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The aim of this study was to evaluate the program\u2019s educational outcomes in its pilot year, using Moore\u2019s Evaluation Framework for Continuing Medical Education and focusing on the program\u2019s impact on participants\u2019 knowledge, confidence, and professional practice. We collected data in 22 semi-structured interviews (13 PCPs and 9 non-PCPs) and 30 anonymous one-time surveys (14 PCPs and 16 non-PCPs) from the program participants (hub and spoke site members), as well as from members of the target audience who did not participate. In the first year, average attendance at each session was 2.5 PCPs and 12 non-PCP professionals. In spite of a relatively low PCP participation, the program received very positive satisfaction scores, and participants reported improvements in knowledge, confidence, and practice. Both program participants and target audience respondents particularly valued three features of the program: its conversational format, the real-life experiences gained, and the support received from a professional interdisciplinary community. PCPs reported preferring case discussions over didactics<jats:italic>.<\/jats:italic> Our results suggest that the Cancer ECHO program has benefits over other PCP-targetted cancer control interventions and could be an effective educational means of improving cancer control capacity among PCPs and others. Further study is warranted to explain the discrepancies among study participants\u2019 perceptions of the program\u2019s strengths and the relatively low PCP participation before undertaking a full-scale effectiveness study.<\/jats:p>","DOI":"10.1186\/s12911-022-01874-x","type":"journal-article","created":{"date-parts":[[2022,5,17]],"date-time":"2022-05-17T12:15:59Z","timestamp":1652789759000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["An evaluation of an Extension for Community Healthcare Outcomes (ECHO) intervention in cancer prevention and survivorship care"],"prefix":"10.1186","volume":"22","author":[{"given":"Zheng Z.","family":"Milgrom","sequence":"first","affiliation":[]},{"given":"Tyler S.","family":"Severance","sequence":"additional","affiliation":[]},{"given":"Caitlin M.","family":"Scanlon","sequence":"additional","affiliation":[]},{"given":"Any\u00e9 T.","family":"Carson","sequence":"additional","affiliation":[]},{"given":"Andrea D.","family":"Janota","sequence":"additional","affiliation":[]},{"given":"Terry A.","family":"Vik","sequence":"additional","affiliation":[]},{"given":"Joan M.","family":"Duwve","sequence":"additional","affiliation":[]},{"given":"Brian E.","family":"Dixon","sequence":"additional","affiliation":[]},{"given":"Eneida A.","family":"Mendonca","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[2022,5,17]]},"reference":[{"unstructured":"Indiana Cancer Consortium. 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Participation was voluntary, and the participants responded to the study invitation via emails and confirmed their interest. Informed consent was obtained from all participants. A written Study Information Sheet was given to the participants at the begginging of the survey and before the interviews. Verbal consent was confirmed again at the beginning of the interviews. The participants had the right to withdraw from the study without affecting their ability to participate in the Cancer ECHO program at anytime without prejudice. All methods were performed in accordance with the relevant guidelines and regulations.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"I declare that the authors have no competing interests as defined by BMC, or other interests that might be perceived to influence the results and\/or discussion reported in this paper.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"135"}}