Published on in Vol 8 (2024)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/50931, first published .
Assessing Knowledge, Competence, and Performance Following Web-Based Education on Early Breast Cancer Management: Health Care Professional Questionnaire Study and Anonymized Patient Records Analysis

Assessing Knowledge, Competence, and Performance Following Web-Based Education on Early Breast Cancer Management: Health Care Professional Questionnaire Study and Anonymized Patient Records Analysis

Assessing Knowledge, Competence, and Performance Following Web-Based Education on Early Breast Cancer Management: Health Care Professional Questionnaire Study and Anonymized Patient Records Analysis

Original Paper

1Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria

2Department of Nursing, School of Medical and Life Sciences, Sunway University, Selangor, Malaysia

3Patricia Ritchie Centre for Cancer Care and Research, University of Sydney, Sydney, Australia

4Department of Surgery, National Taiwan University Hospital, Taipei City, Taiwan

5touch Independent Medical Education Limited, Stockport, United Kingdom

6Breast Center, Department of Obstetrics & Gynecology and Comprehensive Cancer Center Munich, University Hospital of Munich Ludwig Maximilian, Munich, Germany

7Latin American Cooperative Group and Oncoclínicas Group, Hospital São Lucas da Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil

Corresponding Author:

Michael Gnant, MD

Comprehensive Cancer Center

Medical University of Vienna

Spitalgasse 23

BT86/E01

Vienna, 1090

Austria

Phone: 43 1 40160 35602

Email: mgnant@icloud.com


Background: Web-based learning activities are key components of continuing medical education (CME) for health care professionals (HCPs). However, the published outcomes of web-based educational interventions for early breast cancer (EBC) are limited.

Objective: This study aims to objectively assess knowledge, competence, and performance among HCPs following participation in 2 EBC-focused CME activities and to identify the remaining educational gaps.

Methods: We developed 2 CME-accredited web-based educational activities addressing high-risk EBC, including integration of shared decision-making to optimize patient care (touchMDT) and stratification for early identification of high-risk patients and novel treatment strategies (touchPANEL DISCUSSION). Knowledge, competence, and performance were assessed before and after the activities against an expanded outcomes framework (levels 1-5) using self-reported questionnaires and an analysis of anonymized data extracted from patient records.

Results: Six months after the launch of the activity, 7047 and 8989 HCP participants engaged with touchMDT and touchPANEL DISCUSSION, respectively. The overall satisfaction was 82% (a total score of 20.6 out of 25) for the touchMDT and 88% (a total score of 21.9 out of 25) for the touchPANEL DISCUSSION. For the evaluation of knowledge and competence (50 respondents before the activity and 50 learners after the activity), there was a significant increase in the mean number of correctly answered questions from pre- to postactivity (touchMDT: median 4.0, IQR 3.0-5.0 to median 5.5, IQR 4.0-7.0; mean 4.00, SD 1.39 to mean 5.30, SD 1.56 and touchPANEL DISCUSSION: median 4.0, IQR 4.0-5.0 to median 6.0, IQR 5.0-7.0; mean 4.32, SD 1.30 to mean 5.88, SD 1.49; both P<.001). A significant improvement in self-reported performance (50 respondents before the activity and 50 learners after the activity) was observed in a combined analysis of both activities (median 3.0, IQR 2.0-3.0 to median 4.0, IQR 3.0-5.0; mean 2.82, SD 1.08 to mean 4.16, SD 1.45; P<.001). Patient record analysis (50 respondents before the activity and 50 learners after the activity) showed that the HCPs used a range of measures to determine EBC recurrence risk and revealed no significant differences in adjuvant therapies used before and after the activity (P=.97 and P>.99 for Ki-67 <20% and Ki-67 ≥20% tumors, respectively). The remaining educational gaps included strategies for implementing shared decision-making in clinical practice and the use of genetic and biomarker testing to guide treatment selection.

Conclusions: Brief, web-based CME activities on EBC were associated with an improvement in HCP knowledge, competence, and self-reported performance and can help identify unmet needs to inform the design of future CME activities.

JMIR Form Res 2024;8:e50931

doi:10.2196/50931

Keywords



Clinical Decision-Making in High-Risk Early Breast Cancer

Clinical decision-making in cancer can be complex, requiring health care professionals (HCPs) to consider multiple clinical factors, patient preferences, and environmental factors [1-3]. A multidisciplinary team approach can improve the overall quality of decision-making [4-7], and there is evidence that shared decision-making (SDM) with patients can lead to better adherence to treatment and outcomes [1,8,9]. However, obstacles such as lack of resource availability and patient factors (eg, cultures and health literacy) have prevented the complete integration of SDM into cancer care [1,10-14]. HCPs need to understand these obstacles to deliver high-level care tailored to the individual.

The complexity of treating high-risk early breast cancer (EBC) has increased further with the emergence of complex new data on risk stratification and treatment. These include data on the prognostic and predictive value of biomarkers and the benefits of cyclin-dependent kinase 4 and 6 inhibitors, second-generation selective estrogen receptor antagonists and degraders, and protein kinase B (Akt) inhibitors [15-20]. Furthermore, the guidelines on the management of EBC have been updated recently to reflect recent data, which can be interpreted as influencing clinical practice [5,21-28]. Because of this rapid influx of complex information, HCPs who treat EBC are challenged to keep up with practice changes; consequently, it can take time for new and emerging data to be effectively integrated into practice, and patients with EBC may not receive optimal care [29-32].

Effectiveness of Web-Based HCP Education in Breast Cancer

Effective continuing medical education (CME) programs are crucial to ensure that HCPs implement up-to-date, evidence-based practices for their patients. Although CME for HCPs has traditionally been delivered using face-to-face formats, web-based educational activities now offer a viable alternative approach [33]. To date, several studies have demonstrated the effectiveness of web-based HCP education for breast cancer [34-36]. However, gaps remain in the provision of independent web-based medical education programs for high-risk EBC treatment and effective SDM. Although a small number of programs have been developed in EBC [37-39], these have typically been nonaccredited, therefore not providing HCPs with continuing professional development credits for attendance; pharmaceutical company–led, therefore with the potential to be perceived as promotional; and restricted or limited in terms of access; therefore only accessible to those with the means to do so. To address these gaps and complement the currently available programs, accredited, independent, expert-led education available on free-to-access platforms is required to support the knowledge, competence, and performance of HCPs.

Study Rationale, Objectives, and Aims

An expanded 7-level framework for assessing the outcomes of CME programs was developed by Moore et al [40] in 2009. This framework evaluates participation (level 1), satisfaction (level 2), knowledge (level 3), competence (level 4), performance (level 5), patient health status (level 6), and community health status (level 7). These levels are now widely used and included in many consensus documents and practice recommendations [41]. To date, published Moore’s level 5 [40] outcomes analyses in medical education have largely used subjective self-reported outcomes [42-44]. Although these can provide valuable insights, they can be open to bias, for example, recall bias or social desirability bias [45,46]. An analysis of anonymized patient records provides a complementary objective measure of performance that may enhance the understanding of physician behavior changes in practice.

In this study, we developed and implemented 2 faculty-led, CME-accredited web-based educational activities in high-risk EBC. The objectives of this study were to (1) measure changes in knowledge, competence, and self-reported performance after participation in the activities; (2) objectively evaluate changes in performance using anonymized patient records; and (3) identify the remaining educational gaps.


Study Design

This was a web-based study that analyzed the impact of 2 educational activities in high-risk EBC through HCP questionnaires and deidentified patient records. The target audience comprised oncologists (including breast cancer surgeons), oncology nurse specialists, pathologists, and radiologists from Asia, Brazil, and Europe (excluding the United Kingdom). Satisfaction, knowledge, competence, and performance were assessed according to levels 2 to 5 of the expanded framework for assessing the outcomes of CME programs by Moore et al [40] using self-reported questionnaires and anonymized data extracted from patient records. Questionnaire distribution and data collection were carried out by an independent third party (nuaxia Limited, United Kingdom).

Ethical Considerations

All consents and ethical confirmations for this study were obtained before the completion of both outcome questionnaires. The personal data of HCPs and patients were anonymized. General Data Protection Regulation [47] consents were obtained in the European Union and North America for each questionnaire; adherence to additional requirements in local markets was required to be confirmed in line with European Pharmaceutical Market Research Association professional guidance [48]. For respondents to the patient records questionnaire, consents and ethical confirmations were obtained as part of the questionnaire in accordance with the British Healthcare Business Intelligence Association professional guidelines [49] to ensure patient confidentiality. As part of their written consent to participate in the questionnaires, the HCPs were required to agree to the statement, “As with all research, your identity and personal data are strictly confidential and will not be revealed without your explicit further consent. You have the right to withdraw your consent to participate in market research at any time.” Complete patient records were not obtained by touch Independent Medical Education (touchIME) or any third party; the HCPs were instructed to extract the required anonymized information into a questionnaire. Ethics approval was not applicable for this study because this analysis was not classified as “health research” according to the UK Research and Innovation definition that guides whether research requires Research Ethics Committee review and Health Research Authority approval [50,51]. The study was defined as “market research” per rule 1.1 of the European Pharmaceutical Market Research Association code of conduct, which states that market research does not require a Clinical Research Ethics Committee or independent review board approval [48].

Educational Activities

Educational gaps and learning objectives were identified before the start of activity development in October 2021 by touchIME (a provider of IME for the global HCP community) through a review of the published literature. The expert faculty members further inputted into the educational gaps and learning objectives at the start of activity development. Expert faculty members with a background in breast cancer and SDM were identified by touchIME medical directors through searches of literature indexed in the PubMed database, congress websites, and web-based educational videos. Patient faculty were identified using social media searches across multiple channels. The faculty members (CB, FB, MG, NH, CSH and KLA) were blinded to the plans to assess participation and satisfaction with the education and to publish the outcomes. All the expert faculty (CB, FB, MG, NH, CSH and KLA) involved in the educational activities are authors of this manuscript.

A total of 2 web-based educational activities, touchMDT: “how can shared decision-making be successfully integrated to optimize care of patients with high-risk early breast cancer?” and touchPANEL DISCUSSION: “new horizons in high-risk HR+ HER2- EBC: Risk stratification for early identification and novel treatment strategies” were developed by touchIME in collaboration with the faculty members (CB, FB, MG, NH, CSH and KLA; complete details and learning objectives are included in Multimedia Appendix 1). The touchMDT activity comprised three 13- to 15-minute videos, providing 42 minutes of education in total, and the touchPANEL DISCUSSION activity comprised three 11- to 15-minute videos, providing 39 minutes of education in total. The activities were CME accredited by the Accreditation Council for Continuing Medical Education and the American Nurses Credentialing Center at the University of South Florida Health. Both activities were translated (video subtitles and downloadable slides) from English into Brazilian Portuguese, Chinese Mandarin, French, German, Italian, and Spanish by an independent third party (UnBabel, United States), and both activities were free to access for 1 year (the permissible lifetime of an accredited educational activity) on the touchONCOLOGY website from March 30, 2022, to March 30, 2023 (touchMDT) and from June 15, 2022, to June 15, 2023 (touchPANEL DISCUSSION). The 2 activities featured together on the host website, but participation in both activities was not mandatory.

Various communication channels were used to reach the target audience, including direct publicity emails to the touchONCOLOGY database within the first 12 weeks of the activity launch, with a further reminder at around 6 months; display banners on the touchONCOLOGY website; advertisements in the peer-reviewed journal touchREVIEWS in Oncology and Haematology; publicity via various relevant medical society partnerships; and social media partnerships on Facebook (Meta Platforms, Inc), LinkedIn (Microsoft Corp), and Twitter (rebranded as X; X Corp) targeted at the HCPs throughout the lifetime of the activity.

Assessment of Educational Outcomes

Levels 1 and 2 (Participation and Satisfaction)

Levels 1 (participation) and 2 (satisfaction) were assessed separately for each activity (Multimedia Appendix 2). Level 1 included the number of HCPs who engaged in the web-based educational activities and the average time they spent viewing the videos, and it was the only assessment not evaluated using a questionnaire.

Level 2 (satisfaction) was assessed by scoring 5 statements of satisfaction (using a Likert scale) in a postactivity questionnaire.

Levels 3 to 4 and Level 5 (Knowledge, Competence, and Performance)

Levels 3 to 4 and level 5 were assessed using questionnaires completed by relevant respondents (HCPs completing the questionnaire before the activity) and learners (HCPs completing the questionnaire following the education). No pretesting was performed. The target audience was predefined by specialty (eg, oncologists [including breast cancer surgeons], oncology nurse specialists, pathologists, and radiologists) and by region (Brazil, France, Germany, Italy, and Spain). To avoid any pre-exposure bias and to obtain a statistically representative sample size, data were collected using an independent samples model for each activity. For levels 3 to 4, separate questionnaires were developed for each activity (each comprising 7 questions), whereas for level 5, a combined questionnaire was developed for both activities (3 questions each for touchMDT and touchPANEL DISCUSSION). All questions were developed by touchIME medical directors and writers and were approved for medical accuracy by the faculty. An overview of the topics and the complete questionnaires are provided in Multimedia Appendices 3 to 6.

For the touchPANEL DISCUSSION activity, changes in performance were also assessed through an evaluation of redacted patient records. The HCPs were sent a web-based questionnaire that captured data on (1) general patient demographics and history, (2) risk assessment and stratification to predict disease recurrence, and (3) treatment. Each HCP was requested to extract all relevant nonidentifiable information from a single anonymized patient record into the questionnaire.

Self-Reported Confidence and Intention to Change Practice

As part of the questionnaires, respondents and learners were asked, “How confident are you in treating patients with breast cancer?” (mutually exclusive responses: “not confident,” “a little confident,” “somewhat confident,” “moderately confident,” and “extremely confident”) and “As a result of your participation in this session, will you make a change in your practice?” (mutually exclusive responses: “yes,” “uncertain—more education needed,” “uncertain—practical limitations,” “no—more education needed,” and “no—practical limitations”).

Identification of Outstanding Educational Gaps

A total of 5 potential educational gaps were included in the levels 3 to 4 and level 5 questionnaires (Multimedia Appendix 7), and the learners were asked to rank them by importance. The results were analyzed using a single transferable vote system (Multimedia Appendix 8 [52]). In addition, questions that were answered incorrectly by ≥30% (15/50) of the learners in all postactivity questionnaires were identified as educational gaps. The 30% cutoff was determined by touchIME as an indicator of the requirement for further education based on analyses of data from previous outcomes.

Fielding of the Questionnaires

Preactivity levels 3 to 4 questionnaires were fielded 1 to 2 weeks before launch, whereas postactivity levels 2 to 4 questionnaires were fielded immediately after launch to a different set of HCPs who had participated in the education. The questionnaires were distributed to a database of 20,420 HCPs and then “closed” once a prespecified number had responded (n=50).

The level 5 questionnaire and first patient records questionnaire were fielded 1 to 2 weeks before launch—to a different set of HCPs than those who answered the levels 3 to 4 questionnaires—and closed after completion by a prespecified number of respondents (n=50). A total of 26 weeks after launch, the postactivity level 5 questionnaire and second patient records questionnaire were distributed to the same set of HCPs who completed the level 5 questionnaire and patient records questionnaire before launch. Because of drop out over time, additional HCPs who were matched to the dropouts were surveyed postactivity, if needed.

The HCP participants’ specialties were all validated by nuaxia Limited against third-party data with the assistance of artificial intelligence. This comprised any combination of data from professional associations, hospitals, professional publications, and prescribing and insurance databases.

The participants were required to answer “yes” to the screening question “Do you treat patients with early breast cancer?” to be eligible to participate in the questionnaire study. The HCPs eligible to participate received an honorarium in the form of a digital reward, which could be redeemed via a number of reward partners. In accordance with industry regulations and professional body guidance, the honorarium received was limited to the fair market value for an HCP of that seniority.

Statistical Analyses

Data were analyzed using SPSS Statistics software (version 28.0.1; IBM Corp). The sample size (50 respondents and 50 learners for each activity) was predetermined by the level of funding, and by applying a power analysis, we determined a resulting margin of error of 10% for both the touchMDT and touchPANEL DISCUSSION. Knowledge, competence, and self-reported outcomes were compared for the overall population using an independent samples 2-tailed t test. Data were subdivided by region and years of experience, and a 2-way ANOVA was used to assess the variation in results by these demographics. Individual questions were analyzed with a paired samples 2-tailed t test and a 1-way ANOVA, followed by a cluster analysis, to provide insights into the overall change in correct answers across the questions asked and the specific changes in all the answers given. Data on the number of questions answered correctly were measured as a continuous variable. At the individual question level, the answers were categorical. For performance, measured by the redacted patient records questionnaire, pre- and postactivity comparisons were made using paired and independent samples 2-tailed t tests, chi-square tests, and cluster analysis. These tests were used to assess patient history, use of risk assessment and stratification strategies, and patient treatment pathways.


Assessment of Educational Outcomes

Levels 1 and 2 (Participation and Satisfaction)

By 6 months after launch, 7047 and 8989 participants had engaged with the touchMDT and touchPANEL DISCUSSION activities, respectively. The participants were predominantly oncologists, and the majority were based in Italy for the touchMDT and Brazil for the touchPANEL DISCUSSION activities (Multimedia Appendix 9). Overall satisfaction was 82% (a total score of 20.6 out of 25) for touchMDT and 88% (a total score of 21.9 out of 25) for touchPANEL DISCUSSION (Multimedia Appendix 10). Multichannel publicity reach and impact for the touchMDT and touchPANEL DISCUSSION activities are reported in Multimedia Appendix 11.

Levels 3 and 4 (Knowledge and Competence)

A total of 50 respondents and 50 learners were questioned to assess levels 3 to 4 outcomes (Table 1).

Table 1. Demographics of participating health care professionals (HCPs) for the touchMDT and touchPANEL DISCUSSION activitiesa.
Demographics of HCPsLevels 2 to 4 questionnaireLevel 5 questionnaire

touchMDTtouchPANEL DISCUSSIONBoth activities

RespondentsLearnersRespondentsLearnersRespondentsLearners
Participants, N505050505050
Specialty, n (%)

Oncologist40 (80)42 (84)44 (88)47 (94)43 (86)42 (84)

Radiologist0 (0)0 (0)6 (12)3 (6)4 (8)3 (6)

Pathologist0 (0)0 (0)0 (0)0 (0)3 (6)5 (10)

Radiologist and pathologist10 (20)8 (16)0 (0)0 (0)0 (0)0 (0)
Years of practice, n (%)

<1 to 56 (12)5 (10)N/AbN/AN/AN/A

>5 to 2029 (58)25 (50)N/AN/AN/AN/A

<10N/AN/A10 (20)11 (22)N/AN/A

10 to 20N/AN/A27 (54)27 (54)N/AN/A

0 to 20N/AN/AN/AN/A30 (60)32 (64)

>2015 (30)20 (40)13 (26)12 (24)20 (40)18 (36)
Country, n (%)

Brazil14 (28)11 (22)16 (32)15 (30)0 (0)0 (0)

France5 (10)9 (18)5 (10)5 (10)7 (14)7 (14)

Germany14 (28)12 (24)16 (32)10 (20)16 (32)18 (36)

Italy8 (16)9 (18)7 (14)10 (20)13 (26)11 (22)

Spain9 (18)9 (18)6 (12)10 (20)14 (28)14 (28)

aData were collected 6 months after the launch of the touchMDT and touchPANEL DISCUSSION activities on September 29, 2022, and November 21, 2022, respectively. The questionnaire response categories differed between questionnaires and activities, meaning that some options were not applicable. The respondents and learners were the HCPs who completed the pre- and postactivity questionnaires, respectively.

bN/A: not applicable.

For the touchMDT and touchPANEL DISCUSSION activities, respectively, only 12% (6/50) and 18% (9/50) of the respondents answered at least 6 (86%) of the 7 questions correctly before the activity. This increased to 50% (25/50) and 70% (35/50) in the learners, respectively, after the activity (Figure 1). In Figure 1A, the heat maps show the proportion of respondents (N=50) and learners (n=50) who answered a specific number of questions correctly, as displayed by colors ranging from white (the lowest proportion of respondents and learners) to dark red (the highest proportion of respondents and learners). In Figure 1B, the box and whisker plots show the distribution of the number of questions correctly answered by all respondents and learners. In both plots, the horizontal red line within the box indicates the median, the “x” symbol represents the mean, the boxes indicate the IQR, and the vertical lines (whiskers) extend to the range of values, excluding outliers. The outliers are defined as values that fall outside a distance of 1.5 times the IQR from the upper and lower quartiles and are represented by empty circles. The respondents and learners were the HCPs who completed the pre- and postactivity questionnaires, respectively. For both activities, there was a statistically significant increase in the number of correctly answered questions from pre- to postactivity for all participants (touchMDT: median 4.0, IQR 3.0-5.0 to median 5.5, IQR 4.0-7.0; mean 4.00, SD 1.39 to mean 5.30, SD 1.56; P<.001 and touchPANEL DISCUSSION: median 4.0, IQR 4.0-5.0 to median 6.0, IQR 5.0-7.0; mean 4.32, SD 1.30 to mean 5.88, SD 1.49; P<.001; Figure 1). In subgroup analyses, significant increases in the number of correctly answered questions were observed irrespective of specialty or country for both activities and irrespective of years of experience for the touchPANEL DISCUSSION (Multimedia Appendices 12 and 13). Refer to Multimedia Appendix 14 for the responses to individual topics for the levels 3 to 4 questionnaires.

Figure 1. Summary of the number of correct responses for the levels 3 and 4 outcomes questionnaire before and after the launch of touchMDT and touchPANEL DISCUSSION. (A) Heat maps show the proportion of respondents (n=50) and learners (n=50) who answered a specific number of questions correctly, as displayed by colors ranging from white (the lowest proportion of respondents and learners) to dark red (the highest proportion of respondents and learners). (B) Box and whisker plots show the distribution of the number of questions correctly answered by all respondents and learners. In both plots, the horizontal red line within the box indicates the median, the “x” symbol represents the mean, the boxes indicate the IQR, and the vertical lines (whiskers) extend to the range of values, excluding outliers.
Level 5 (Performance)

A total of 50 respondents and 50 learners completed the level 5 questionnaire and the patient records questionnaire (Table 1). The dropout rate was 16% (8/50); therefore, 8 of the 50 learners were de novo HCPs who were matched to the dropouts.

Self-Reported

Preactivity, in total, 6% (3/50) of respondents answered at least 5 (83%) out of 6 questions with the best clinical option. This increased to 44% (22/50) of the learners after the activity (Figure 2). In Figure 2A, the heat maps show the proportion of respondents (n=50) and learners (n=50) who answered a specific number of questions correctly, as displayed by colors ranging from white (the lowest proportion of respondents and learners) to dark red (the highest proportion of respondents and learners). In Figure 2B, the box and whisker plots show the distribution of the number of questions correctly answered by all respondents and learners. The horizontal red line within the box indicates the median, the “x” symbol represents the mean, the boxes indicate the IQR, and the vertical lines (whiskers) extend to the range of values, excluding outliers. The outliers are defined as values that fall outside a distance of 1.5 times the IQR from the upper and lower quartiles and are represented by empty circles. The respondents and learners were HCPs who completed the pre- and postactivity questionnaires, respectively. There was a statistically significant increase in the number of correctly answered questions from pre- to postactivity for all participants (median 3.0, IQR 2.0-3.0 to median 4.0, IQR 3.0-5.0; mean 2.82, SD 1.08 to mean 4.16, SD 1.45; P<.001). Refer to Multimedia Appendix 15 for the responses to individual topics for the level 5 questionnaires.

Figure 2. Summary of the number of correct responses for the level 5 outcomes questionnaire before and after the launch of touchMDT and touchPANEL DISCUSSION. (A) Heat maps show the proportion of respondents (n=50) and learners (n=50) who answered a specific number of questions correctly, as displayed by colors ranging from white (the lowest proportion of respondents and learners) to dark red (the highest proportion of respondents and learners). (B) Box and whisker plots show the distribution of the number of questions correctly answered by all respondents and learners. The horizontal red line within the box indicates the median, the “x” symbol represents the mean, the boxes indicate the IQR, and the vertical lines (whiskers) extend to the range of values, excluding outliers.

In subgroup analyses of data by specialty, years of experience and country (Multimedia Appendix 16), increases in the number of questions with the correct clinical response were observed irrespective of specialty or years of experience, and in the subgroups of participants from Germany, Spain, and Italy.

Patient Record Data

The patient characteristics reported by the respondents and learners were broadly similar (Multimedia Appendix 17). The respondents and learners used a wide range of measures to determine the patient risk of recurrence (30 and 26 different combinations of measures, respectively; Multimedia Appendix 18). There was a significant difference between the number of respondents and learners selecting each measure (χ249=508.474; P<.001) and the number of measures selected (χ256=203.125; P<.001; Multimedia Appendix 19). The Ki-67 index use was >90% for both groups, and most of those who used the Ki-67 index reported patients who had tumors with a Ki-67 score of ≥20% (respondents: 30/48, 62.5% and learners: 30/47, 64%; Figure S1 in Multimedia Appendix 20). There was no significant difference between responders and learners regarding adjuvant therapy when analyzing patient record data by Ki-67 index, menopausal status, germline BRCA status, or the number of positive lymph nodes (Figure S2 in Multimedia Appendix 20).

Self-Reported Confidence and Intention to Change Practice

Results from the levels 3 to 4 and level 5 questionnaires indicated modest increases in confidence in treating patients with EBC from pre- to postactivity, with the proportion of participants reporting that they felt moderately or extremely confident increasing from 72% (36/50) to 78% (39/50; P=.82) for touchMDT and 74% (37/50) to 86% (43/50; P=.49) for touchPANEL DISCUSSION and from 72% (36/50) to 80% (40/50; P=.90) for the level 5 questionnaire (Figure S3 in Multimedia Appendix 20).

At least half of all learners stated that they would make a change to their practice following their participation in the activities (levels 3 to 4 questionnaire: touchMDT—25/50, 50% and touchPANEL DISCUSSION—29/50, 58%; level 5 questionnaire: 26/50, 52%). The reasons given for not making a change were split between the need for more education (levels 3 to 4 questionnaire: touchMDT—12/50, 24% and touchPANEL DISCUSSION—7/50, 14%; level 5 questionnaire: 13/50, 26%) and practical limitations (levels 3 to 4 questionnaire: touchMDT—13/50, 26% and touchPANEL DISCUSSION—14/50, 28%; level 5 questionnaire: 11/50, 22%).

Identification of Outstanding Educational Gaps

In ranking the unmet educational needs, touchMDT learners highlighted “strategies for implementing SDM in clinical practice” and “effective communication strategies in SDM to optimize patient outcomes” as key areas for future education, and touchPANEL DISCUSSION learners highlighted “using genetic and biomarker testing to guide therapy choice” and “individualization of treatment choice in high-risk hormone receptor–positive human epidermal growth factor receptor 2 negative (HR+ HER2–) EBC.” From the level 5 questionnaire, learners highlighted “using genetic and biomarker testing to guide therapy choice for patients with high-risk HR+ HER2- EBC” and “understanding the latest data on emerging treatments for high-risk HR+ HER2- EBC” as their most important unmet educational needs (Table S1 in Multimedia Appendix 20).

For the touchPANEL DISCUSSION, high levels of knowledge and competence were achieved for all 3 learning objectives. However, some unmet needs remained after participation in touchMDT, with 60% (30/50) and 36% (18/50) of the learners, respectively, being unable to demonstrate declarative knowledge of the current consensus on the use of patient decision aids to support SDM in breast cancer and being unable to demonstrate competence in supporting patients in understanding data and reaching a shared decision regarding neoadjuvant systemic therapy. In the level 5 questionnaire, ≥36% (18/50) of the learners were unable to provide the best clinical responses to the questions on reducing the patient burden (18/50, 36%), risk of recurrence (20/50, 40%), and chemotherapy treatment decisions (26/50, 52%).


Principal Findings

This study evaluated the impact of 2 faculty-led, CME-accredited web-based learning activities on EBC. Participation in both activities resulted in high satisfaction scores and statistically significant improvements in self-reported knowledge, competence, and performance. Subgroup analyses indicated that the education was broadly beneficial, regardless of region, specialty, and experience. Patient record data analysis showed statistically significant differences in how the risk of recurrence was determined by responders and learners. The impact of the activities on therapeutic choice was limited, although this may be because of factors such as local guidelines, access to treatments, and individual patient characteristics. Approximately half of the learners (80/150, 53%) stated that they would change their practice in response to the educational material, further suggesting that the activities were valuable learning tools.

Participation in these web-based activities was considerably higher than could be achieved with traditional face-to-face programs and may also reflect the involvement of a multinational panel of recognized experts and the availability of translations. The latter is a major difference from traditional conference-based activities, as they are usually only available in 1 language, typically English.

Although many learners stated that they would change their practice, there remained a considerable number who were uncertain or who would not change their practice at the current time. The reasons for not changing practice were largely split between the requirement for more education and practical limitations. Although learners were not canvassed for specific details regarding practical limitations, we can speculate that they may relate to regional or national differences in institutional resources and structure or regulatory and reimbursement approvals of treatment. Indeed, documented barriers to change in clinical practice include institution-related issues such as flawed leadership and communication and insufficient organizational culture shift, and practical restrictions such as recently updated guidelines and access to emerging drugs [53]. In addition, a 2022 study on factors that influenced HCPs’ intent to put newly acquired learning into practice suggested that a lack of belief in one’s capabilities and the potential consequences of adopting new clinical behaviors can prevent HCPs from translating education into practice [54].

These data demonstrate the potential value of succinct web-based learning activities that are specifically designed to address knowledge gaps in complex and rapidly evolving medical fields. Although published data on outcomes following educational activities with similar methodologies remain limited, the results of this study are consistent with the results of a small number of previous studies in other disease areas [55-57]. Notably, the field of breast cancer is evolving rapidly, and it is essential for oncologists, particularly nonspecialists, to remain informed of the latest findings and recommendations [19-26]. Therefore, focused web-based learning activities may also be valuable for general oncologists to enable them to keep up-to-date with changes in specialist fields.

Strengths and Limitations

There were several strengths associated with this study:

  1. The activities provided a holistic curriculum and unbiased education focused on clearly defined learning objectives.
  2. The activities were translated into several languages and were available on a free-to-access website, which likely increased their global accessibility.
  3. A broad target audience was successfully reached, highlighting the importance of the multichannel publicity strategy and the inclusion of faculty from often underrepresented geographies (Latin America and Asia-Pacific).
  4. The multidisciplinary team approach and inclusion of a survivor of breast cancer ensured that the activities were directly applicable to the participants’ daily practice; the emotive element can also aid learning and retention [58].
  5. The format used in the touchPANEL DISCUSSION allowed the latest evidence to be put into context for practicing physicians.
  6. The development of the education in a short time frame allowed for emerging data to be communicated to the HCPs potentially ahead of publications and conventional educational formats.
  7. A major strength was using an objective measure of performance to complement the more subjective self-reported data.

This study also has several limitations:

  1. The conclusions that could be drawn from the main and subgroup analyses were speculative and limited because of the relatively small sample size.
  2. All medical educational studies are affected by inevitable self-selection bias; that is, the HCPs who feel they lack knowledge on a specific topic are more likely to participate and, therefore, show a bigger impact of the education than might be the case for a wider audience.
  3. This study only evaluated outcomes following 2 specific CME activities in EBC, and the conclusions may not be generalizable to other web-based learning formats.
  4. An independent samples method was used for the levels 3 to 4 questionnaires and the self-reported level 5 questionnaire to avoid pre-exposure bias; however, this meant that the direct impact of education on each learner could not be determined. Therefore, we cannot rule out the possibility that other sources of education may have contributed to the reported outcomes.

Despite these limitations, this study offers the first comprehensive assessment of such activities using an accepted methodology.

Identification of Needs for Further Education in High-Risk EBC

Notably, only 30% (15/50) and 48% (24/50) of the touchMDT and touchPANEL DISCUSSION learners, respectively, answered all questions correctly in the levels 3 to 4 questionnaires. Similarly, only 20% (10/50) of the learners gave the best clinical response for all questions in the level 5 questionnaire. This may, in part, reflect a mixed audience but suggests that further education may be warranted to reinforce the content of these activities. To refine future educational activities, we identified several unmet needs during this study from the questions that were incorrectly answered after the activities. In addition, several self-reported educational gaps were identified, including implementing SDM in clinical practice, using genetic and biomarker testing to guide therapy choices, and understanding the latest data on emerging treatments.

Future Directions

Limitations of traditional CME approaches in affecting changes in physician performance have been previously reported [59]; however, the optimal format for continuing educational activities in both breast cancer and the wider medical field remains to be fully defined. This study and other similar studies show evidence that more engaging approaches have the potential to improve the effectiveness of CME [55-57,60,61]. Evaluation of the long-term impacts of CME on HCP performance, alongside assessment against Moore’s Levels 6 and 7 [40] to determine the effect of education on patient (level 6) and community (level 7) health will add further value to CME programs in the future. Activity formats that may be particularly relevant include experts sharing insights drawn from experience and their own clinical practice, conversational and panel discussion formats, and expert interviews supplemented by vignettes of consultation strategies. Furthermore, web-based delivery may offer scope for developing more individualized approaches. Web-based activities can also be made available as enduring materials, providing a resource designed for optimal HCP accessibility. Future studies will need to be designed to evaluate the comparative effectiveness of these different approaches to CME. In addition, in future studies, a larger sample size will increase the statistical power of the analyses.

Conclusions

Our study demonstrated that focused, free-to-access web-based CME activities on EBC were associated with improvements in HCP knowledge, competence, and self-reported performance. This study addressed the gaps in the provision of HCP-focused web-based IME programs that encompass recent advances in the high-risk EBC treatment landscape, the need for and approaches to effective SDM, and the gaps within the literature in terms of reporting outcomes from web-based CME activities. The identified unmet needs should be used to inform the design of future educational activities for this disease area. Further studies evaluating the long-term impact of education on HCP performance and on patient and community health will be valuable in defining the clinical impact of CME and the most effective channels for its delivery.

Acknowledgments

Medical writing support was provided by Steph Carter, and editorial support was provided by Cheryl Brant, both from touch Independent Medical Education (touchIME), Cheshire, United Kingdom. The educational activities were jointly provided by the University of South Florida Health and touchIME. The authors would like to thank the touchIME audience outreach team (Joel Turner, Hannah Morton-Fishwick, and Louise Jarman) for the collection and analysis of the level 1 data. The authors would like to thank former employee of touchIME Sonia Mills for additional editorial support. Eli Lilly provided an independent medical education grant to fund the educational activity, medical writing, and editorial support but did not contribute directly to manuscript development, the decision to submit, or the submission process.

Data Availability

The data sets generated during and/or analyzed during this study are available from the corresponding author on reasonable request.

Authors' Contributions

All authors contributed to the conceptualization, formal analysis of the data, and writing (review and editing) of the manuscript.

KB, SN, A Noble, A Nunn and CS contributed to the investigation, methodology, project administration, visualization of the study, and writing (original draft) of the manuscript. SN contributed to the funding acquisition for and supervision of the manuscript. A Noble contributed to data curation.

Conflicts of Interest

CB reports receiving advisory board fees from AstraZeneca, Bayer, Boehringer Ingelheim, Eisai, GlaxoSmithKline, Lilly, MSD, Novartis, Pfizer, Genentech (Roche), Sanofi, and Zodiac Pharma; consultancy fees from AstraZeneca, Bayer, Boehringer Ingelheim, Eisai, GlaxoSmithKline, Lilly, MSD, Novartis, Pfizer, Genentech (Roche), Sanofi, and Zodiac Pharma; grants and research support from AbbVie, Abraxis Biosciences, AB Science, Amgen, Asana Biosciences, Astellas Pharma, AstraZeneca, BioMarin, Boehringer Ingelheim, Bristol Myers Squibb, Daiichi Sankyo, Exelixis, GlaxoSmithKline, ImClone Systems, LEO Pharma, Lilly, Medivation, MSD, Merck KGaA, Merrimack, Millennium, Mylan, Novartis, Pfizer, PharmaMar, Polyphor, Genentech (Roche), Sanofi, Shanghai Henlius Biotech, and Taiho Pharmaceutical; and holding stock and shares (self-managed) in MEDSIR and Tummi. FB reports receiving advisory board fees from Eisai, Eli Lilly, Gilead, MSD, Novartis, Pfizer, and Roche and consultancy fees from Eli Lilly. MG reports receiving personal fees and travel support from AstraZeneca, Daiichi Sankyo, Eli Lilly, Menarini-Stemline, MSD, Novartis, Pierre Fabre, and Veracyte, and his immediate family member is employed by Sandoz. NH reports receiving consultancy fees from Gilead, Roche, Sandoz, and Seagen and speaker bureau fees from AstraZeneca, Daiichi Sankyo, Gilead, Lilly, MSD, Novartis, Pierre Fabre, Pfizer, Roche, and Seagen. CSH reports receiving advisory board fees from AstraZeneca, Lilly, Pfizer, Novartis, and Roche; grants and research support from AstraZeneca, Daiichi Sankyo, EirGenix, Lilly, MSD, Novartis, OBI Pharma, Pfizer, and Roche; and speaker bureau fees from AstraZeneca, Novartis, Pfizer, and Roche. KLA has no interests or relationships or affiliations to disclose. KB, SN, A Noble, A Nunn and CS are employees of touch Independent Medical Education Limited.

Multimedia Appendix 1

Activity development process.

DOCX File , 25 KB

Multimedia Appendix 2

Assessment of participation (level 1) and satisfaction (level 2).

DOCX File , 22 KB

Multimedia Appendix 3

Topics included in levels 3 and 4 and level 5 outcomes questionnaires.

DOCX File , 13 KB

Multimedia Appendix 4

Questions included in the levels 3 and 4 outcomes questionnaire for the touchMDT activity.

DOCX File , 16 KB

Multimedia Appendix 5

Questions included in the levels 3 and 4 outcomes questionnaire for the touchPANEL DISCUSSION activity.

DOCX File , 16 KB

Multimedia Appendix 6

Questions included in the level 5 outcomes questionnaire for the touchMDT and touchPANEL DISCUSSION activities.

DOCX File , 16 KB

Multimedia Appendix 7

Unmet educational need options included in levels 3 to 4 and level 5 questionnaires.

DOCX File , 13 KB

Multimedia Appendix 8

Single transferable vote system methodology.

DOCX File , 12 KB

Multimedia Appendix 9

Engagement results and demographics for the touchMDT and touchPANEL DISCUSSION activities.

DOCX File , 14 KB

Multimedia Appendix 10

Mean satisfaction scores of levels 2 to 4 questionnaire (out of a maximum of 5) completed by touchMDT and touchPANEL DISCUSSION learners.

DOCX File , 13 KB

Multimedia Appendix 11

Multichannel publicity reach and impact for the touchMDT and touchPANEL DISCUSSION activities.

DOCX File , 13 KB

Multimedia Appendix 12

Mean number of correct responses for the levels 3 and 4 outcomes questionnaire before and after the launch of touchMDT by (A) country, (B) years of experience, and (C) specialty subgroups of the respondents and learners.

DOCX File , 71 KB

Multimedia Appendix 13

Mean number of correct responses for the levels 3 and 4 outcomes questionnaire before and after the launch of touchPANEL DISCUSSION by (A) country, (B) level of experience, and (C) specialty of the respondents and learners.

DOCX File , 68 KB

Multimedia Appendix 14

Summary of correct responses for individual topics for the levels 3 and 4 outcomes questionnaire before and after the launch of (A) touchMDT and (B) touchPANEL DISCUSSION.

DOCX File , 60 KB

Multimedia Appendix 15

Summary of correct responses for individual topics for the level 5 outcomes questionnaire before and after the launch of touchMDT and touchPANEL DISCUSSION.

DOCX File , 31 KB

Multimedia Appendix 16

Mean number of correct responses for the level 5 outcomes questionnaire before and after the launch of touchMDT and touchPANEL DISCUSSION by (A) country, (B) level of experience, and (C) specialty of the respondents and learners.

DOCX File , 102 KB

Multimedia Appendix 17

Patient characteristics from patient records data (level 5) submitted by responders and learners for the touchPANEL DISCUSSION activity.

DOCX File , 15 KB

Multimedia Appendix 18

Combinations of measures used to determine patient risk for recurrence from patient records data (level 5) submitted by responders and learners for the touchPANEL DISCUSSION activity.

DOCX File , 15 KB

Multimedia Appendix 19

Measures used to determine patient risk for recurrence reported by respondents and learners in the level 5 patient records questionnaire.

DOCX File , 42 KB

Multimedia Appendix 20

Ki-67 use and Ki-67 index scores reported by respondents and learners in the level 5 patient records questionnaire (Figure S1); adjuvant or planned adjuvant therapy reported by respondents and learners in the level 5 patient records questionnaire (Figure S2); changes in self-reported confidence in (A) levels 3 to 4 questionnaires and (B) level 5 questionnaires following participation in the touchMDT and touchPANEL DISCUSSION activities (Figure S3); unmet educational needs identified by the touchMDT and touchPANEL DISCUSSION learners (Table S1).

DOCX File , 423 KB

  1. Katz SJ, Belkora J, Elwyn G. Shared decision making for treatment of cancer: challenges and opportunities. J Oncol Pract. May 2014;10(3):206-208. [FREE Full text] [CrossRef] [Medline]
  2. Gustafson A. Reducing patient uncertainty: implementation of a shared decision-making process enhances treatment quality and provider communication. Clin J Oncol Nurs. Feb 01, 2017;21(1):113-115. [CrossRef] [Medline]
  3. NQP shared decision making action brief. National Quality Forum. Oct 2017. URL: https://www.qualityforum.org/Publications/2017/10/NQP_Shared_Decision_Making_Action_Brief.aspx [accessed 2024-01-11]
  4. Barrios C, Sánchez-Vanegas G, Villarreal-Garza C, Ossa A, Lombana MA, Monterrosa-Blanco A, et al. Barriers and facilitators to provide multidisciplinary care for breast cancer patients in five Latin American countries: a descriptive-interpretative qualitative study. Lancet Reg Health Am. Jul 2022;11:100254. [FREE Full text] [CrossRef] [Medline]
  5. Cardoso F, Kyriakides S, Ohno S, Penault-Llorca F, Poortmans P, Rubio IT, et al. Early breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. Oct 01, 2019;30(10):1674. [FREE Full text] [CrossRef] [Medline]
  6. Cardoso F, MacNeill F, Penault-Llorca F, Eniu A, Sardanelli F, Nordström EB, et al. Why is appropriate healthcare inaccessible for many European breast cancer patients? - The EBCC 12 manifesto. Breast. Feb 2021;55:128-135. [FREE Full text] [CrossRef] [Medline]
  7. National Comprehensive Cancer Network home page. National Comprehensive Cancer Network. URL: https://www.nccn.org/ [accessed 2024-01-11]
  8. Spronk I, Burgers JS, Schellevis FG, van Vliet LM, Korevaar JC. The availability and effectiveness of tools supporting shared decision making in metastatic breast cancer care: a review. BMC Palliat Care. May 11, 2018;17(1):74. [FREE Full text] [CrossRef] [Medline]
  9. Stacey D, Légaré F, Lewis K, Barry MJ, Bennett CL, Eden KB, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. Apr 12, 2017;4(4):CD001431. [FREE Full text] [CrossRef] [Medline]
  10. Ankolekar A, Dekker A, Fijten R, Berlanga A. The benefits and challenges of using patient decision aids to support shared decision making in health care. JCO Clin Cancer Inform. Dec 2018;2:1-10. [FREE Full text] [CrossRef] [Medline]
  11. Savelberg W, Boersma LJ, Smidt M, Goossens MF, Hermanns R, van der Weijden T. Does lack of deeper understanding of shared decision making explains the suboptimal performance on crucial parts of it? An example from breast cancer care. Eur J Oncol Nurs. Feb 2019;38:92-97. [FREE Full text] [CrossRef] [Medline]
  12. Covvey JR, Kamal KM, Gorse EE, Mehta Z, Dhumal T, Heidari E, et al. Barriers and facilitators to shared decision-making in oncology: a systematic review of the literature. Support Care Cancer. May 2019;27(5):1613-1637. [CrossRef] [Medline]
  13. Pourgholam N, Shoghi M, Borimnejad L. Patients' lived experiences of the paternalistic care behavior: a qualitative study. J Caring Sci. Aug 2022;11(3):163-171. [FREE Full text] [CrossRef] [Medline]
  14. Thompson GA, Segura J, Cruz D, Arnita C, Whiffen LH. Cultural differences in patients' preferences for paternalism: comparing Mexican and American patients' preferences for and experiences with physician paternalism and patient autonomy. Int J Environ Res Public Health. Aug 26, 2022;19(17):10663. [FREE Full text] [CrossRef] [Medline]
  15. Gil-Gil M, Alba E, Gavilá J, de la Haba-Rodríguez J, Ciruelos E, Tolosa P, et al. The role of CDK4/6 inhibitors in early breast cancer. Breast. Aug 2021;58:160-169. [FREE Full text] [CrossRef] [Medline]
  16. Harbeck N, Rastogi P, Martin M, Tolaney SM, Shao ZM, Fasching PA, et al. Adjuvant abemaciclib combined with endocrine therapy for high-risk early breast cancer: updated efficacy and Ki-67 analysis from the monarchE study. Ann Oncol. Dec 2021;32(12):1571-1581. [FREE Full text] [CrossRef] [Medline]
  17. Gnant M, Dueck AC, Frantal S, Martin M, Burstein HJ, Greil R, et al. Adjuvant palbociclib for early breast cancer: the PALLAS trial results (ABCSG-42/AFT-05/BIG-14-03). J Clin Oncol. Jan 20, 2022;40(3):282-293. [FREE Full text] [CrossRef] [Medline]
  18. Loibl S, Marmé F, Martin M, Untch M, Bonnefoi H, Kim SB, et al. Palbociclib for residual high-risk invasive HR-positive and HER2-negative early breast cancer-the Penelope-B trial. J Clin Oncol. May 10, 2021;39(14):1518-1530. [CrossRef] [Medline]
  19. Harbeck N. Risk-adapted adjuvant therapy of luminal early breast cancer in 2020. Curr Opin Obstet Gynecol. Feb 01, 2021;33(1):53-58. [CrossRef] [Medline]
  20. Turner N, Howell S, Jhaveri K, Gomez H, Toi M, Hu X, et al. 350TiP A phase III trial of capivasertib and fulvestrant versus placebo and fulvestrant in patients with HR+/HER2− breast cancer (CAPItello-291). Ann Oncol. Sep 2020;31:S388-S389. [CrossRef]
  21. Ditsch N, Wöcke A, Untch M, Jackisch C, Albert US, Banys-Paluchowski M, et al. AGO recommendations for the diagnosis and treatment of patients with early breast cancer: update 2022. Breast Care (Basel). Aug 2022;17(4):403-420. [FREE Full text] [CrossRef] [Medline]
  22. Burstein HJ, Curigliano G, Thürlimann B, Weber WP, Poortmans P, Regan MM, et al. Customizing local and systemic therapies for women with early breast cancer: the St. Gallen International Consensus Guidelines for treatment of early breast cancer 2021. Ann Oncol. Oct 2021;32(10):1216-1235. [FREE Full text] [CrossRef] [Medline]
  23. Moy B, Rumble RB, Carey LA, Chemotherapy and Targeted Therapy for Endocrine-Pretreated or Hormone Receptor–Negative Metastatic Breast Cancer Expert Panel. Chemotherapy and targeted therapy for endocrine-pretreated or hormone receptor-negative metastatic breast cancer: ASCO guideline rapid recommendation update. J Clin Oncol. Feb 20, 2023;41(6):1318-1320. [CrossRef] [Medline]
  24. Gradishar WJ, Moran MS, Abraham J, Aft R, Agnese D, Allison KH, et al. Breast cancer, version 3.2022, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. Jun 2022;20(6):691-722. [CrossRef] [Medline]
  25. Gnant M, Fitzal F, Rinnerthaler G, Steger GG, Greil-Ressler S, Balic M, et al. Duration of adjuvant aromatase-inhibitor therapy in postmenopausal breast cancer. N Engl J Med. Jul 29, 2021;385(5):395-405. [CrossRef] [Medline]
  26. Gnant M, Frantal M, Pfeiler G, Steger GG, Egle D, Greil R, et al. Long-term outcomes of adjuvant denosumab in breast cancer. NEJM Evidence. Nov 22, 2022;1(12). [FREE Full text] [CrossRef]
  27. Harbeck N, Gnant M. Breast cancer. Lancet. Mar 18, 2017;389(10074):1134-1150. [CrossRef] [Medline]
  28. Thomssen C, Balic M, Harbeck N, Gnant M. St. Gallen/Vienna 2021: a brief summary of the consensus discussion on customizing therapies for women with early breast cancer. Breast Care (Basel). Apr 2021;16(2):135-143. [FREE Full text] [CrossRef] [Medline]
  29. Kristensen N, Nymann C, Konradsen H. Implementing research results in clinical practice- the experiences of healthcare professionals. BMC Health Serv Res. Feb 10, 2016;16(1):48. [FREE Full text] [CrossRef] [Medline]
  30. Beatty PA. Coping with abundance: the burden of progress in medical oncology. Oncologist. 2012;17(2):294-295. [FREE Full text] [CrossRef] [Medline]
  31. Charlton M, Schlichting J, Chioreso C, Ward M, Vikas P. Challenges of rural cancer care in the United States. Oncology (Williston Park). Sep 2015;29(9):633-640. [Medline]
  32. Morris ZS, Wooding S, Grant J. The answer is 17 years, what is the question: understanding time lags in translational research. J R Soc Med. Dec 2011;104(12):510-520. [FREE Full text] [CrossRef] [Medline]
  33. Ngenzi JL, Scott RE, Mars M. Information and communication technology to enhance continuing professional development (CPD) and continuing medical education (CME) for Rwanda: a scoping review of reviews. BMC Med Educ. Apr 29, 2021;21(1):245. [FREE Full text] [CrossRef] [Medline]
  34. Meani F, Kovacs T, Wandschneider W, Costa A, Pagani O. Multidisciplinary blended learning to build a breast cancer specialist career: survey on the perspective of the first 2 cohorts of the ESO-ULM Certificate of Competence in Breast cancer (CCB). BMC Med Educ. May 05, 2022;22(1):344. [FREE Full text] [CrossRef] [Medline]
  35. Dorkhom N, Middleton D, Guedj P, Chen P, Lucero K, Curigliano G. An outcomes summary of the clinical advances curriculum on CDK4 and 6 inhibition in breast cancer. Ann Oncol. May 2020;31:S77. [FREE Full text] [CrossRef]
  36. Walling BM, Totzkay D, Silk KJ, Boumis JK, Thomas B, Smith S. Evaluating the feasibility of continuing medical education for disseminating emerging science on the breast cancer and environment connection. J Health Commun. Jun 03, 2021;26(6):391-401. [FREE Full text] [CrossRef] [Medline]
  37. Loibl S, de Azambuja E, Johnston S, Dawood S. Raising the bar for patients with HR+/HER2- early breast cancer. ESMO. May 25, 2022. URL: https://tinyurl.com/2cb3scha [accessed 2024-01-11]
  38. Disease education resources: oncology. Lilly. URL: https://tinyurl.com/mup6jche [accessed 2024-01-11]
  39. Johnston SR. Assessing risk in early HR+/HER2- breast cancer management: a patient clinic. Medscape. May 26, 2021. URL: https://www.medscape.org/viewarticle/951798 [accessed 2024-01-11]
  40. Moore DEJ, Green JS, Gallis HA. Achieving desired results and improved outcomes: integrating planning and assessment throughout learning activities. J Contin Educ Health Prof. 2009;29(1):1-15. [CrossRef] [Medline]
  41. Bannister J, Neve M, Kolanko C. Increased educational reach through a microlearning approach: can higher participation translate to improved outcomes? J Eur CME. Oct 20, 2020;9(1):1834761. [FREE Full text] [CrossRef] [Medline]
  42. Milgrom ZZ, Severance TS, Scanlon CM, Carson AT, Janota AD, Vik TA, et al. An evaluation of an Extension for Community Healthcare Outcomes (ECHO) intervention in cancer prevention and survivorship care. BMC Med Inform Decis Mak. May 17, 2022;22(1):135. [FREE Full text] [CrossRef] [Medline]
  43. Ivanova A, Baliunas D, Ahad S, Tanzini E, Dragonetti R, Fahim M, et al. Performance change in treating tobacco addiction: an online, interprofessional, facilitated continuing education course (TEACH) evaluation at Moore's level 5. J Contin Educ Health Prof. Jan 01, 2021;41(1):31-38. [CrossRef] [Medline]
  44. Bednář J, Buchanan J, Michels NR, Kalda R, Vajer P, Miftode R, et al. Current state of the evidence-base for effective continuous medical education for family medicine and general practice. European Academy of Teachers in General Practice and Family Medicine (EURACT). 2021. URL: https://tinyurl.com/4469rddt [accessed 2024-02-20]
  45. Rosenman R, Tennekoon V, Hill LG. Measuring bias in self-reported data. Int J Behav Healthc Res. Oct 2011;2(4):320-332. [FREE Full text] [CrossRef] [Medline]
  46. Althubaiti A. Information bias in health research: definition, pitfalls, and adjustment methods. J Multidiscip Healthc. 2016;9:211-217. [FREE Full text] [CrossRef] [Medline]
  47. Regulation (EU) 2016/679 of the European parliament and of the council of 27 April 2016. Official Journal of the European Union. May 4, 2016. URL: https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32016R0679 [accessed 2024-01-19]
  48. Code of conduct. European Pharmaceutical Market Research Association. Sep 2023. URL: https://tinyurl.com/242pp57k [accessed 2024-01-26]
  49. Guidelines and legislation. British Healthcare Business Intelligence Association. URL: https://www.bhbia.org.uk/guidelines-and-legislation [accessed 2024-01-26]
  50. Understanding health research. UK Research and Innovation. URL: https://tinyurl.com/4u32dw35 [accessed 2024-01-26]
  51. Research Ethics Committee review. National Health Service Health Research Authority. URL: https://tinyurl.com/mswuu6c6 [accessed 2024-01-26]
  52. Tideman N. The single transferable vote. J Econ Perspect. Feb 01, 1995;9(1):27-38. [CrossRef]
  53. Barach PR. Addressing barriers for change in clinical practice. In: Guidet B, Valentin A, Flaatten H, editors. Quality Management in Intensive Care: A Practical Guide. Cambridge, UK. Cambridge University Press; 2016.
  54. Bergeron L, Décary S, Djade CD, Daniel SJ, Tremblay M, Rivest LP, et al. Factors associated with specialists' intention to adopt new behaviors after taking web-based continuing professional development courses: cross-sectional study. JMIR Med Educ. Jun 02, 2022;8(2):e34299. [FREE Full text] [CrossRef] [Medline]
  55. Harris SB, Idzik S, Boasso A, Neunie SQ, Noble AD, Such HE, et al. The educational impact of web-based, faculty-led continuing medical education programs in type 2 diabetes: a survey study to analyze changes in knowledge, competence, and performance of health care professionals. JMIR Med Educ. Oct 14, 2022;8(4):e40520. [FREE Full text] [CrossRef] [Medline]
  56. Larkin A, Schrand J, Le A. Success of CME at improving knowledge of clinical use of real-time CGM. Diabetes. 2021;70(Supplement_1):614P. [FREE Full text] [CrossRef]
  57. Rohani-Montez C, Gunesekera D, Coppo P. Effectiveness of interactive case-based online education in improving Attp diagnosis and treatment selection. Blood. Nov 2020;136(Supplement 1):36-37. [CrossRef]
  58. Tyng CM, Amin HU, Saad MN, Malik AS. The influences of emotion on learning and memory. Front Psychol. Aug 24, 2017;8:1454. [FREE Full text] [CrossRef] [Medline]
  59. Davis D, O'Brien MA, Freemantle N, Wolf FM, Mazmanian P, Taylor-Vaisey A. Impact of formal continuing medical education: do conferences, workshops, rounds, and other traditional continuing education activities change physician behavior or health care outcomes? JAMA. Sep 01, 1999;282(9):867-874. [CrossRef] [Medline]
  60. Diehl LA, Souza RM, Gordan PA, Esteves RZ, Coelho IC. InsuOnline, an electronic game for medical education on insulin therapy: a randomized controlled trial with primary care physicians. J Med Internet Res. Mar 09, 2017;19(3):e72. [FREE Full text] [CrossRef] [Medline]
  61. Wiecha J, Heyden R, Sternthal E, Merialdi M. Learning in a virtual world: experience with using second life for medical education. J Med Internet Res. Jan 23, 2010;12(1):e1. [FREE Full text] [CrossRef] [Medline]


Akt: protein kinase B
CME: continuing medical education
EBC: early breast cancer
HCP: health care professional
SDM: shared decision-making
touchIME: touch Independent Medical Education


Edited by A Mavragani; submitted 24.07.23; peer-reviewed by J Lapointe, N Than, S Ganesh; comments to author 09.01.24; revised version received 06.02.24; accepted 07.02.24; published 21.03.24.

Copyright

©Michael Gnant, Khatijah Lim Abdullah, Frances Boyle, Chiun-Sheng Huang, Katie Bickford, Sola Neunie, Alexander Noble, Anne Nunn, Caroline Sproat, Nadia Harbeck, Carlos Barrios. Originally published in JMIR Formative Research (https://formative.jmir.org), 21.03.2024.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Formative Research, is properly cited. The complete bibliographic information, a link to the original publication on https://formative.jmir.org, as well as this copyright and license information must be included.