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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Questionnaires

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

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

Body systems

Oncology