Research Opportunity for Adults Using the Orencia® Autoinjector

Participants with Orencia® autoinjector experience are needed for a patient usability study.

Sample Clinical Trial hero

Condition

Psoriatic Arthritis and Rheumatoid Arthritis

Overview

This patient usability study is for adults in the United States with Psoriatic Arthritis or Rheumatoid Arthritis who currently use, or have used within the last 6 months, the Orencia® (abatacept) autoinjector. The study will help researchers understand real patient needs and device experience as future autoinjector device options are explored.

What will participants be asked to do?

  • Attend a one-time, 60-minute in-person study visit
  • Simulate use of demonstration autoinjector devices on an injection pad
  • Provide feedback on device design, handling, ease of use, and overall experience
  • No medication or treatment will be administered during this usability session

Participation Eligibility

You may be eligible to participate if you:

  • Are 18 years of age or older
  • Live in the United States
  • Have been diagnosed with Psoriatic Arthritis or Rheumatoid Arthritis
  • Currently self-administer, or have self-administered within the last 6 months, the Orencia® (abatacept) autoinjector

You may NOT be eligible to participate if you:

  • Have taken part in a research study about injection devices within the past 3 months
  • Work in market research, advertising, or a pharmaceutical company, or live with someone who works in one of those fields
  • Have worked within the last 10 years as a healthcare provider who gives injections as part of their job
  • Have vision, hearing, or hand/grip difficulties that would prevent them from completing medical tasks independently

 

Additional Information

Participants who complete the 60-minute in-person visit will receive a $300 stipend in appreciation of their time and effort. Participation is completely voluntary.

The study team will review eligibility and provide study visit details before participation.

Privacy: Your information will not be shared with other parties without your permission.

Disclaimer: Orencia® is a registered trademark of Bristol Myers Squibb (BMS). This study is not sponsored by, affiliated with, or endorsed by BMS.

For More Information

Click here for the patient information flyer.

Learn more and see if you pre-qualify by visiting the link or scanning the QR code.

Orencia QR Code

Contact Information

For questions, contact us at oruschi_study_recruiting@nemara.net or call (781)-296-3678.

Study Sponsor

Nemera