series of steps to figure out what medical diseases are passed on throughout the family tree. In this case it would be a relational database. This database works by first obtaining permission from the Icelandic citizen to use their social security number and their medical history. This is put into the system and the medical records are accessed. Then the family records and past can be seen. This is multiple tables containing different pieces of information. Each table has something that is related to the previous table. Then make sure that the database is easily navigational. When the social security number is entered into the database the company must have it in the record. If the social security number is not properly encoded then the social security card could be stolen by and employee of an outside hacker. This is related to security if the hardware or software is not properly secured it can be obtained by a criminal. This can lead to identity theft and loss of financial security. Another issue would be privacy. The medical records and DNA code is allowed full use to the company. The social security number could be used in ways that the civilian did not agree to and is not known by the civilian. Criterion C) This system can cause many positive and negative impacts. One positive impact would be that this would help the patient know who e
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    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. The IT system involved is the DNA database system, identified as an organized collection of age old family trees, accompanied by state of the art DNA analysis and computer technology. Systematically, genetic information (DNA) is stored in related tables, distinguished by individuals' own security number codes. One centralized ethical and social consideration is privacy, mainly a major concern of the involved DNA suppliers (the public), that place their given personal information (genetic data, reference to family origins, medical history etc) in a national database system, from which the accessing of medical records and history of one's entire family can become manipulated or misused. In addition to the elevated risk of data misuse, once the involved participants (Icelandic citizens) give access to their personal information, there are no limitations placed on the utilization of the data within the national database, as it becomes accessible for the government, medical researchers and operating staff. Thus, the implications are straining to the individual donor, unable to determine when, how and to what extent the information given is shared amongst other groups. Furthermore, the privacy of the participants undesirably opens access to the medical information of related family members, as cross-referencing and data matching give the research staff operating the DNA database, access to retrieve a plethora of other members' data mainly for the purpose of effective data mining (the retrieval of hidden predictive patterns, as a diagnostic tool to decode the occurrence of genetic disorders/diseases). CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). With the possession of participant's medical data, including blood type, isolated samples of DNA, medical health records e
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    The primary IT system in use is a DNA database, which includes information about patients, illnesses, and virtually one's make up as a human. DNA databases allow researchers to find patterns in a human genome, by looking at the DNA from various family members and determining the difference or similarities between the DNA of family members. This is done through database functions such as data mining, and data matching. Locations such as Iceland, have a database that traces back all of the people within the country to their Viking ancestors. These family trees have been paired with DNA analysis in order to trace diseases back to their start. Some more tests could be conducted in order to determine which of the living relatives of one family with arthritis, for example, have the disease. Then, the DNA can be compared in order to identify the exact gene that is at fault for the disease. This process is very easy to do because the database with all of the ancestral information is accessible with the presence of one of the family member's SSN. A simple data query can then bring together all of the person's information. Moreover, DNA, health records, and the family trees of Iceland were proposed to be linked. This could be very beneficial because new drugs could be made available to suit the specific disease of a patient. It could also be a way for diagnosed patients to take early preventative measures. This could increase the probability for a cure, and in general this would increase the life expectancy of certain areas. However, some doctors in Iceland opposed to this linkage, because the information is representative of each person's medical history, and potentially their future medical history. This information, according to the plans of the linkage of medical records and the family tree, would be available on a central database that would bring together private information about a person and connect it to all of their family members, past, present, and future. T
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    There is another issue along with this involving the ability of researchers to have full access to the information about anyone. Many people want to maintain their right to privacy, but others argue that this could lead to new knowledge about diseases, and the development of new medicines. For those who are afraid of risking their privacy, there are standards developed in order to protect them. Their information, such as SSNs are encoded for security reasons and the DNA part of the project is voluntary, and not imposed. However, ethicists are still afraid of this database. They claim that the future of DNA is a valuable thing because it can predict the probability of diseases, life expectancies, etc. But all copies can be made available to the FBI, schools, etc. at the time of birth. For the Biotech Industry, this is seen as a huge advantage because people an be tested for hundreds of diseases. The awareness of the disease is a great thing, because it could lead to early prevention. However, the system is faulty because it sometimes doesn't provide certainty of a disease and it limits a person's privacy. Other times, there is no cure for the disease, so the patient cannot do anything even if they know. In relation to this, there also will arise severe psychological impacts of a person knowing that they have the possibility for getting a life threatening disease. If this is a disease that will affect them later on in life, it would be detrimental for a person to live their life without the hope of a prosperous future. A solution to this problem could be giving patients the choice of knowing or not.
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    Criterion A - The IT system is the DNA database containing information about the genetic past, present, and future of the patients. The primary issues associated with this database are of privacy and anonymity. These issues arise when patients, who are one of the major stakeholders, feel that that the information in these databases shouldn't be accessible to others, or anyone for that matter. While some believe this is private information, others believe that the information should not be known by anyone because of the ethical issues associated with knowing what will come in the future. Criterion B - The medical database is a relational database meaning that it establishes relationships between different tables in the database. The smallest building blocks of a relational database are items. Items are individual pieces of information in tables. These items are organized into fields and records. Fields are columns in a table that that represent different categories of information. Records are rows that represent all the information for a specific patient. At the cross-section of a particular record and field lies the item associated with a specific piece of information related to the specified patient. These tables are related to each other through links which are established by unique primary keys assigned to each patient. This system is related to the issue of privacy because the information contained within it is considered by many to be privileged and access to it should be very limited or altogether eliminated. Criterion C - The impacts of such a database on society are varied. Some people are very against the entire idea of a genetic database because of its ethical concerns. When people have their blood analyzed for DNA, they are giving up their genetic make-up. The information that can be obtained from such tests is considered by many to be privileged, and by others to be completely unethical in every way. Often people are against very private medical
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