After finding a research study, what do volunteers do?

Taking part in a research project is an exciting opportunity that has many benefits. There are different types of clinical trials, each with its own goals and timelines. However, volunteers who take part in a trial will generally follow the same path. Continue reading to learn more.

What happens if I join a clinical study?

The first step after finding a research study that seems like a good match is to call and check eligibility. Typically, questions over the phone include topics like medication history, diagnosis, and any other information relevant to the inclusion criteria and exclusion criteria for the trial.

If your answers match what the study wants, you will be asked to do additional screenings and tests at a clinic. In-person screenings can include lab tests, measurements, and other metrics.

The process of informed consent

Informed Consent Process is one of the most crucial parts of participating in a clinical trial. Participants in research are given an informed consent form to help them understand the study’s nature, potential risks and rewards, and the expectations of their participation. The informed consent document provides all the information necessary to help participants make an informed choice about whether to take part in the research.

The study form is the ideal opportunity to ask any related questions, such as the schedule of visits, the record-keeping requirements, and other factors that may influence the decision to participate. This form will explain whether or not the study is placebo-controlled. It will also specify if the participants are allowed to continue the treatment if the results prove it is effective. Even after signing an informed consent form, participants may still choose to leave the trial for any reason and at any time.

Attending sessions and keeping records

Participants are officially enrolled in the trial once they have completed the informed consent process. They can then start attending sessions and keep records. A clinical trial appointment is very similar to a doctor’s appointment. However, volunteers will receive more specialized care from experts who are familiar with their condition. The trial may require visits to be made over several weeks, months, or years.

Many trials require that participants record their progress between sessions in addition to attending the in-person visit. Typically, volunteers will be asked to take notes on side effects, complete questionnaires to assess their quality of living or wear fitness trackers to monitor vital signs and daily activities.

The following-up process

The study team can provide more details about the trial results once the research has been completed. Each trial is unique so the information will vary. Many clinical trial results are published in peer-reviewed journals, which participants can access. However, they may also contact individual volunteers after the final results have been announced.

Many times, participants in research will be given the choice to continue the study or treatment if they find it effective. This is often done even before the product is on the market. The research team can guide you at any stage of the process.

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