Improving Adolescent and Young Adult Self-Reported Data in ECOG-ACRIN Trials
Recruiting
N/A
Interventional Study
Breast Cancer, NOS
CNS Primary Tumor, NOS
Cervical Cancer, NOS
Colorectal Cancer, NOS
Leukemia, NOS
Lymphoma, NOS
Miscellaneous Neoplasm, NOS
Non-Rhabdomyosarcoma Soft Tissue Sarcoma, NOS
Testicular Nonseminomatous Germ Cell Tumor, NOS
Thyroid Cancer, NOS
Melanoma
Bone Cancer, NOS
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 39
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 400 (estimated)
- Sponsor
- Eastern Cooperative Oncology Group · Research network
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About This Trial
The purpose of this study is to evaluate feasibility and acceptability of completing PROs among AYAs randomized to Choice PRO vs Fixed PRO.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
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…
Contacts
No contact information available.