I am a volunteer

Guide for participants

On our platform, we bring together those who wish to help in scientific research with studies that test new treatments and therapies. Volunteers have the opportunity to benefit individually and be part of medical advancement.

Sections

Are you aware of the goal of your study?

Phases of a clinical trial

  • Pre-clinical phase

    (In vitro / animals)

    Studies the efficacy and safety of a component or technique.

  • Phase I

    The main objective is to evaluate safety in humans and guide the most appropriate dosage and administration regimen.

  • Phase II

    Measures efficacy and establishes the optimal dose to achieve the desired response.

  • Phase III

    Evaluates effectiveness and side effects compared to a control group.

  • Phase IV

    Evaluates unassessed aspects such as rare side effects or interactions in post-marketing.

Study characteristics

Design

  • Open trial

    Both the participant and the research team know the treatment being administered to the participant.

  • Single-blind trial

    The participant does not know the treatment group they belong to. However, the research team knows the treatments for each participant.

  • Double-blind trial

    Neither the participants nor the research team know the treatment group assignments.

Stages of a study

  • 1

    Participant selection

    Searching for individuals who meet the study’s inclusion criteria (and do not meet any of the exclusion criteria).

  • 2

    Clinical follow-up of participants

    Conducting visits, study procedures, and data collection according to the parameters defined in the protocol.

  • 3

    Study completion

    Conducting the last study visit for the last participant and closing the database where all information has been collected.

  • 4

    Result analysis

    Data export for analysis and interpretation to address the study’s hypotheses and objectives. Findings are published in scientific journals and presented at specialized conferences to contribute to the scientific community’s knowledge.

  • Stages of a study

  • 1

    Participant selection

    Searching for individuals who meet the study’s inclusion criteria (and do not meet any of the exclusion criteria).

  • 2

    Clinical follow-up of participants

    Conducting visits, study procedures, and data collection according to the parameters defined in the protocol.

  • 3

    Study completion

    Conducting the last study visit for the last participant and closing the database where all information has been collected.

  • 4

    Result analysis

    Data export for analysis and interpretation to address the study’s hypotheses and objectives. Findings are published in scientific journals and presented at specialized conferences to contribute to the scientific community’s knowledge.

The decision to participate in a clinical study is personal and should be made voluntarily, without external pressure. Whether individuals are in good health or have a medical diagnosis, they should only get involved in clinical research if they feel well-informed and comfortable with the entire process.

The decision to participate in a clinical study is personal and should be made voluntarily, without external pressure. Whether individuals are in good health or have a medical diagnosis, they should only get involved in clinical research if they feel well-informed and comfortable with the entire process.

  • Participant rights

    • Right to informed consent
    • Right to data confidentiality
    • Right to informed consent and to withdraw from the study
    • Right to receive appropriate and specialized medical care
    • Right to know the risks and benefits
    • Right to be informed about the study's progress
    • Right to study review by an ethics committee

  • Participant responsibilities

    • Responsibility to comply with the study protocols
    • Responsibility to communicate with the research team
    • Responsibility to attend scheduled visits
    • Responsibility to report side effects or problems
    • Responsibility to follow data management instructions
    • Responsibility to a continuous commitment
    • Responsibility to provide a complete medical history

  • Informed consent

    It is a key element in all clinical research as it ensures that individuals are fully informed about a research study they wish to participate in before agreeing to take part. Research team members explain the study details to each potential participant. They discuss the questions the study seeks to answer, the possible risks and benefits of participation, and the intervention being tested. They also explain what is expected of participants as part of the study. Only after individuals indicate that they fully understand these details can they freely decide to accept (or decline) participation. Participation in clinical research is always voluntary, and participants have the freedom to leave the study at any time.

Useful information

What to know before starting as a volunteer in a study?

We understand that deciding to participate in a study is a significant step. Below, you will find some essential questions that will help you make an informed decision:

  • What is the main objective of the study and how long will it last? What is expected of me as a participant?
  • Does the study involve an existing treatment or is something new being tested? Will my medical team know what treatment I am being given?
  • Will I have to pay anything to participate in the study? Will travel expenses be reimbursed?
  • Can I continue seeing my own doctor during the study?
  • If the treatment works, can I continue using it after the study?
  • Will I receive any care after the study ends?
  • If I decide to leave the study, how will this affect my medical care?
  • Do the researchers have any financial interest in the study? How much experience does the research team have?
  • How is safety ensured during the study? Will my data be confidential?
  • Can I travel?

Do you want to participate as a volunteer?

Learn about the available clinical studies.

Go to the clinical studies