KanSurvive: Testing a Model for Improving Cancer Survivorship Care in Rural Practice
Completed · Not applicable
Conditions studied: Breast Cancer, Colorectal Cancer, Lung Cancer, Prostate Cancer
In brief
Approximately, 20 rural primary care practices to participate in a delayed intervention-controlled trial. Phase I: Formal and structured work flow evaluations to better identify specific gaps in processes of care while assessing what on-going training is needed for adoption of high-quality cancer survivorship care in rural practice. These will be incorporated into the ECHO sessions (Aim 1). Phase II: Conduct and test the effectiveness of the novel KanSurvive-ECHO intervention (Aim 2) and finally identify barriers and facilitators to implementation of KanSurvive-ECHO (Aim 3).
Key facts
- Study ID
- NCT04763824
- Run by
- University of Kansas Medical Center
- People needed
- 15
- Starts
- 2020-11-18
- Expected to finish
- 2023-12-18
- Last updated by the study team
- 2026-01-14
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Primary care practice (PCP) caring for rural cancer survivors
- Willing to participate in four ECHO sessions
- Capable and willing to complete pre- and post- data collection under a data use agreement
- Cancer survivor data is eligible for extraction if the patient is a breast, prostate, lung, and/or colorectal cancer survivor and considered to have a "reasonable likelihood" of 24-month survival by a practice provider.
You may not qualify if…
- PCPs unwilling to engage in project activities
- PCPs with no rural-dwelling patients on their patient panel
- Cancer survivor data is ineligible for extraction if the patient is <18 years of age or >75 years of age, is currently receiving hospice services, or has a history of cancer other than breast, prostate, lung, or colorectal.
Where it is running
- University of Kansas Cancer Center — Westwood, Kansas, United States
Full record on ClinicalTrials.gov
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