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EAQ202, Improving Adolescent and Young Adult Self-Reported Data in ECOG-ACRIN Trials

All genders
person-wave 18-39
Recruiting now
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Principal Investigator: Susan Parsons, MD

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

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Latoya Lashley

Study details

Inclusion Criteria
  • 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.
Exclusion Criteria
  • Patient must not have a recurrence or second primary cancer. Patients must not have basal cell skin carcinoma.
Study Requirements

A pilot randomized controlled trial with AYAs to determine the feasibility and acceptability of completing PROs informed by AYAs' priorities. AYAs will be consented and randomized to select five HRQOL domains from a dashboard (Choice PRO) at each assessment period or to five standard HRQOL domains (Fixed PRO; physical function, pain, cognitive function, social support, finances) at each assessment period. AYAs will complete baseline, 1-, 3-, 6-, and 12-month assessments which will include a combination of CATs and static short forms.

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