About this trial

The purpose of the study is to characterize baseline multidisciplinary tumor board (MDTB) context and variability, evaluate the relationship between baseline fitness of patients with cancer and initial treatment recommendations, and assess the impact of the INSPIRE intervention, which involves including electronic patient reported outcomes (ePROs) within MDTB on MDTB discussion content, provider burden, treatment recommended and received, healthcare utilization, and patient-reported outcomes.

Eligibility criteria

Qualifiers

None

Disqualifiers

aged 18 years or older;

with suspected or confirmed diagnosis of pancreatic, breast, and gynecologic cancer (all stages) within 8 weeks of diagnosis;

intention to be treated at a participating institution;

with verbal fluency in English or Spanish; and

Trial design

Treatments tested in this trial

  • INSPIRE (INtegrating Systematic PatIent-Reported Evaluations)
  • Capture of patient-reported outcomes
  • Enhanced Clinician Awareness

Treatment groups

2,748 Participants
are divided into 3 treatment groups

Locations

3
University of Alabama at Birmingham35294, BirminghamAlabama, United States
University of California Los Angeles (UCLA)90404, Los AngelesCalifornia, United States
University of Oklahoma (OU) Health Campus73126-0901, Oklahoma CityOklahoma, United States

Sponsors and collaborators

University of Alabama at Birmingham

Lead sponsor

University of Oklahoma

Collaborator

University of California, Los Angeles

Collaborator

Canopy Cancer Collective, LLC

Collaborator