Frequently Asked
Questions (FAQs)

Learn the Language of Clinical Studies

Informed Consent

Before joining a study, you’ll go through an informed consent process, where you’ll learn about the study's purpose, duration, potential risks, and benefits. This process allows you to make an informed choice about participating. Remember, consent is not a contract—you are free to withdraw at any time.

Protocol

A protocol is the detailed plan for a study. It outlines every step, including participant eligibility, treatment schedules, dosages, and duration. Designed to safeguard participants, the protocol ensures each trial meets strict safety and ethical standards. Our clinical team uses the protocol to monitor your health and address any questions you might have.

Placebo-Controlled

In some studies, a "placebo"
is used to compare the actual effects of the treatment. You might receive either the active medication or a placebo, and neither you nor the research team will know which you’ve been given. This approach helps us measure the real effectiveness of the treatment.

Why Choose Southwest Clinical Research?

Access Innovative Treatments

Clinical trials provide early access to advanced treatments and therapies that may not be available through standard healthcare.

Contribute to
Medical Progress

By participating, you help advance medical research, contributing to the development of new treatments for various conditions.

Receive
Compensation

We compensate eligible participants for their time and travel. Payment varies depending on the study.

Who Can Join a Clinical Trial?

Nearly anyone can participate, regardless of age, health, ethnicity, or background. Clinical trials are open to a wide range of participants, from healthy volunteers to individuals with specific medical conditions such as diabetes or asthma. Participating offers access to new treatments before they’re widely available.

Frequently Asked Questions

Can I get compensated for study participation?

Yes, eligible participants receive compensation for their time and travel expenses. The amount varies depending on the study.

What are the potential risks or benefits?

Clinical trials carry potential benefits like access to new treatments, but they may also have risks. Our team will discuss these with you during the informed consent process.

What does participation in a study entail?

Each study is unique, but generally, participation involves clinic visits, completing health diaries, and occasional check-ins. Most studies are outpatient, so no overnight stays are required.

Am I eligible to join a clinical trial?

Eligibility varies by study. Contact our team, and we’ll help determine if there’s a trial that fits your health profile.

Who pays for clinical trials?

Our studies are funded by sponsors, so there are no costs to participants.

Will I be charged with any costs to participate?

No, participation is free, and compensation is provided to eligible participants.

What should I think about before joining a clinical trial?

Consider asking questions like:
1-Who will be my primary contact?
2-What is the study’s purpose?
3-Has the treatment been tested before?
4-What tests or procedures are involved?
5-Will this impact my daily routine?

Will I ever find out if I got the placebo?

This depends on the study. Some trials reveal whether participants received the placebo after completion, known as "breaking the blind." Our team will inform you if this is an option.

Stay Informed

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