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

Eastern Cooperative Oncology Group
NCT IDNCT05108298ClinicalTrials.gov data as of Apr 2026
Target enrollment

400

Study length

about 5.5 years

Ages

18–39

Locations

347 sites in AK, AR, AZ +28

About this study

This trial is testing whether adolescents and young adults (AYAs) can complete questionnaires more easily if they choose which questions to answer, compared to answering standard questions. The goal is to see if this approach improves the amount of information collected from AYAs participating in cancer treatment trials.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Questionnaires
Primary goalEvaluate completion of PROs among AYAs randomized to Choice PRO vs Fixed PRO

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low6%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Evaluate completion of PROs among AYAs randomized to Choice PRO vs Fixed PRO.

Body systems

Oncology