NCT07528963

Brief Summary

Rural cancer survivors experience a higher risk of negative health outcomes and require coordinated care to address the many effects of cancer and its treatment. Primary care providers recognize the importance of providing high-quality, evidence-based survivorship care and are well-positioned to meet survivor needs, however, these needs are often unmet due to limitations in knowledge, lack of resources, and administrative demands. Practical strategies are needed to help PCPs improve cancer survivorship care, and this proposal will test implementation strategies to optimize the adoption of evidence-based practices for cancer survivorship care in rural primary care settings.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
36mo left

Started Jun 2025

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress27%
Jun 2025Jun 2029

First Submitted

Initial submission to the registry

April 15, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

June 30, 2025

Completed
10 months until next milestone

First Posted

Study publicly available on registry

April 14, 2026

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2028

Expected
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2029

Last Updated

June 18, 2026

Status Verified

June 1, 2026

Enrollment Period

3.1 years

First QC Date

April 15, 2025

Last Update Submit

June 16, 2026

Conditions

Keywords

cancer survivorshipprimary care practice

Outcome Measures

Primary Outcomes (1)

  • Provider Adherence to Cancer Survivorship Guidelines Measured by EHR-Based Composite Adherence Score

    The primary outcome is provider adherence to evidence-based cancer survivorship guidelines, measured using a composite score derived from electronic health record (EHR) data abstraction. The composite score assesses concordance between documented care and National Comprehensive Cancer Network (NCCN) survivorship guidelines across multiple domains (e.g., tumor surveillance, distress screening, BMI assessment, tobacco use screening, family history of cancer documentation, osteoporosis screening, and hereditary cancer risk assessment). Scores are calculated based on the proportion of eligible guideline-concordant care processes completed for each patient and aggregated at the clinic level.

    Assessed at baseline, 6, 12, and 24 months

Study Arms (3)

Virtual Scribe Medical Assistant

ACTIVE COMPARATOR

Virtual scribe medical assistants will engage in KanSurvive 2.0 Project ECHO education assist with clinical documentation, identifying cancer survivors, and scrubbing electronic health records to identify care gaps and opportunities for quality improvement with practice facilitation.

Other: KanSurvive telementoring and educationOther: Practice facilitation for quality improvementOther: Survivorship Care ManualOther: Virtual scribe services

Team Based Care

ACTIVE COMPARATOR

Rural primary care practice teams will assist with clinical documentation, identifying cancer survivors, and reviewing electronic health records to identify care gaps and opportunities for quality improvement with practice facilitation.

Other: KanSurvive telementoring and educationOther: Practice facilitation for quality improvementOther: Survivorship Care Manual

Enhanced Usual Care

PLACEBO COMPARATOR

This attention control arm will engage in KanSurvive 2.0 Project ECHO education and receive an obesity management toolkit.

Other: KanSurvive telementoring and educationOther: Obesity management toolkitOther: Survivorship Care Manual

Interventions

Telementoring, education, and case-based learning covering evidence-based practice guidelines for breast, colorectal, lung, and prostate cancer survivorship.

Enhanced Usual CareTeam Based CareVirtual Scribe Medical Assistant

Practice facilitation will be delivered to assist with quality improvement efforts using monthly Plan Do Study Act (PDSA) cycles.

Team Based CareVirtual Scribe Medical Assistant

Printed and digital manuals will be distributed to each participating primary care practice to share with the cancer survivors they see in their clinic. The manual guides patients on how to engage more effectively with their PCP and oncology care team and reviews recommended follow-up, within a format of a "service manual" and written in lay language.

Enhanced Usual CareTeam Based CareVirtual Scribe Medical Assistant

Participating practices who opt-in to receive virtual scribe services.

Virtual Scribe Medical Assistant

The Enhanced Usual Care arm will receive a short, virtual training and toolkit on the management of obesity in primary care practice and how it relates to cancer survivorship.

Enhanced Usual Care

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Rural primary care practice (PCP) located within rural urban continuum codes (RUCC) 4-9 in Kansas
  • PCPs must have multiple providers
  • PCPs must have at least on medical assistant
  • PCPs must have an employed medical scribe or be willing to consider employing a medical scribe using study compensation and practice revenue
  • 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 not located within RUCC 4-9 in Kansas
  • PCPs without multiple providers
  • PCPs without a medical assistant
  • PCPs without a medical scribe or unwilling to consider employing one
  • Cancer survivorship data is ineligible for extraction is 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Kansas Medical Center

Kansas City, Kansas, 66160, United States

Location

MeSH Terms

Interventions

Educational StatusQuality Improvement

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation CharacteristicsEngineeringTechnology, Industry, and AgricultureQuality of Health CareHealth Services Administration

Study Officials

  • Allen K Greiner, MD, MPH

    University of Kansas Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: 8 rural primary care practices will be randomized to the Virtual Scribe Medical Assistant arm, 4 rural primary care practices will be randomized to the Team-Based Care arm, and 4 rural primary care practices will be randomized to the Enhanced Usual Care control arm.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 15, 2025

First Posted

April 14, 2026

Study Start

June 30, 2025

Primary Completion (Estimated)

August 1, 2028

Study Completion (Estimated)

June 30, 2029

Last Updated

June 18, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will share

Research resources generated within this project will be explicitly developed in an effort to improve cancer survivorship outcomes in rural primary care practice. We will develop a strategic plan with the KU Cancer Center and NCI to widely disseminate any product, intellectual property, or data to promote scientific activity and health promotion work that will be of assistance to similar patient populations. As such, we will work to fully share these materials and items with qualified individuals across the greater scientific community and with rural practices, providers and community members. All program materials and data generated within the overall study will be shared to the fullest extent possible. De-identified data from this project will be preserved and shared in a public repository to validate and replicate research findings described in the Aims.

Shared Documents
STUDY PROTOCOL, SAP
Time Frame
Start date: June 2026 End date: June 2029
Access Criteria
De-identified study data will be made available as public use data to the research community via Open Science Framework.

Locations