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EAQ202

Improving Adolescent and Young Adult Self-Reported Data in ECOG-ACRIN Trials

View on ClinicalTrials.gov

Quick Information

Age Group
Adult (18-64)
Sex/Gender
All Genders
Accepts Health Volunteers
No
Phase
NA
Offered at
Gundersen Lutheran Medical Center
Condition(s)
  • 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
Protocol Number
NCT05108298

Summary

The purpose of this study is to evaluate feasibility and acceptability of completing PROs among AYAs randomized to Choice PRO vs Fixed PRO.

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 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.

Exclusion Criteria:

Patient must not have a recurrence or second primary cancer. Patients must not have basal cell skin carcinoma.

View on ClinicalTrials.gov

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La Crosse, WI 54601

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