Figure 1 shows the flow of this study. First, the extant literature was reviewed narratively, and an expert panel was selected using purposive and snowball sampling methods. Then, Delphi rounds were held using web technology [20,21,22]. Competencies and EPA items identified by the Delphi rounds were confirmed and discussed through a non-anonymous web conference between the expert panel and three external evaluators. Lastly, another Delphi round was held to finalize the competency and EPA items. The Delphi process was conducted between August 2020 and January 2021 in Japan according to the Guidance on Conducting and REporting DElphi Studies [22].
Design
The current study was conducted using a modified Delphi method. This method is widely accepted as a scientific consensus-building method to seek experts’ opinions regarding a particular issue [20,21,22]. As multiple studies regarding death pronouncement have previously been reported, it was considered that interactive discussions among panel members could generate novel findings, for which the modified Delphi method was suitable compared with other techniques, including the Delphi method.
Expert panel selection
All panel members were recruited using purposive sampling and snowball sampling [21]. The panel members were selected nationwide through consensus among the researchers to ensure heterogeneity in terms of age, organization, and years of clinical and professional experience and expertise. Since we considered that nurses play an essential role in bereavement care, before and after the delivery of the death pronouncement, and since they are considered to be essential members of multidisciplinary care teams, we included them in the Delphi survey. We recognized the importance of involving patient representatives and medical education professionals on this subject. However, as to be a specialist in death pronouncement, we thought that patient representatives and medical education professionals may not be appropriate, therefore, we decided to seek the opinions of patient representatives and medical education specialists during the consensus meeting mentioned below.
The inclusion criteria were physicians and nurses who 1) were involved in end-of-life care and death pronouncement in daily practice and 2) had experienced death pronouncement practice for 50 or more patients. The exclusion criteria were persons who were mentally unstable or had psychological conditions which made them unsuitable for participation in the research (e.g., past traumatic experiences related to bereavement).
Although panel member size for the Delphi method varies in the literature, it is generally recommended to have at least 20 members [20,21,22]. Considering a response rate of approximately 80% based on previous studies, the minimum recruitment number was 25 [23].
Delphi process
First, we performed a thorough narrative literature review and developed a draft version of the competencies and EPAs item list. This was because we thought that to effectively train younger physicians, the defined competencies alone were not sufficient for on-site clinical education and that specific actions (EPAs) were also necessary [16, 24]. In other words, we thought EPA is a much easier concept for practitioners to conceptualize than invisible competencies [17]. Since this study’s focus was on physicians in a residency training program, the general ward of hospitals, where most physicians work, was the targeted setting.
Second, we constructed a web-based questionnaire using Google Forms®, posted the draft version of the item list. Prior to conducting the survey, we conducted a pilot survey with three physicians and four nurses who met the eligibility criteria, and modified the questionnaire based on its results. The panel members were asked to respond to each item using a 5-point Likert scale to provide their opinion on whether an item should be included in the list. The response options were 1 (should definitely be excluded), 2 (should be excluded), 3 (neither), 4 (should be included), and 5 (should definitely be included). In addition, there was a free text option for the panel members to make suggestions regarding any modification in wording or addition of other items. The web URL of the questionnaire was sent via e-mail to the panel members, and they were asked to answer the questionnaire independently.
Revisions to the items were made according to the panel members’ responses and discussion among researchers. Based on previous literature [20,21,22,23], and discussion within the research team, the consensus criteria to retain items from the draft list were set as 1) average of 4 points or higher on the 5-point Likert scale and 2) more than 80% of the panel members rating it as 4 or 5. When the consensus criteria had been met and no more significant comments emerged, the researchers discussed and decided more rounds were not required. To ensure anonymity and autonomous response, the list of panel members was blinded among the members and responses were assigned individual codes.
A consensus meeting was held in a non-anonymous face-to-face web conference with three additional external evaluators, including a patient representative, resident physician, and medical education professional, to assess the face validity of the list of items developed through the first and second Delphi rounds. We considered that the participation of patient representatives who underwent death pronouncement delivery, resident physicians who were the focused target of this study, and medical education professionals who would be the users of output from this study as essential for this research, and we invited them using the purposive sampling method. After the consensus meeting, the final version of the item list was developed through a third Delphi round with the attendees of the consensus meeting. Additionally, we created a draft of the matrix of competencies and EPAs, which was examined during the meeting. Then, the matrix, after minor modifications, was presented again after the third round via an e-mail to the attendees of the meeting, and was then finalized.
Statistical analysis
Descriptive statistics were used to summarize the data using JMP version 15.0 software (SAS Institute, Cary, NC, USA).
Ethics approval and consent to participate
The research protocol for this study was approved by University Institutional Review Board (approval number: A191100009). All panel members and external evaluators, including a patient representative, were given a sufficient explanation of the research intent in advance, and written consent to participate in the research was obtained from all participants.