Which is an example of a carefully researched set of therapeutic procedures?
D : Validation therapy offers a good example of a carefully researched set of therapeutic procedures. Which of the following statements is not true? B : Emotionally-focused couple therapy is based on considerable research.
What is a clinical research study?
The idea for a clinical research study-also known as a clinical trial-often starts in the laboratory. After researchers test new therapies or procedures in the laboratory and in animal studies, the most promising experimental treatments are moved into clinical trials, which are conducted in phases.
What happens during a clinical trial?
After researchers test new therapies or procedures in the laboratory and in animal studies, the most promising experimental treatments are moved into clinical trials, which are conducted in phases. During a trial, more information is gained about an experimental treatment, its risks, and its effectiveness.
What does the FDA do in clinical trials?
Rather, we oversee the people who do. FDA staff meet with researchers and perform inspections of clinical trial study sites to protect the rights of patients and to verify the quality and integrity of the data. Learn more about the Drug Development Process.
What is the cell cycle?
The cell cycle represents the coordinated sequence of events in the life of a cell from its formation to its division into two daughter cells. Most of the key events of the cell cycle are restricted to a specific time within the cycle. In this exercise, you will identify when various events occur during the cell cycle.
How is cytokinesis accomplished in animal cells?
Cytokinesis in animal cells is accomplished by constriction of the cell along the plane of cell division (formation of a cleavage furrow). In plant cells, which have cell walls, a completely different mechanism of cytokinesis has evolved.
What is clinical research?
Clinical research is much different from the medical treatment you receive in a Healthcare Provider's office. Answers specific questions through research involving numerous research volunteers. Address the needs of individual patients.
Where does a clinical research study start?
The idea for a clinical research study—also known as a clinical trial—often starts in the laboratory. After researchers test new therapies or procedures in the laboratory and in animal studies, the most promising experimental treatments are moved into clinical trials, which are conducted in phases. During a trial, more information is gained about ...
How does the FDA work?
FDA works to protect participants in clinical trials and to ensure that people have reliable information before deciding whether to join a clinical trial. The Federal government has regulations and guidelines for clinical research to protect participants from unreasonable risks.
What to do before joining a clinical trial?
Before joining a clinical trial, it is important to learn as much as possible. Discuss your questions and concerns with members of the health care team conducting the trial. Also, discuss the trial with your health care provider to determine whether or not the trial is a good option based on your current treatment.
What does the FDA do?
FDA seeks to ensure that people of different ages, races, ethnic groups, and genders are included in clinical trials. Learn more about FDA’s efforts to increase diversity in clinical trials.
Why is confidentiality important in clinical research?
Confidentiality is an important part of clinical research and ensures that personal information is seen only by those authorized to have access. It also means that the personal identity and all medical information of clinical trial participants is known only to the individual patient and researchers.
What are the criteria for clinical trials?
All clinical trials have guidelines, called eligibility criteria, about who can participate. The criteria are based on such factors as age, sex, type and stage of disease, previous treatment history, and other medical conditions.