Transforming patient care through clinical research

FAQs

What does participation in a clinical trial involve?

Participation in a clinical trial involves conducting research studies with patients who meet specific eligibility criteria. As a provider, your role is to identify potential candidates from your practice and offer them access to investigational treatments that may not yet be widely available. Profound Research manages all regulatory, administrative, and logistical aspects of the trial, allowing you to focus on patient care.

Patients who choose to participate will receive detailed information about the study, including potential risks and benefits. They will undergo screenings, follow a structured protocol, and receive regular medical evaluations throughout the trial.

Who can take part in a clinical trial?

Eligibility for clinical trials varies depending on the study’s objectives, but in general, participants must meet specific medical, demographic, and lifestyle criteria. This can include factors such as age, medical history, current health status, and previous treatments.

As a provider, your role is to help determine whether a patient qualifies for a trial and discuss whether participation aligns with their healthcare goals. Profound Research provides comprehensive eligibility screening support to ensure appropriate patient selection.

What are clinical trials, and why are they done?

Clinical trials are research studies designed to evaluate new medical treatments, drugs, devices, or procedures. These studies help determine the safety, effectiveness, and potential side effects of investigational therapies before they are approved for widespread use.

Clinical trials are essential for advancing medicine, improving patient outcomes, and offering new therapeutic options for conditions that may not have effective treatments. By participating in research, providers contribute to medical innovation while offering their patients access to cutting-edge care.

Are there any benefits or risks to participating?

Yes. Clinical trial participation can offer several benefits, including:

• Access to advanced treatments before they become widely available.
• Close monitoring and comprehensive care from experienced clinical research professionals.
• The opportunity to contribute to medical advancements that may benefit future patients.

However, there are also risks to consider:

• Potential side effects or adverse reactions from investigational treatments.
• The possibility that the treatment may not be more effective than existing standard therapies.
• Time commitments for study visits, monitoring, and follow-ups.

Profound Research prioritizes patient safety, ensuring that all trials adhere to strict ethical and regulatory standards. We provide full transparency regarding potential risks and benefits to help providers and patients make informed decisions.

How does Profound Research support providers in clinical trial participation?

Profound Research acts as an extension of your practice, handling all operational aspects of the trial so that you can focus on patient care.

We provide:

• Turnkey trial management, including study setup, patient recruitment, and compliance.
• Dedicated research coordinators who guide your team and patients through the process.
• Regulatory and administrative support, ensuring adherence to FDA and IRB requirements.
• Data collection and reporting, minimizing the burden on your practice while maximizing efficiency.

Our goal is to integrate research seamlessly into your workflow, allowing you to enhance patient care without additional administrative strain.

How can I get started with Profound Research?

Getting started is simple. If you’re interested in integrating clinical trials into your practice, Profound Research will guide you through every step. The process includes:

1. Initial consultation – We assess your practice’s suitability for research and discuss available studies.
2. Site qualification – Our team ensures your site meets regulatory requirements.
3. Study onboarding – We provide training and support to align with trial protocols.
4. Ongoing collaboration – Our research coordinators work alongside your team to facilitate patient recruitment and study execution.

If you’re ready to explore how clinical research can benefit your patients and practice, contact us to learn more about available opportunities. Link to contact page/form.