- Research article
- Open Access
- Open Peer Review
Palliative care training addressed to hospital healthcare professionals by palliative care specialists: a mixed-method evaluation
BMC Palliative Care volume 18, Article number: 88 (2019)
Despite the great advances in the concept of palliative care (PC) and its benefits, its application seems to be delayed, leaving unfulfilled the many needs of patients and family members. One way to overcome this difficulty could be to develop a new training programme by palliative care specialists to improve PC primary skills in healthcare professionals. The aim of this study was to evaluate the training’s impact on trainees within a hospital setting using Kirkpatrick’s and Moore’s models.
We adopted a mixed-method evaluation with concurrent triangulation. The evaluation followed the first three steps of Kirkpatrick’s and Moore’s models and included a pre- and post-training evaluation through self-administered questionnaires and focus groups. We used the McNemar statistical test.
The results highlighted the significant amount of knowledge acquired by the hospital professionals after training, in terms of increasing their knowledge of palliative care and in terms of the change in meaning that they attributed to phenomena related to chronicity and incurability, which they encounter daily in their professional practice. In both quantitative and qualitative research, the results, in synthesis, highlight:
(i) the development of a new concept of palliative care, centred on the response to the holistic needs of people;
(ii) that palliative care can also be extended to non-oncological patients in advanced illness stages (our training was directed to Geriatrics and Nephrology/Dialysis professionals);
(iii) the empowerment and the increase in self-esteem that healthcare professionals gained, from learning about the logistical and structural organization of palliative care, to activate and implement PC;
(iv) the need to share personal aspects of their professional life (this result emerges only in qualitative research);
(v) the appreciation of cooperation and the joining of multiple competences towards a synergistic approach and enhanced outcomes.
It is necessary to further develop rigorous research on training evaluation, at the most complex orders of the Kirkpatrick and Moore models, to measure primary PC skills in health care professionals. This will develop the effectiveness of the integration of I- and II-level palliative care competencies in hospitals and improve outcomes of patients’ and families’ quality of life.
Palliative care (PC) is a complex aspect of end-of-life (EoL) treatment, which focuses on providing compassionate medical care and preserving the patient’s dignity throughout the unfolding of a disease [1, 2]. Data from the literature largely confirm the effectiveness of PC [3,4,5,6,7] and encourage early access of patients to PC as well as the integration of PC into standard care [8,9,10,11]. Nonetheless, national- and international-level data  evidence the low referral rate of patients to PC . This may most likely be due to sustainability issues, as PC requires ever more qualified PC specialists for a steadily growing patient supply and dwindling economic resources.
Moreover, the implementation of PC is not straightforward, as it implicates a broad range of aspects – from QoL to EoL interventions, from human relations to treatment costs [14,15,16,17]. Currently, the “modern” PC specialist is called on to cover multiple roles: being at the same time a clinician, a trainer (especially in the hospital setting) and a researcher with a natural attitude towards quality improvement . However, it is unrealistic that PC experts meet all PC needs of incurable patients [14, 18].
One way to overcome such difficulties could be, as proposed by Quill and Abernethy , to structure PC on two levels: a I-level, so-called generalist PC, intended to meet the patient’s basic needs for PC in primary care and within hospital wards and involving transversal skills and knowledge common to all health professionals (HPs) in their daily clinical activity. The II-level is set up for more complex physical, psychological, social or spiritual needs and is carried out by specialized PC professionals . The model, however, appears not to have been implemented so far, and there is still no indication of pursuing it in practical terms.
Some authors underline the importance of activating training courses to improve I-level skills among non-specialized PC professionals on basic principles of palliative care and to implement cooperation between the I and II levels [11, 14, 19].
Although the literature does describe several training interventions in PC [20,21,22,23], unfortunately, it rarely reports information about assessment tools used  or the methodological validity. A recent review by Turrillas et al.  has recognized an enormous lack of evidence for PC training evaluation.
In most cases, evaluation of training is mostly based on participant satisfaction and knowledge learning. A rigorous method is mandatory to evaluate the impact of a training course, according to the Medical Research Council framework (MRC) for complex intervention . Nonetheless, the literature on this rigorous method is still underdeveloped [27, 28]. Accordingly, the aims of this study were to evaluate, both quantitatively and qualitatively, training’s impact on trainees while assessing the training’s model and evaluation method. For this study, we chosen to focus on hospital wards.
The study intends to make an important contribution by using a rigorous method for training evaluation in PC and to fill a gap in knowledge/education on PC for hospital healthcare professionals.
We adopted a mixed-method evaluation with the concurrent triangulation, which consists of a qualitative and quantitative collection of data in the same period, in one subsequent separate analysis and, finally, in a comparison of the outcomes [29, 30].
We decided to carry out a before-after evaluation of the training, focusing on Moore  third order of learning, which is articulated in 3A (declarative knowledge) and 3B (procedural knowledge).
We developed a new training programme for PC based on the Kirkpatrick model [32, 33] and its elaboration by Moore . The training programme, lasting 4 h in two different editions to facilitate participation, was taught by II-level PC specialists to HPs of all departments (I-level). The training focussed on the vision of PC by the World Health Organization (WHO) , the purpose of a PC unit in the hospital and the sharing of PC needs in hospital wards [7, 34].
Context and sampling
The study was performed at the General Hospital “Arcispedale Santa Maria Nuova”, a 900-bed public hospital, located in Reggio Emilia, a town in northern Italy, recently awarded the title of Clinical Cancer Centre by the Organization of European Cancer Institutes (OECI). In the hospital, there is a Palliative Care Unit (PCU) assigned to provide specialist consultations for patients (and patients’ family members) both hospitalized in the hospital wards both afferent to the outpatient clinic. The PCU was established in April 2013 and currently includes three senior physicians, two advanced practice nurses and a specialist nurse in education.
The study sample was composed of HPs from the Radiotherapy, Geriatrics and Nephrology/Dialysis wards, who were involved in the basic PC training and who represented all professional categories implicated (physicians, nurses, technicians, biologists, etc.).
Data collection and analysis
We used an open-ended questionnaire  about the comprehension of the WHO definition of PC, administered before and after training, asking: ‘Referring to your professional experience, what do you think are the goals and characteristics of PC?’. We analysed data using a framework constructed by Beccaro et al. , which is based on the 16 domains characterizing the WHO definition of PC. We calculated the percentages for each domain before and after training, along with the relevant 95% bilateral confidence intervals, constructed according to the Clopper-Pearson method. Pre- and post-training percentages were compared with the McNemar test; a p-value < 0.001 was considered statistically significant. The analysis was conducted using R3.3 (R Foundation for Statistical Computing, Vienna, Austria).
Qualitative feedback on PC knowledge and learning was gathered by means of focus groups (FGs) that served to encourage interaction between the participants, elicit a range of opinions/views and generate a discussion on the topic . For each ward, we planned to conduct separate FG meetings for physicians and other HPs’ roles to bring out issues and topics characteristic of each professional profile. A moderator and an observer were present during every FG.
The qualitative analysis adopted the framework method described by Gale et al. . We concentrated the analysis on emerging themes but also on emotions and meanings that the professionals attributed to their statements. In doing so, we could search for any possible changes in meanings attributed to that phenomenon from before to after the training. The overall process was supervised by an external expert of qualitative methodology.
We finally performed data triangulation to compare the quantitative and qualitative results .
The study included 80 HPs, accounting for 59.45% of the total staff of the 3 departments considered. Of these, 19 were physicians (Ph), 47 nurses (N) or technicians (T), and 14 other professional figures, such as nurse assistants and biologists. Of these, 33 participated in the pre-training FG and 29 in the post-training FG. Besides, we collected 77 pre-training and 77 post-training questionnaires as the same participants who filled both the questionnaires. We synthesized the training participants’ characteristics and their participation in the training course in Table 1.
The open-ended questionnaire (before and after the intervention) gathered 77 different responses. Table 2 illustrates percentages, before and after, with confidence intervals and the outcome of the McNemar test  and the p-values for each domain.
All 16 domains had entries among participants’ answers except for D13. The most significant difference was observed for domain D01 “Improvement of patient QoL”, which evidenced a statistically significant difference (p-value = < 0.001) between pre- and post-training, with an approximately three-fold increase.
Two other domains also showed significant enrichment with training: D14 “Early applicability in illness path” (p-value = < 0.001) and D08 “Addressing patient and family needs” (p-value = < 0.001).
The domains that concern addressing the patient’s holistic conception and taking charge of all its dimensions (D06 “Psychosocial aspects of patient care” and D07 “Spiritual aspects of patient care”) had significantly higher representation after the training intervention (p-value = < 0.001). These results also confirm that these domains had been properly learned during the course. These domains were followed in representation by D05 “Treatment of physical symptoms” (D05) (p-value = 0.001), which doubled after training; D12 “Team approach in addressing needs” (p-value = 0.006); and D10, referring to extending care to patients’ families, “Helping family to cope with their bereavement” (p-value = 0.016).
Finally, the D02 domain “Address the problems associated with incurable diseases”, with p-value = 0.052, and D09 “Encouraging patients to live as actively as possible”, had borderline statistical significance p-value = 0.077.
The significant differences between pre- and post-intervention were suggestive of changes in the understanding of the topics, increased awareness or acquisition of new notions.
The analysis of the FGs before and after training led us to identify five overarching themes (Table 3): (1) Relationships among I- and II-levels, (2) Communication with patients and their families, (3) Clinicians’ competences in EoL care, (4) Integration among I- and II-levels, and (5) Self consideration of their emotions. These themes emerged with different meanings (defined within the sub-themes) in relation to pre-training and post-training data collection. We highlighted this meaning shift in Table 3.
Theme 1. Relationships between I- and II-levels, passing from obstacles to synergies
As the first result of the training, the meanings shifted from what we denominated “doubt and disagreement” to “knowledge and synergy”. Before the training, the HPs primarily emphasized a lack of specific guidance on PCU activities. They expressed the need to receive basic relevant information on PC, especially its objectives and its procedure, to advice a patient and her/his family about PC provision. The major deterrent was represented by the moment of the patient’s discharge from the hospital to hospice or home care. HPs revealed they needed information about how activate PC provision after hospitalization.
“There needs to be clarity on the figures of reference for health professionals and PCU, the goals of PC, and how PCU works” (FG 3 Ph).
“One of the doubts I have is on when to call in palliative-care medical advice” (FG 1 Ph).
Furthermore, there does not appear to be an official agreement indicating which hospital specialist is responsible for PC patient management. This not only creates obvious delays in requesting and providing assistance but also involves a conflicting decision-making process about treatments. Physicians and nurses, within the same wards, often disagreed on treatments. Participants were not fully aware of the local network, while they were aware of the weakness and the precariousness of their therapeutic programme, mainly when carried out at the patient’s home. HPs saw the risk that the continuity of care might disappear.
“Our opinion was to suspend the treatment since the chances (of survival) were very few, but the specialist wanted to try a last line anyway, despite the patient … being already in desperate conditions. So there is no agreement between us” (FG 1 Ph).
“This is a problem that doctors often cause us … . They often demand things that are impossible to achieve” (FG 2 N).
Once the hospital professionals received training on PC, they became aware of the broader picture and organization of PC, the paths for pursuing its integration within daily hospital activity and its implementation outside hospital structures. Additionally, having a better comprehension of the roles and profiles of the professionals working in this service allowed the other hospital professionals to be more attentive and sensitive in facilitating palliative doctor consultancies.
“It was useful to get a clear definition of the meaning of palliative care, in relation to care and professional roles with them (PCU staff)” (FG 7 Ph).
Having clarified that PC needs can actually be met by the PC specialist once a PC plan is activated led the participants to feel a sense of synergy with colleagues that seemed to facilitate inter-professional relations. The presence of the palliative specialist helped trainees to achieve a new perspective.
“Now, after the training, there is a lot more awareness (on PC), and we can work in line with the medical staff, whereas before, when we had a patient in pain, we were in a situation where no one would take on the final provision for the treatment” (FG 8 N).
“With the introduction of the palliative doctor, we are facilitated in the assistance and decision making by coordination with the palliative doctor” (FG 11 Ph).
Theme 2. Communication with patient and family: ‘a collaborative approach to manage communication’
The relationship and communication with the patient’s family were reported as particularly strenuous by the professionals. Among the aspects highlighted by the participants were dealing with suffering and incurable conditions, the nature of the information they are in charge of communicating (e.g., poor prognosis, recurrent disease, last line of active treatment, transition from active care to PC) and the underlying issues of communication skills and personal ethics.
“I'm faced with the dilemma: “What should we communicate and how?” “I sometimes ask myself whether I should communicate the diagnosis or not” (FG 7 Ph).
“Since I do not know what the patient's wishes are, I often refer to the family's judgement” (FG 7 Ph).
“Each of us is self-taught in this field, but in reality, there are communication techniques that we absolutely do not know; we lack communication training” (FG 1 Ph).
Participants felt that communication with the family was very problematic and listed some typical situations, such as when the family members cannot accept the fact their relative’s disease is inevitably worsening towards death or when a family member asks to continue a useless therapy.
“It is necessary to help the family understand the meaning of pain therapy in relation to the process of accompanying the patient towards death; many times, the medical staff is forced to resort to a defensive medicine, just because the family are not entirely convinced that this person, in the end, is dying” (FG 5 Ph).
They stressed that this issue remained a critical point despite having undergone the present training course and began planning further training that could help them address their communication needs towards a collaborative approach with PC professionals.
“It is important to organize the approach together with colleagues, with the patient and his/her family, a possible caregiver” (FG 1 Ph).
“Our problems with communication lie largely in the lack of training” (FG 3 Ph).
Theme 3. Clinicians’ competences in EoL care: ‘becoming competent clinicians of the EoL’
Participants shifted from what we called “sense of uselessness towards the EoL” to “discovering the ‘treatments’ of the EoL”. In fact, participants felt a sense of uselessness, of ‘having their hands tied’. Before the training, pain was a cause of conflict among nurses and physicians: on one hand, the physicians considered the problem of the patient’s pain already solved, while the nurses thought there was a lack of pain therapy culture. Participants were more sensitive to the patient’s global suffering:
“The problem is precisely the therapy of pain, which perhaps we have not yet understood how it should be done, we see the patient suffering, but sometimes we have our hands tied” (FG 4 N).
“We often ask family members to allow us to give (PC) a try, … for something that will probably prolong the patient's suffering and that brings no apparent advantage to the patient's well-being. So, there is an insecurity that we all have towards these choices” (FG 1 Ph).
The participants discovered the importance of EoL treatments, as they reported a higher sensitivity and attention to the patient at the EoL after training. Nurses recognized that physicians, after the training, were more likely to involve palliative doctors, when before they felt more embarrassed. All the HPs gained a clear understanding of the area of intervention of PC, namely, the response to the needs of the person, even when they could no longer manage the treatment of the disease.
Nevertheless, the problem of identifying psychosocial and spiritual needs remained in both the pre- and post-training FGs.
Participants understood that the intervention of the PC specialist is needed to address the complexity and multiplicity of symptoms and needs that cause suffering in the patient.
“Surely our doctors have become confident enough to call the palliative doctor, and this alone is an important step ahead” (FG 10 N).
“For our work, we should have a greater knowledge of what palliative care is” (FG 9 Ph).
Theme 4. Integration between I- and II-levels: ‘a possible integrative model with the PC Unit’
From the “initial perception of the impossibility of meeting and integrating the PC specialists” and being somewhat powerless, participants shifted to an “understanding of the process, which will facilitate PC inclusion in their work”. In fact, the first reaction of the professionals revealed their doubts about the feasibility of PC. The expectations of participants before the training were to receive not only theoretic notions but also concrete proposals they could transfer to the patient’s bedside. The first obstacle was traced back to organizational problems. HPs declared that working schedules were short and that the organization often did not allow a method that was different from the one traditionally intended, where it is the doctor alone who interacts with the patient and the family. Participants thought that more complex approaches, such as those proposed by palliative specialists involving several actors, were challenging to apply.
“I am often involved in the most difficult part of setting up the PC programme and coordinating everyone, from my colleagues to the patient, family, and a possible caregiver” (FG 1 Ph).
“Even doctors, however, are always struggling to involve the palliative doctors. They always wait until the last moment” (FG 4 N).
The participants’ understanding of the organization within the PCU seemed to have facilitated the involvement of the palliative doctor’s consultancies within the care. Participants became aware of the practical possibility of activating PC and showed the need for greater integration of PC specialists within the examined operating units (OUs).
“We should involve palliative specialists more and more, so they can get to know our patients, the dynamics at our department, and grasp the mesh of our organization” (FG 9 Ph).
Still, some HPs perceived organizational boundaries and constraints.
“What we will discover is whether we can implement PC on a practical basis, with the patient. However, in this setting, there is neither the time nor the mindset to use this approach to the patient. Because we are unable to do it... because of the organization” (FG 3-4 N & Ph).
Theme 5. Self-consideration of their emotions: ‘training course to support professionals’
The last theme emerging from FGs regarded the difficulty of the professionals in sustaining, over time, the emotional charge of daily contact with patients and families who have EoL situations.
Following training, professionals in the FGs recognized above all the need to receive psychological support themselves to face complex EoL situations.
“Plus, we don't receive much attention ourselves. In fact, the staff suffer... from an emotional point of view. You deal with it on your own. You can take an individual route, but it's not enough. For years we've been claiming that we need support for the staff” (FG 2 N).
The risk of burden was perceived especially by nurses, who felt they would gradually become unable to help anymore because of the intensity of emotions experienced. HPs reported that they were not able to identify, welcome and process those strong feelings. Both personal development and preparedness were needed to cope with the phenomenon.
“Manage this impact requires the right maturity, and the right preparation; the psychological aspect is important for the family, it is important for the doctor, but it is also important for the nurse and the assistants who are in contact with the patient on a daily basis” (FG 2-6 N & T).
From the post-training FG, the previously highlighted needs and the fears expressed by the participants related to the risks of emotional stress led the way to a precise awareness. It appeared that the requests for help became explicit, even if not yet well circumstantiated: from training to communication to the care for HPs, to emotional support in the management of complex cases. Participants recognized the training as an occasion for discussion and sharing of the most complex problems. The shared search for common solutions could become a support strategy.
“We should establish a mutual-support group. Moments to dedicate not only to the discussion of cases but also of what has caused emotional reactions in the colleagues” (FG 8 -12 N & T).
The participants were very active and participatory in the whole path of training and research, allowing the collection of very interesting data in both our quantitative and our qualitative research. The triangulation of data led, in most cases, to both confirmatory and novel results.
The results obtained highlighted the significant amount of knowledge acquired by the participants after training, in terms of increasing the knowledge on PC and in terms of the change in meaning that they attributed to phenomena related to chronicity and incurability, which they encounter daily in their professional practice.
In both quantitative and qualitative research, the results, in synthesis, highlight:
the development of a new concept of PC, centred on the response to the holistic needs of people (Domains: D06, D07, D08 and Theme 3);
the understanding that PC can also be extended to non-oncological patients in advanced illness stages (our training was direct to Geriatrics and Nephrology/Dialysis professionals);
the empowerment and increased self-esteem that HPs gained, from learning about the logistical and structural organization of PC, to activate and implement PC (Domains: D01, D014, Theme 1, 3 and 4);
the need to share personal aspects of their professional life (this result emerged only in the qualitative research: Theme 5);
the appreciation of cooperation and the joining of multiple competences towards a synergistic approach and enhanced outcomes (Domain: D012 and Theme 4).
The present work describes the piloting of a new training programme along with its evaluation.
This study evaluates a basic PC training programme in a hospital by means of a fittingly rigorous methodology, in view of implementing the II-level PC model dealing with patients who are candidates for PC.
The adoption of the validated models of Kirkpatrick and Moore and a mixed-method approach allowed us to explore the phenomenon of PC as a whole. In particular, through quantitative data, we evaluated the increase in awareness, while the emerged meaning shift revealed both what the participants learned and how they signified what they learned.
In agreement with Schenker and Arnold [18, 38, 39], to improve PC for patients with chronic illness, we used specific training to develop I-level PC skills in HPs to improve the quality of care in hospital. Our results are in agreement with other studies that were also applied in non-oncological settings, for example, those obtained by Hepgul et al. , which emphasized that the collaboration between neurologists and palliative care professionals has a positive overall impact on the management of patients with progressive neurological disorders. Similar results were obtained by Bowman and Meier  in chronic obstructive pulmonary disease and Riegel and Kimmel  in end-stage heart disease.
The results obtained highlighted the significant amount of knowledge acquired by the participants after training, in terms of increasing their knowledge of PC and in terms of the change in meaning that they attributed to phenomena related to chronicity and incurability, which they encounter daily in their professional practice . Turrillas et al. , through a systematic review of the existing literature on the subject, showed that in the analysed studies, despite the use of various original or modified educational training and assessment methods of which psychometric characteristics were often not reported, all educational methods have allowed non-palliative care professionals to improve their knowledge and preparation regarding palliative care and EoL patient management.
In our study, the qualitative analysis showed that meaning shifts emerged both as an interesting result of the training and as an innovative proposal for training evaluation.
Our training course has helped the HPs (i) develop a new concept of PC centred on the response to the needs of people  and not only to care; (ii) understand that PC can also be extended to non-oncological patients [44, 45] in advanced illness stages; (iii) gain empowerment and increased self-esteem from learning about the logistical and structural organization of PC to activate and implement PC [46,47,48]; (iv) appreciate the need to share personal aspects of their professional life; (v) appreciate the cooperation and joint multiple competences that enable a synergistic approach and enhanced outcomes [7, 49].
Both HPs and PC specialists mentioned throughout the course their need for multidisciplinary team support to improve care processes; the need to work together emerged, as did the need to share choices and to promote integration among the various kinds of professionals .
These unmet needs, which all fall under the umbrella of PC in the hospital setting, were eventually summarized in the request for immediate development of additional training modules, one for each specific topic/unmet need, such as management of personal emotions , communication skills for delivering bad news to patients and their families , and holistic patient management . In fact, after this study, participants requested that training boards organize a course that could deepen their knowledge on psycho-social needs and advanced training in bad-news communication for physicians, while the PC Unit has recently begun a new qualitative study on spiritual needs in chronic illness patients.
This study has some limitations. The number of questionnaires collected was not high, although the statistical analysis allowed us to identify significant differences. We measured only the impact on professional competencies and not effectiveness on patients and health outcomes.
There is a growing need to implement new PC training delivery models . We wanted to experiment with the model in which PC specialists (II-level) help hospital clinicians develop I-level skills through a training course, and the results were rigorously measured.
This study intended to propose a training evaluation method that used both quantitative and qualitative data; this method could also be applied to other training courses. However, it will be necessary to go beyond the learning of applicable knowledge and new meanings to propose training that develops measurable skills in professionals, as well as outcomes to improve patients’ and families’ QoL. It is necessary to conduct further rigorous research on the training evaluation, at the most complex orders of the Kirkpatrick and Moore models, to measure the effectiveness of the integration of I- and II-level PC competencies in care pathways and to evaluate patient- and family-related outcomes.
Availability of data and materials
The study documentation is collected and managed by the coordinator of the study centre (PC Unit, AUSL – IRCCS di Reggio Emilia), and datasets are available on reasonable request.
Medical Research Council
Organization of European Cancer Institutes
Palliative Care Unit
Quality of Life
World Health Organization
World Health Organization. Cancer: WHO definition of palliative care. 2019. http://www.who.int/cancer/palliative/definition/en/. Accessed 27 May 2019.
World Health Assembly. Strengthening of palliative care as a component of integrated treatment throughout the life course: report by the secretariat. Geneva: Institutional Repository for Information Sharing, World Health Organization; 2014. http://www.who.int/iris/handle/10665/158962A67_31-en.pdf?sequence=1&isAllowed=y. Accessed 29 May 2019
Hui D, Kim SH, Roquemore J, Dev R, Chisholm G, Bruera E. Impact of timing and setting of palliative care referral on quality of end-of-life care in cancer patients. Cancer. 2014;120:1743–9.
Smith TJ, Temin S, Alesi ER, Abernethy AP, Balboni TA, Basch EM, et al. American society of clinical oncology provisional clinical opinion: the integration of palliative care into standard oncology care. J Clin Oncol. 2012;30:880–7.
Higginson IJ. Making palliative care matter. J Palliat Med. 2014;17:1292–3.
Hui D, Bruera E. Integrating palliative care into the trajectory of cancer care. Nat Rev Clin Oncol. 2016;13:159–71.
Hepgul N, Gao W, Evans CJ, Jackson D, van Vliet LM, Byrne A, et al. Integrating palliative care into neurology services: what do the professionals say? BMJ Support Palliat Care. 2018;8:41–4.
Zimmermann C, Swami N, Krzyzanowska M, Hannon B, Leighl N, Oza A, et al. Early palliative care for patients with advanced cancer: a cluster-randomised controlled trial. Lancet. 2014;383:1721–30.
Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, et al. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med. 2010;363:733–42.
Bakitas MA, Tosteson TD, Li Z, Lyons KD, Hull JG, Li Z, et al. Early versus delayed initiation of concurrent palliative oncology care: patient outcomes in the ENABLE III randomized controlled trial. J Clin Oncol. 2015;33:1438–45.
Costantini M. Sfide e opportunità delle cure palliative moderne. Bologna: ASMEPA Edizioni; 2017.
De Lima L, Pastrana T. Opportunities for palliative care in public health. Annu Rev Public Health. 2016;37:357–74.
Hawley P. Barriers to access to palliative care. Palliat Care. 2017;10:1178224216688887.
Quill TE, Abernethy AP. Generalist plus specialist palliative care--creating a more sustainable model. N Engl J Med. 2013;368:1173–5.
Tuca A, Gomez-Martinez M, Prat A. Predictive model of complexity in early palliative care: a cohort of advanced cancer patients (PALCOM study). Support Care Cancer. 2018;26:241–9.
May P, Garrido MM, Cassel JB, Kelley AS, Meier DE, Normand C, et al. Cost analysis of a prospective multi-site cohort study of palliative care consultation teams for adults with advanced cancer: where do cost-savings come from? Palliat Med. 2017;31:378–86.
Duckett S. Aligning policy objectives and payment design in palliative care. BMC Palliat Care. 2018;17:1–10.
Schenker Y, Arnold R. The next era of palliative care. JAMA. 2015;314:1565–6.
Block SD, Billings JA. A need for scalable outpatient palliative care interventions. Lancet. 2014;383:1699–700.
Kadlec H, Hollander MJ, Clelland C, Kallstrom L, Hollander M. Family physicians enhance end-of-life care: evaluation of a new continuing medical education learning module in British Columbia. BMC Med Educ. 2015;15:119.
Beccaro M, Gollo G, Ceccon S, Giordano M, Salvini E, Vignali S, et al. Students, severe illness, and palliative care: results from a pilot study on a school-based intervention. Am J Hosp Palliat Care. 2015;32:715–24.
Bassah N, Cox K, Seymour J. A qualitative evaluation of the impact of a palliative care course on preregistration nursing students’ practice in Cameroon. BMC Palliat Care. 2016;15:37.
Pype P, Mertens F, Wens J, Stes A, Van den Eynden B, Deveugele M. Preparing palliative home care nurses to act as facilitators for physicians’ learning: evaluation of a training programme. Palliat Med. 2015;29:458–63.
Vindrola-Padros C, Mertnoff R, Lasmarias C, Gomez-Batiste X. Palliative care education in Latin America: a systematic review of training programs for healthcare professionals. Palliat Support Care. 2018;16:107–17.
Turrillas P, Teixeira MJ, Maddocks M. A Systematic review of training in symptom management in palliative care within postgraduate medical curriculums. J Pain Symptom Manage. 2019;57:156–70.e4.
Campbell NC, Murray E, Darbyshire J, Emery J, Farmer A, Griffiths F, et al. Designing and evaluating complex interventions to improve health care. BMJ. 2007;334:455–9.
Becker G, Momm F, Deibert P, Xander C, Gigl A, Wagner B, et al. Planning training seminars in palliative care: a cross-sectional survey on the preferences of general practitioners and nurses in Austria. BMC Med Educ. 2010;10:43.
Ferrell B, Virani R, Paice JA, Coyle N, Coyne P. Evaluation of palliative care nursing education seminars. Eur J Oncol Nurs. 2010;14:74–9.
Zhang W, Creswell J. The use of “mixing” procedure of mixed methods in health services research. Med Care. 2013;51:e51–7.
Creswell JW, Creswell JD. Research design: qualitative, quantitative, and mixed methods approaches. Thousand Oaks: Sage Publications; 2003.
Moore DE Jr, Green JS, Gallis HA. Achieving desired results and improved outcomes: integrating planning and assessment throughout learning activities. J Contin Educ Heal Prof. 2009;29:1–15.
Kirkpatrick JD. Implementing the four levels: a practical guide for effective evaluation of training programs. San Francisco: Bernett-Koehler Publisher; 2007.
Kirkpatrick JD, Kirkpatrick W. Kirkpatrick’s four level of training evaluation. Alexandria: ATD Press; 2016.
Eddy K, Jordan Z, Stephenson M. Health professionals’ experience of teamwork education in acute hospital settings: a systematic review of qualitative literature. JBI Database System Rev Implement Rep. 2016;14:96–137.
Di Leo S, Beccaro M, Finelli S, Borreani C, Costantini M. Expectations about and impact of the liverpool care pathway for the dying patient in an italian hospital. Palliat Med. 2011;25:293–303.
Addington-Hall JM, Bruera E, Higginson IJ, Payne S. Research methods in palliative care. Oxford: Oxford University Press; 2007.
Gale NK, Heath G, Cameron E, Rashid S, Redwood S. Using the framework method for the analysis of qualitative data in multi-disciplinary health research. BMC Med Res Methodol. 2013;13:117.
Schenker Y, Arnold R. Toward palliative care for all patients with advanced cancer. JAMA Oncol. 2017;3:1459–60.
Schenker Y, Arnold R. Possible underestimation of the provision of palliative care-reply. JAMA Oncol. 2018;4:886.
Bowman B, Meier DE. Palliative care for respiratory disease: an education model of care. Chron Respir Dis. 2018;15:36–40.
Riegel B, Kimmel SE. Palliative care: is now the time? Eur J Cardiovasc Nurs. 2018;17:474–6.
Carroll T, Weisbrod N, O'Connor A, Quill T. Primary palliative care education: a pilot survey. Am J Hosp Palliat Care. 2018;35:565–9.
Kassianos AP, Ioannou M, Koutsantoni M, Charalambous H. The impact of specialized palliative care on cancer patients’ health-related quality of life: a systematic review and meta-analysis. Support Care Cancer. 2018;26:61–79.
Rosansky SJ, Schell J, Shega J, Scherer J, Jacobs L, Couchoud C, et al. Treatment decisions for older adults with advanced chronic kidney disease. BMC Nephrol. 2017;18:200.
Gatta B, Turnbull J. Providing palliative care in the medical ICU: a qualitative study of MICU physicians’ beliefs and practices. Am J Hosp Palliat Care. 2018;35:1309–13.
Dudley N, Ritchie CS, Rehm RS, Chapman SA, Wallhagen MI. Facilitators and barriers to interdisciplinary communication between providers in primary care and palliative care. J Palliat Med. 2019;22:243–9.
Abedini NC, Chopra V. A model to improve hospital-based palliative care: the palliative care redistribution integrated system model (PRISM). J Hosp Med. 2018;13:868–71.
Hui D, Hannon BL, Zimmermann C, Bruera E. Improving patient and caregiver outcomes in oncology: team-based, timely, and targeted palliative care. CA Cancer J Clin. 2018;68:356–76.
Brown CR, Hsu AT, Kendall C, Marshall D, Pereira J, Prentice M, et al. How are physicians delivering palliative care? A population-based retrospective cohort study describing the mix of generalist and specialist palliative care models in the last year of life. Palliat Med. 2018;32:1334–43.
Rosenblum AM, Chasen MR. Palliative care: who is responsible? J Natl Compr Cancer Netw. 2018;16:791–2.
Mills J, Wand T, Fraser JA. Exploring the meaning and practice of self-care among palliative care nurses and doctors: a qualitative study. BMC Palliat Care. 2018;17:63.
Gorniewicz J, Floyd M, Krishnan K, Bishop TW, Tudiver F, Lang F. Breaking bad news to patients with cancer: a randomized control trial of a brief communication skills training module incorporating the stories and preferences of actual patients. Patient Educ Couns. 2017;100:655–66.
Li L, Sloan DH, Mehta AK, Willis G, Weaver MS, Berger AC. Life perceptions of patients receiving palliative care and experiencing psycho-social-spiritual healing. Ann Palliat Med. 2017;6:211–9.
Tanzi S, Di Leo S, Mazzini E, Castagnetti M, Turrà C, Peruselli C, Costantini M. Long-term sustainability of a quality improvement program on cancer pain management: a complex intervention in an inpatient setting. Tumori. 2019;Aug:1–8.
The Authors wish to thank all the healthcare professionals who kindly participated in this study giving their time, experience, and insights. Finally, the Authors are grateful to Manuella Walker (Pisa, Italy) for the support in editing the paper.
The present research was performed independently and did not receive any internal or external funding.
Ethics approval and consent to participate
The study was approved by the Provincial Ethics Committee of Reggio Emilia (n 2016/0019236) and conducted according to the Declaration of Helsinki; all participants signed a written informed consent.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Artioli, G., Bedini, G., Bertocchi, E. et al. Palliative care training addressed to hospital healthcare professionals by palliative care specialists: a mixed-method evaluation. BMC Palliat Care 18, 88 (2019) doi:10.1186/s12904-019-0476-8
- Palliative care
- Training evaluation
- Health care professionals
- Palliative care specialists
- Educational models