Learn to frame clinical trial question | clinical research courses

 

In clinical trials, it is mandatory for trial participants to submit the informed consent forms which consist of set of questions. Thus, the clinical research courses are perfect options for individuals to learn how to design the inclusive consent forms in order to stay away from unforeseen mishaps in future reference of trials.

·         Problem statement: If the chosen health problem is significant enough to research on.

                                      If the chosen study could have broader applications of useful research.

·         Relevance of context: If any pre-existing researches that showed the need for further analysis.

·         Validity of information: If the study is analyzed enough to draw gainful insights from the results.

·         Practicality of the study: If the study has broader application or is specific to a certain disease.

·         Emphasis on patients: If the study’s focus is aligned with the priorities of patients and not any physician or institution.

·         Cost effective: If the expenditure on the study was worthy enough or not.

                           If the study has any outliers that could lead to rejection and thus loss of money.

·         Viability: If the relevance of study is possible to be carried out in real conditions.

·         Assurance: If the integrity of the study would be verified and would be free of biases.

 

The clinical research is further categorized into two main types — clinical trials (interventional studies) and observational studies. Both types of studies are discussed in detail in the clinical research courses to help individuals learn more in-field concepts.

 

Clinical trials

During clinical trials, a different therapy is planned as researcher’s protocol and given to the participants. They are prescribed certain medications, surgeries along with dietary changes as a part of treatment. Clinical research courses help individuals learn about the concepts that are applicable in drug development phases of the process. Such as designing active placebo in clinical trials as medical strategy by comparing it with already available medicine/drug. Participants could also be told to have no medical or surgical intervention if needed. Later, the given treatments of specific patients are evaluated and analyzed understand their effectiveness and safety.

Observational study

In an observational study, a set of protocols or strategy is decided for evaluating the patient groups’ health status. Participants are given interventions as a part of their usual medical care either in the form of drugs, equipment or surgery. But, the investigator does not randomly assign individuals to particular interventions (unlike clinical trial). For instance, researchers may try to find out more about lifestyle changes that affect cardiac heath by monitoring a group of senior citizens.  In observational studies researchers observe patients on their current treatment plan and track their changes in health, these can be learned in the clinical research courses.

In a nutshell, clinical research courses allow individuals to learn concepts which are applied on wide range of areas such as observational studies, clinical trials, investigational studies and others. Also, clinical research courses elaborate upon cues to look out for while implementing the technical concepts into real trial scenarios.

With the clinical research courses there is also another courses which observe and detects the side effects and adverse effects of the drugs on the patients that is pharmacovigilance courses.

Recommendation:  TechnoBridge assures guaranteed placement in their Clinical research courses.