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

Recruiting now · Not applicable

Conditions studied: 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

In brief

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

Key facts

Study ID

NCT05108298

Run by

Eastern Cooperative Oncology Group

People needed

400

Starts

2021-11-10

Expected to finish

2027-05-01

Last updated by the study team

2026-07-17

Who can join

Age: 18 and older, up to 39. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

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

Where it is running

• Wellmont Holston Valley Hospital and Medical Center — Kingsport, Tennessee, United States (enrolling)
• Bristol Regional Medical Center — Bristol, Tennessee, United States (enrolling)
• Cancer Center at Saint Joseph's — Phoenix, Arizona, United States
• CHI Saint Vincent Cancer Center Hot Springs — Hot Springs, Arkansas, United States
• CARTI Cancer Center — Little Rock, Arkansas, United States
• Mission Hope Medical Oncology - Arroyo Grande — Arroyo Grande, California, United States
• Mercy Cancer Center - Carmichael — Carmichael, California, United States
• Bay Area Tumor Institute — Oakland, California, United States
• Mercy San Juan Medical Center — Carmichael, California, United States
• Epic Care-Dublin — Dublin, California, United States
• Mercy Cancer Center - Elk Grove — Elk Grove, California, United States
• Bay Area Breast Surgeons Inc — Emeryville, California, United States
• Epic Care Partners in Cancer Care — Emeryville, California, United States
• Contra Costa Regional Medical Center — Martinez, California, United States
• Mercy Cancer Center — Merced, California, United States
• PCR Oncology — Arroyo Grande, California, United States
• Mercy Cancer Center - Rocklin — Rocklin, California, United States
• Mercy Cancer Center - Sacramento — Sacramento, California, United States
• Pacific Central Coast Health Center-San Luis Obispo — San Luis Obispo, California, United States
• Mission Hope Medical Oncology - Santa Maria — Santa Maria, California, United States
• Epic Care Cyberknife Center — Walnut Creek, California, United States
• Woodland Memorial Hospital — Woodland, California, United States
• Rocky Mountain Cancer Centers-Aurora — Aurora, Colorado, United States
• The Medical Center of Aurora — Aurora, Colorado, United States
• Mercy Hospital Fort Smith — Fort Smith, Arkansas, United States

Full record on ClinicalTrials.gov

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