Evaluating the Communication Between Patients and Providers in Cancer Clinics
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: TrialTalk™.
- Who it may be relevant to
- Registry conditions: Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Evaluating the Impact of TrialTalkTM; to Foster Equitable Cancer Care
Overview
This clinical trial seeks to understand patients' experiences with the healthcare team and the quality of communication between patients and doctors in cancer clinics. The main question it aims to answer is: * Does TrialTalk™ improve communication between providers and patients? Participants will complete questionnaires before and after their standard of care clinic visit.
Detailed description
The online TrialTalk™ training system uses evidence-based principles and best practices for instructional design for adult learners. The system uses a four-stage learning goal framework (i.e., knowledge, skill, understanding, and application) to ensure that the training moves from rote knowledge- and skill acquisition to integration, application, ownership, and long-term memory in clinical practice. The first module introduces the TrialTalk™ framework, why it's relevant and effective to patients and providers and describes the learning goals for the rest of the course. The second module focuses on essential elements of the TrialTalk™ conversation process through examples, metaphors, and description, followed by exercises at the end of the module that solidify the basic concepts of the conversational process. The third module focuses on the essential components of the diagram, how it integrates with the conversational process, and how to use it in a patient meeting. A set of assessment and reflection questions at the end of module 3 reinforces the concepts and components of the diagram. The fourth module brings all the TrialTalk™ elements together through case studies that exemplify how the conversational process and diagram work together in different types of patient meetings (for example, a new patient versus an established patient). Assessment and reflection questions at the end of module 4 focus on integrating and using the TrialTalk™ method in practice. Learners also develop a three-day action plan to begin to use TrialTalk™ with their patients. The TrialTalk™ training system provides learning resources to physicians such as a self-assessment rubric, FAQs, a checklist, and diagram template.
TrialTalk™ intervention includes two components: provider-focused skills-based training to ensure providers' competency in using the conversational and diagrammatic aspects of TrialTalk™, and the patient-facing component, which is the TrialTalk™ tool itself, to help patients understand their prognosis and treatment options in order to make a shared informed decision about their cancer management.
Interventions
- Other TrialTalk™
TrialTalk™ is a communication tool that focuses on making the options visible and accessible while involving patients in the discussion.
Primary outcome measures
- Fidelity - Providers [Time frame: Monthly for 6 months]
- Sustainability of TrialTalk™ communication tool [Time frame: 1 year]
- Change in quality of communication [Time frame: Up to 2 hours]
- Change in trust of provider [Time frame: Up to 2 hours]
- Usefulness of tool [Time frame: Up to 2 hours]
- Understanding of treatment options [Time frame: Up to 2 hours]
Eligibility criteria
Inclusion Criteria - Providers:
- Hematologists, medical oncologists, or hematology/oncology fellows
- Willing to complete TrialTalk™ training
Inclusion Criteria - Patients:
- ≥ 18 years old
- have a confirmed diagnosis of cancer
- identify as Black, African American, or non-Hispanic White
- can read and understand English to complete the study questionnaires
- had previous visits with the enrolled provider
Exclusion Criteria - Providers:
- providers who received previous training in the TrialTalk™ method or used it in practice before will be excluded
Exclusion Criteria - Patients:
\- have moderate to severe cognitive impairment as determined by participant's provider
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 3 centers
- Northwestern Memorial Hospital — Chicago
- Medical University of South Carolina — Charleston
- University of Wisconsin - Madison — Madison
Identifiers
NCT: NCT06985953 · 2025-0274 · A534260 · SMPH/MEDICINE/HEM-ONC · UW24152