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N/A N=138 Health Services Research

KanSurvive: Testing a Model for Improving Cancer Survivorship Care in Rural Practice

Breast Cancer · Colorectal Cancer · Lung Cancer · Prostate Cancer

Enrolled (actual)
138
Serious AEs
Results posted
Jan 2026
Primary outcome: Primary: Tumor Surveillance Completion (Pre-Intervention) — 126 Participants — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
KanSurvive ECHO and Practice Facilitation (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Kansas Medical Center
Primary completion
Dec 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Tumor Surveillance Completion (Pre-Intervention)
126 <0.05 sig
PRIMARY
Tumor Surveillance Completion (Post-Intervention)
117
PRIMARY
Distress Screening Completion (Pre-Intervention)
116 <0.05 sig
PRIMARY
Distress Screening Completion (Post-Intervention)
116
PRIMARY
Body Mass Index (BMI) Assessment Completion (Pre-Intervention)
132 <0.05 sig
PRIMARY
Body Mass Index (BMI) Assessment Completion (Post-Intervention)
118
PRIMARY
Tobacco Use Screening Completion (Pre-Intervention)
115 <0.05 sig
PRIMARY
Tobacco Use Screening Completion (Post-Intervention)
119
PRIMARY
Cancer Diagnosis on Problem List (Pre-Intervention)
129 <0.05 sig
PRIMARY
Cancer Diagnosis on Problem List (Post-Intervention)
122
PRIMARY
Family History of Cancer Documentation (Pre-Intervention)
96 <0.05 sig
PRIMARY
Family History of Cancer Documentation (Post-Intervention)
115

Summary

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).

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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 75 years of age, is currently receiving hospice services, or has a history of cancer other than breast, prostate, lung, or colorectal.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04763824). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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