For Patients & Volunteers
Participating in Clinical Research
Clinical trials are essential for developing new treatments and improving healthcare. By participating in a clinical trial, you can help advance medical knowledge while potentially gaining access to innovative treatments.
Why Participate in Clinical Trials?
Access to Innovative Treatments: Opportunity to receive cutting-edge therapies before they're widely available
Comprehensive Care: Regular health monitoring by specialized medical professionals
Contribution to Medical Advancement: Help develop treatments that may benefit others with similar conditions
Community Involvement: Participate in research that takes place within your local community
Convenience: Our community-based and mobile approaches make participation more accessible
Compensation: Many studies provide compensation for time and travel expenses
Our Patient-Centric Approach
Community-Based Research
Our clinical trials take place in local healthcare settings, making participation more convenient and comfortable.
Mobile Clinical Trials
Many of our studies include home visits or remote elements, reducing the need for frequent travel to research sites.
Experienced Research Teams
Our staff are specially trained in clinical research and dedicated to providing high-quality care.
Clear Communication
We ensure you understand all aspects of the study, including potential risks and benefits, before you decide to participate.
Patient Safety
Your safety is our top priority, with comprehensive monitoring throughout the study.
Diversity & Inclusion
We're committed to ensuring clinical trials include diverse populations to develop treatments that work for everyone.
The Clinical Trial Process
Initial Contact
Reach out to us through our website, phone, or referral from your healthcare provider to express interest in participating.
Pre-Screening
A brief phone conversation to determine if you might be eligible for any current or upcoming studies.
Informed Consent
Detailed information about the study is provided, and you'll have the opportunity to ask questions before deciding to participate.
Screening Visit
Medical evaluations to determine if you meet all criteria for the study.
Study Participation
Regular visits for treatment administration, monitoring, and assessments according to the study protocol.
Study Completion
Final assessments and follow-up care as needed.
Current Research Areas
Psychiatry Studies
We conduct clinical trials in various psychiatric conditions, including:
Autism Spectrum Disorder
ADHD
Depression
Anxiety Disorders
Bipolar Disorder
Schizophrenia
PTSD
Vaccine Studies
Our vaccine clinical trials include:
Preventive Vaccines
Therapeutic Vaccines
Pediatric Vaccines
Adult Vaccines
Infectious Disease Vaccines
We also conduct studies in neurology, pediatrics, rare diseases, immunology, and infectious diseases.
Patient Testimonial
“Participating in a clinical trial through DSP Vigilance Group was a positive experience. The research team was caring and professional, and I appreciated being able to receive study visits at home, which made it much easier to participate with my busy schedule."
- Maria R., Clinical Trial Participant.”
Frequently Asked Questions
What is a clinical trial?
A clinical trial is a research study that evaluates the safety and effectiveness of new medical treatments, devices, or approaches. These studies help determine if new treatments work and are safe before they become widely available.
Who can participate in clinical trials?
Each clinical trial has specific eligibility criteria based on factors such as age, gender, type and stage of disease, previous treatment history, and other medical conditions. These criteria help ensure that the study results will be clear and meaningful.
What are the benefits of participating?
Potential benefits include access to new treatments before they're widely available, expert medical care, and the opportunity to play an active role in your healthcare. You'll also be contributing to medical knowledge that may help others in the future.
Are there risks involved?
All clinical trials have potential risks, which may include side effects from treatments, time commitments, or treatments that may not work for you. The research team will explain all potential risks during the informed consent process.
What is informed consent?
Informed consent is the process of learning the key facts about a clinical trial before deciding whether to participate. It includes details about the study's purpose, duration, required procedures, and key contacts. Potential risks and benefits are explained in the informed consent document.
Can I leave a study after it begins?
Yes, you can leave a clinical trial at any time for any reason. When withdrawing from a trial, you should let the research team know about your decision and the reasons for it.
Interested in Participating?
Contact us today to learn about current clinical trial opportunities or to join our database for future studies.