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An Educational Intervention on Provider Knowledge for the Support of Cancer Survivors

Survivorship ECHO Project

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06062901
Enrollment
28
Registered
2023-10-02
Start date
2021-09-17
Completion date
2023-09-19
Last updated
2025-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematopoietic and Lymphoid Cell Neoplasm, Malignant Solid Neoplasm

Brief summary

This clinical trial utilizes the Project Extension for Community Healthcare Outcomes (ECHO) model to recruit, train, and support community healthcare providers in cancer survivorship best practices. Cancer survivors have distinct medical needs and are more likely to report being in poor or fair overall health compared to those who do not report a history of cancer. There is a lack of educational opportunities focused on survivorship care for health providers. Although progress has been made with the development of survivorship guidelines, physicians continue to express barriers to addressing concerns of cancer survivors. This study is to utilize a Survivorship ECHO education intervention to assess its effects on provider knowledge and comfort with survivorship guidelines as well as greater adherence to guideline concordant breast cancer survivorship care recommendations.

Detailed description

PRIMARY OBJECTIVES: I. Determine the effectiveness of the Survivorship ECHO's platform by assessing provider knowledge of cancer survivorship best practices using pre- and post-enrollment surveys. II. Evaluate implementation of survivorship best practices into clinical practice and documentation after enrollment in our Survivorship ECHO. OUTLINE: Participants attend 6 sessions of Survivorship ECHO educational intervention over 1 hour each, every 2 weeks for 12 weeks. Participants may optionally participate in a one-on-one interview to give feedback about the sessions over 30 minutes.

Interventions

OTHEREducational Intervention

Receive educational intervention

OTHERInterview

Participate in one-on-one interview

OTHERSurvey Administration

Ancillary studies

Sponsors

Ohio State University Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Providers from The James Cancer Network (consists of five community sites in Ohio: St. Rita's Memorial Center, Memorial Health, Madison Health, Wooster Community Hospital, and Clinton Memorial Hospital) * Eligible participants will include registered nurses, advanced practice registered nurses, physician assistants, nutritionists, radiation oncologists and oncologists

Design outcomes

Primary

MeasureTime frameDescription
Change in level of understanding in key survivorship knowledge areasBaseline up to study completion, typically 1 yearIncludes knowledge on surveillance, late and long-term effects of chemotherapy, health promotion, disease prevention and psychosocial evaluation and support. A Likert survey will assess provider comfort and knowledge with core cancer survivorship competencies with higher scores associated with higher levels of knowledge and comfort.
Met and unmet needsUp to study completion, typically 1 yearContent, participant needs, and aspects of delivering the Survivorship ECHO platform explored using qualitative analysis.
Acceptability of current structureUp to study completion, typically 1 yearContent, participant needs, and aspects of delivering the Survivorship ECHO platform explored using qualitative analysis.
Barriers to accessing ECHOUp to study completion, typically 1 yearContent, participant needs, and aspects of delivering the Survivorship ECHO platform explored using qualitative analysis.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026