Navigation Interventions for Patients With Breast Cancer and High-risk Social Determinants of Health
From Screening to Action: Implementing Navigation Interventions for Patients With Breast Cancer and High-risk Social Determinants of Health
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
This study aims to assess how individual patient social stressors are associated with barriers to care by analyzing a patient navigator system. Patient navigators will connect patients with unmet social needs with community resources.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Eligibility Criteria: * Diagnosed with breast cancer (any stage). * Currently being treated for breast cancer by a breast medical oncologist at Siteman Cancer Center North County. This includes any treatment, PO or IV, including hormonal therapy. It does not include patients enrolled in clinical trials. * At least 18 years of age. * English-speaker. * Verbally consented to navigation services.
Study sites (1)
MO
- Washington University School of Medicine · St Louis, MO 63310Emily L Podany, MD, MPHS · Study contact · 314-273-4474 · elpodany@wustl.eduKatherine N Weilbaecher, MD · Study contact · 314-362-5654 · kweilbae@wustl.eduEmily L Podany, MD, MPHS · Principal investigatorBenjamin Bowe, PhD · Sub-investigatorMore trials in St Louis