Participation in clinical trials for payment is an opportunity for many people to earn extra money. This issue is particularly relevant in times of crisis and rising unemployment. However, do not think of participation in clinical trials as an easy and simple part-time job. Participation in such projects has a number of features that you should be aware of before submitting your application.
Participation in clinical trials for payment is an opportunity for many people to earn extra money. This issue is particularly relevant in times of crisis and rising unemployment.
However, do not think of participation in clinical trials as an easy and simple part-time job. Participation in such projects has a number of features that you should be aware of before submitting your application.
Together with Clinical Research Specialists, OnlineCRF, we decided to highlight the important points regarding participation in clinical trials for money in this article. This will be useful to those who are finding such opportunities for the first time and will provide additional information to those who already have experience in participating in research.
What is a clinical trial?
A clinical trial involves testing new drugs with volunteers’ participation. The main purpose of the research is to check the safety and effectiveness of the drug before it enters the market. Nowadays, researchers are developing a vaccine for the COVID-19 pandemic.
The stage of clinical trials begins after the drug has successfully passed animal tests or cell test models.
In total, there are three stages in clinical trials. They differ in the number of participants and the objectives of the study.
Stage 1 of clinical research takes place with the participation of a small group of healthy volunteers. At this stage, the drug is checked for safety and the absence of adverse reactions. As a rule, we are talking about participation in the project for money – this applies to stage 1.
Stage 2 of clinical research is conducted with the participation of patients with a specific disease, which is being treated by the studied drug. In phase 2, a small group of volunteers is involved. This stage checks if the drug is safe and effective for the treatment of a particular disease.
Stage 3 of clinical trials also take place with the participation of patients with a specific disease. At this stage, the group of patients is much larger. The number of participants can reach several thousand. At this stage, the safety and effectiveness of the drug are also checked.
In this article, we will mainly talk about stage 1 of clinical research, since it is at this stage that healthy volunteers participate. They then receive material compensation.
Clinical trial participants must meet certain criteria
When deciding to participate in a clinical trial, volunteers may expect immediate acceptance. But this is not so. And you should be prepared for the fact that you may be denied participation for several reasons. Most of them concern health status.
Clinical trial participants are presented with a number of criteria questions regarding their state of health. They relate to the presence of chronic diseases, BMI, vital signs, etc. Before participating in the project, a volunteer undergoes an examination and passes a series of tests. Only if all indicators are normal and the person’s state of health meets the requirements, will he or she be able to become a participant in a clinical trial.
Each clinical trial has its own requirements for volunteers. These points need to be clarified in advance, to find out a list of contraindications, what chronic diseases can become an obstacle to participation, what kind of health requirements are made by the organizers, etc. This will help at the start to find a suitable project for participation.
It is important to read the documents carefully before participating
The mandatory stage before the start of the study is to fully inform the volunteer about the conditions of the project. The participant reads special documents – informed consent forms (ICF) in the presence of the researcher’s doctor. From it, he or she can learn about all the details of the project, the amount of compensation, and the procedure for payment, the conditions for exit from the project, and much more. It is very important to familiarize yourself with the document in detail and ask any questions before signing. This way, you can avoid misunderstandings and contentious issues during the project.
You can finish the study at any time
Very often, volunteers have the idea that after signing the documents, they are obliged to stay in the study until the very end, no matter what. But this is not at all true. After reading the ICF, you will see that, in most cases, you can voluntarily end your participation in the project at any stage. Therefore, as soon as you experience health problems or your plans have changed – you should inform your doctor about this and discuss a time to exit. But, keep in mind that in this case, you may not receive the full participation fee.
In general, participating in clinical trials for money is a good way to earn extra money. And besides this, you have a chance to help the development of medicine and important new drugs. However, before any research, it is important to study all the conditions for participation in the project, weigh the pros and cons, and carefully discuss all the details. Then the project will be simple and effective, both for you and for researchers.