Enrolling Studies at Our Four Locations

Click to view enrolling studies at each location:

Portsmouth

Portsmouth, NH

110 Corporate Drive,
Suite #2, Portsmouth NH 03801

Beverly, MA clinical research trial study studies ActiveMed Portsmouth NH Beverly MA Methuen MA

Beverly, MA

138 Conant St,
1st Floor Beverly, MA 01915

Methuen, MA clinical research trial study studies ActiveMed Portsmouth NH Beverly MA Methuen MA

Methuen, MA

421 Merrimack Street,
Suite 203 Methuen, MA 01844

New England Neurology Associates at Riverwalk

Lawrence, MA (Riverwalk)

354 Merrimack St.
Lawrence, MA 01843

Enrolling Studies ActivMed Clinical Research Trials

Participate in Clinical Research?

Clinical research studies can be a great opportunity for people to receive medical services at no cost and to learn more about their medical condition. Volunteers in medical research studies, in most cases, are compensated for their time and travel commitments in the form of a stipend. At ActivMed, we ensure volunteering is a positive experience for every participant. Our friendly staff understands and recognizes that all participants in medical studies are volunteers; therefore, we respect every participant’s time and commitment. In addition to compensation, volunteers often receive diagnostic testing and careful evaluation by a board-certified medical doctor. Lastly, many volunteers find that participation in medical studies can be a great learning experience that allows them to have a better understanding of their medical condition and potential treatment options. Participation is always voluntary and participants can choose to withdraw from a study at any time. Every medical study has different requirements, procedures, risks and benefits. See our list of enrolling study opportunities and call or apply today. Our friendly staff will gladly explain the details of study participation over the phone or by email.

Frequently Asked Questions (FAQ’s)

What is a clinical research trial?

A clinical research trial is a necessary step when pharmaceutical companies want to evaluate a new medication, device, or procedure. New medications, prescription or over the counter (OTC), must be tested thoroughly before being approved by the Federal Drug Administration (FDA). A clinical trial is designed to study the safety and effectiveness of a product, under the strict guidelines of the FDA.

Trials are conducted in four phases:

  • Phase I is conducted on a small number (tens) of volunteers to test how the drug is absorbed, metabolized, and excreted in the human body.
  • Phase II (few hundred) focus on how the drug compares to existing drugs or in general.
  • Phase III (few thousand) continues to study the effectiveness of the drug over several years. After this phase, pharmaceuticals can submit the data to request FDA approval.
  • Phase IV trials are conducted after the FDA has approved the medications for consumer sale. These studies focus on long-term effectiveness, cost effectiveness of the medicine, and can later be removed from the market, or safety warnings added to the labeling, based on study findings.

Each study follows a strict protocol that outlines who can participate, how much medication will be given, and how the effects will be measured. Each clinical trial is overseen by a Principal Investigator- a medical doctor trained in clinical research. At ActivMed, all our Principal Investigators that work with us are Board Certified, and have patients in their own practices.

Why should I participate?

People choose to participate in clinical research for a variety of reasons. Some people choose to participate to have access to new treatments, if their current treatments are not working. Some people choose to participate to help advance medical knowledge. Participants also benefit from receiving a great level of medical care from diagnostic testing, free medications, and one-on-one physician consultations. Volunteers are also compensated for their travel and time, in the form of a stipend.

All volunteers are evaluated as part of a screening process, to determine study eligibility. Protocols have strict criteria as to who can be included in a study. The screening process may include: diagnostic testing, blood draws, questionnaires, vital signs, physical exams, etc. Participants are always given all the information they need to make a decision regarding a study, and can choose to withdraw at any time. This is done through an informed consent process.

What is informed consent?

Before consenting to participate in a study, the FDA requires the patient to sign the Informed Consent document, stating that they understand the risks, expectations, time commitments, and compensations for a trial. An Informed Consent form is a step-by-step walkthrough of everything that will happen over the course of the clinical trial. This is a one-on-one conversation where you may ask questions, and have anything that you are uncomfortable with explained. Before signing an Informed Consent document, make sure you feel fully informed about the study, and are willing to accept all the requirements. A participant can withdraw from a study at any time, but may not be fully compensated.

This process isn’t the only time to ask questions. Please feel free to keep asking questions. We are here to help you!

How do I Know It’s Safe?

The Informed Consent process, is the first step in protecting our participants. This process is to provide you with all the information you need to weight the risks and benefits of participating in a study. Also, the FDA requires that all drugs, medical devices, or biological product be reviewed by International Review Boards (IRBs). An IRB is an individual ethics committee made up of doctors, researchers, and members of the community. The IRB’s approve the Informed Consent Documents and Protocols for all clinical trials, to ensure the study is ethical, and the rights and welfare of the patients are protected.

What about my personal information?

Your personal information is protected under HIPAA Privacy Rules, much in the same way as when you see your regular doctor. Researchers can obtain, create, and use your health information with your authorization, sharing it only with those involved in the clinical trial, and never disclosing enrollment in a study, or identifying participants in any reports of the research.

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Beverly, MA

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Methuen, MA

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Portsmouth, NH

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Lawrence, MA

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