1.
Which of these is the minimum number of members a SOCRA IRB is expected to have?
Correct Answer
D. 5
Explanation
A SOCRA IRB is expected to have a minimum of 5 members. An IRB (Institutional Review Board) is a committee that reviews and approves research involving human subjects to ensure ethical standards are met. SOCRA (Society of Clinical Research Associates) is an organization that promotes ethical clinical research practices. Having a minimum of 5 members ensures that the IRB has enough diversity and expertise to effectively review research protocols.
2.
Which of these guidelines is not used in clinical research?
Correct Answer
B. Criminal Record
Explanation
Clinical research focuses on studying the effectiveness and safety of medical interventions in human subjects. It primarily involves assessing medical records, age-related factors, and exposure history to determine the outcomes of the research. Criminal records, on the other hand, are not typically used as a guideline in clinical research as they are not directly relevant to the medical aspects being studied. Therefore, the correct answer is "Criminal Record."
3.
Which of these is a risk usually associated with a clinical research study?
Correct Answer
D. Linkages
Explanation
A risk usually associated with a clinical research study is the presence of linkages. Linkages refer to the connections or associations between different variables or factors in the study. These linkages can introduce bias or confounding factors that may affect the validity and reliability of the study results. It is important to identify and account for these linkages to ensure accurate and unbiased findings in clinical research studies.
4.
What is the process of learning key facts before a clinical research called?
Correct Answer
A. Informed Consent
Explanation
Informed Consent refers to the process of learning key facts before a clinical research. It involves providing all necessary information about the study, including its purpose, procedures, potential risks and benefits, and any alternatives, to the participant. The participant is then given the opportunity to ask questions and make an informed decision about whether or not to participate in the research. This process ensures that participants have a clear understanding of the study and can provide their consent voluntarily.
5.
Which board approves all clinical studies in the U.S?
Correct Answer
A. IRB
Explanation
The Institutional Review Board (IRB) is the board that approves all clinical studies in the U.S. They ensure that the studies are conducted ethically and in compliance with regulations to protect the rights and welfare of human subjects involved in the research. The IRB reviews study protocols, informed consent forms, and any potential risks or benefits associated with the study before granting approval. This board plays a crucial role in safeguarding the well-being of participants and maintaining the integrity of clinical research.
6.
What type of disease does the NIEHS study?
Correct Answer
B. Environmental
Explanation
The NIEHS study focuses on environmental diseases. This means that they research and study diseases that are caused by or related to environmental factors such as pollution, toxins, and other external influences. By studying these diseases, the NIEHS aims to understand their causes, effects, and develop strategies for prevention and treatment.
7.
What type of disease does the NIEHS classify cancer as?
Correct Answer
B. Environmental
Explanation
The NIEHS classifies cancer as an environmental disease because it is caused by various external factors in the environment such as exposure to chemicals, radiation, and pollutants. These environmental factors can increase the risk of developing cancer by damaging DNA and disrupting normal cell functioning. While genetics and individual lifestyle choices also play a role in cancer development, the NIEHS recognizes the significant impact of environmental factors in the onset and progression of the disease.
8.
Which of these is an asthma classified under?
Correct Answer
D. Environmental
Explanation
Asthma is classified under "Environmental" because it is a respiratory condition that is triggered by various environmental factors such as allergens (e.g. dust mites, pollen), air pollution, tobacco smoke, and certain chemicals. These environmental triggers can cause inflammation and constriction of the airways, leading to symptoms like wheezing, coughing, and difficulty breathing. Therefore, asthma is not classified under "Chemical," "Nuclear," or "Biological," as these categories do not specifically relate to the environmental factors that contribute to the development and exacerbation of asthma.
9.
What risk is usually associated with taking medications?
Correct Answer
C. Side effects
Explanation
Taking medications is usually associated with the risk of experiencing side effects. Side effects are unwanted or unintended effects that can occur when taking medication. These can range from mild symptoms such as drowsiness or nausea, to more serious reactions like allergic reactions or organ damage. It is important for individuals to be aware of the potential side effects of any medication they are taking and to consult with their healthcare provider if they have any concerns.
10.
Why does a statistician need to take a CCRP exam?
Correct Answer
A. Research purposes
Explanation
A statistician needs to take a CCRP exam for research purposes. This exam is likely to cover topics related to research methodology, data analysis, and statistical techniques. By passing the exam, the statistician demonstrates their knowledge and proficiency in these areas, which is crucial for conducting high-quality research. The exam may also be a requirement for certain positions or certifications in the field of statistics.