No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
2,748 (estimated)
Sponsor
University of Alabama at Birmingham · Other
Who this trial is looking for
This trial is looking for adults with certain types of cancer to improve how treatment options are discussed by doctors. Participants will share their treatment experiences and help doctors make recommendations based on patient feedback.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I have been diagnosed with pancreatic, breast, or gynecologic cancer within the last 8 weeks
I plan to receive treatment at a participating hospital
I can speak English or Spanish
I am scheduled to be discussed at a tumor board meeting
You may not be able to join if
I plan to receive cancer treatment outside the participating hospital
I cannot speak English or Spanish
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 b…
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.
Trial Locations
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Eligibility Criteria
Inclusion/Exclusion Criteria: We will include two populations: (1) patients and (2) clinical team members involved in the MDTB.
Inclusion Criteria:
* Inclusions Criteria- Patients:
1. aged 18 years or older;
2. with suspected or confirmed diagnosis of pancreatic, breast, and gynecologic cance…
Inclusion/Exclusion Criteria: We will include two populations: (1) patients and (2) clinical team members involved in the MDTB.
Inclusion Criteria:
* Inclusions Criteria- Patients:
1. aged 18 years or older;
2. with suspected or confirmed diagnosis of pancreatic, breast, and gynecologic cancer (all stages) within 8 weeks of diagnosis;
3. intention to be treated at a participating institution;
4. with verbal fluency in English or Spanish; and
5. scheduled to be discussed at MDTB.
* Inclusion criteria - Clinicians:
All clinical team members participating in the pancreatic, breast, or gynecologic MDTB at a participating site will be included and have pre-emptively agreed to participation.
Exclusion Criteria:
* Exclusion criteria - Patients:
Individuals with plans to receive cancer treatment outside the participating institution and inability to speak English or Spanish.
* Exclusion criteria - Clinician:
Clinicians will retain the opportunity to opt-out of participation, in which case their portions of the discussion will not be included in the analysis; however, this is not anticipated based on pilot data.
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