Do you have Type 2 Diabetes?

Nicholas is just one of the more than 30 million Americans who live with diabetes.


“It’s a huge problem,” said Dr. Jeff Wayne, CTR’s Principal Investigator. “One of our roles at Headlands Research Sacramento and Lincoln (formerly known as Clinical Trials Research) is to fight this epidemic of diabetes. It’s just taking over this country.”


To participate in a Type 2 Diabetes study, please complete the "Get Started" form on this page, or contact us directly at (916) 434-8230. A staff member will contact you with details about our current studies. 

Get Started

Greater Sacramento, California Residents Only
Please fill out the form below and our friendly office staff will connect with you to see if you qualify for this study.

Located outside of California?
Please DO NOT fill out this form. Instead, please visit www.ClinicalTrials.gov to find a study near you. Thank you!



Authorization to Collect, Use, and Retain Health Information (Pre-Screening) By completing this registration, you authorize Clinical Trials Research to collect, use, and retain the personal and health information you provide to evaluate your eligibility for current and future research studies, maintain research pre-screening records, and, if permitted below, contact you about potential study opportunities. Your information may be shared with authorized research personnel, study sponsors, research partners, and regulatory authorities as necessary for these purposes. Reasonable safeguards are used to protect your information. You understand that you may not qualify for a study at this time, but your information may be retained and reviewed for future research opportunities. Your identifiable information will not be used in publications or public presentations. Your participation is voluntary. You may withdraw this authorization at any time by contacting Clinical Trials Research, (916) 434-8230, info@ctrsites.com. Upon withdrawal, no new uses or disclosures will occur, although information already used or disclosed may not be retrievable. Unless you withdraw your authorization, your information may be retained for an indefinite period for research pre-screening purposes.
Phone Contact Communications Consent
Email Communications Consent
Text Message (SMS) Consent
Acknowledgment and Signature By typing your name above, you acknowledge that you have read and understood the authorization above and are providing your electronic signature.

Seeking volunteers with Type 2 Diabetes

Thank you for considering participation in our Type 2 Diabetes study. After filling out the "Get Started" form, a member of our medical team will contact you to obtain more information, answer any questions you have and schedule an appointment for an office visit. In accordance with HIPAA regulations, your personal information will be maintained in strict confidence and will not be sold or used for any other purpose.

Study Length

Varies by study, we have many ongoing Diabetes studies available.

Qualifications

  • You have been diagnosed with Type 2 Diabetes
  • Additional criteria dependent upon applicable study

Benefits

Participants will receive the following at no cost: all study medication; study-related physical exams, EKG’s, and lab work.

Time & Travel

Compensation for time and travel is provided if you qualify.

Our Process

Step 1

Contact Us

Fill out the "Get Started" form above and submit your contact info to us and we will call you.

Step 2

Phone Screen

During a brief phone call, we will discuss your medical history, your medications and study details.

If you meet initial study requirements, we will schedule a convenient time to visit our office and meet with our study team.

Step 3

Office Visit

At your initial visit, you will be asked to complete a basic registration packet and read the study Informed Consent.

After signing the informed consent, we will perform study specific exams, procedures and lab tests.

View Registration Packet

Step 4

Begin Study

If your results meet the study criteria, you will be invited to complete the study.

Every study differs in the number of visits, timeline and potential compensation provided for time and travel. 

Your Study Coordinator and Investigator will provide all of the details and support you will need.