Improving Adolescent and Young Adult Self-Reported Data in ECOG-ACRIN Trials
Overview
Overview
The purpose of this study is to evaluate feasibility and acceptability of completing PROs among AYAs randomized to Choice PRO vs Fixed PRO.
Key Inclusion Criteria
Key Inclusion Criteria
For a patient to be eligible for participation in this study, all of the following criteria must apply.
- Patient must be ≥ 18 years and ≤ 39 years of age at registration. Patient must have a histologically confirmed diagnosis of primary cancer of any stage within 12 weeks (84 days) at registration.
- Patient must have received, be currently receiving or planning to receive treatment for cancer, including surgery and/or chemotherapy and/or radiation therapy.
- Patient must have an ECOG performance status 0-3.
- Patient must have a life expectancy >24 months.
- Patient must be able to complete questionnaires in English.
- Patient must have internet access through computer, tablet, or smartphone.
- Patient must have an email address.
- Patient must have a mobile phone able with text messaging capabilities.
- Patient must be able to accurately provide self-report data (e.g. per clinical judgment, cognitive function is intact).
- Patient must be able to provide informed consent
Key Exclusion Criteria
Key Exclusion Criteria
A patient will not be eligible for participation in this study if any of the following criteria apply.
- Patient must not have a recurrence or second primary cancer. Patients must not have basal cell skin carcinoma.
Learn More
Learn More
To learn more, visit ClinicalTrials.Gov
Study Type
Observational
Principal Investigator(s)
Jeremy Kilburn, MD
Sponsor(s)
Eastern Cooperative Oncology Group
Contact Us
Contact Us
To participate in this study, please contact Clinical Research at
864-560-6812