MyPaTH Story Booth 2.0
Interested in sharing your story about health, illness, or research? Patients and caregivers are needed to participate in a research study to help learn more about topics that are important to you and that may improve health and health care. Participation involves one 45-minute session that takes place over the phone. Eligible participants must be able to read and understand English.
MyPaTH Story Booth – COVID-19 Stories
Participants are invited to share how they are maintaining their health during the coronavirus pandemic, or to share what it is like being ill with COVID-19 and/or caring for a loved one who is ill with COVID-19. Participation in this research study involves one 45-minute session that takes place over the phone. Eligible participants must be able to read and understand English.
Improving Pain Management and Opioid Safety for Patients with Cirrhosis
Have you been diagnosed with cirrhosis, and have you been living with chronic pain? You may be able to participate in a study that will evaluate the use of a health education program for patients with cirrhosis. Compensation is provided.
All of Us Pennsylvania Research Program
You may be able to change the future of medicine. The All of Us PA Research Program is enrolling adults 18 years of age or older. This may be your chance to improve how your children and your children’s children receive medical care.
Genetics of Inflammatory Bowel Disease – Healthy Volunteers
Are you a healthy, white individual between the ages of 18 and 35? If so, you may be eligible to help researchers understand the genetics of inflammatory bowel disease (IBD). Researchers hope to identify IBD-causing genes, which determine a person’s make-up and inherited traits. Involves one study visit, participants will be asked to give approximately 4 tbsp. of blood. Compensation provided.
IBD Research Registry
Are you 18 years of age or older, and are seeking or already receiving treatment at the UPMC Inflammatory Bowel Disease Center? If so, you may be able to take part in the IBD Research Registry, which is a list of individuals who are interested in having their medical information included in research studies and being contacted about future research studies.