key: cord-0784283-dx6grrrr authors: Rosenberg, Abby R.; Barton, Krysta; Junkins, Courtney; Scott, Samantha; Bradford, Miranda C.; Steineck, Angela; Lau, Nancy; Comiskey, Liam; Yi-Frazier, Joyce P. title: Creating a Resilient Research Program – Lessons Learned from a Palliative Care Research Lab date: 2020-07-01 journal: J Pain Symptom Manage DOI: 10.1016/j.jpainsymman.2020.06.033 sha: 20c77c6a88309b748e1df918361e60b5f348ca62 doc_id: 784283 cord_uid: dx6grrrr Conducting palliative care research can be personally and professionally challenging. While limitations in funding and training opportunities are well-described, a less recognized barrier to successful palliative care research is creating a sustainable and resilient team. In this special report, we describe the experience and lessons-learned in a single palliative care research lab. In the first few years of the program, 75% of staff quit, citing burnout and the emotional tolls of their work. To address our sustainability, we translated resilience theory to practice. First, we identified and operationalized shared mission and values. Next, we conducted a resilience resource needs assessment for both individual team-members and the larger team as a whole, and created a workshop based curriculum to address unmet personal and professional support needs. Finally, we changed our leadership approach to foster psychological safety and shared mission. Since then, no team-member has left and the program has thrived. As the demand for rigorous palliative care research grows, we hope this report will provide perspective and ideas to other established and emerging palliative care research programs. The demand for palliative care "science" is emerging rapidly. In the past decade, the number of peerreviewed palliative care publications has expanded exponentially, several dedicated and successful palliative care research organizations have been established, interest in funding palliative care research and training has grown, and national organizations have established academic meetings focused specifically on palliative care science. (1) (2) (3) (4) (5) (6) Despite its importance, conducting palliative care research is challenging. Limitations in both funding and research training opportunities are well-described. (6) (7) (8) (9) A less-recognized barrier to palliative care research, however, is that of creating a sustainable research team. Just as a palliative care clinical team is inherently multidisciplinary, so too is the palliative care research team. In both settings, recognition of the shared and unique contributions of team members is necessary for success. (10) And, just as palliative care clinical practice may be inherently challenging due to the emotional exhaustion and burnout experienced by clinicians, (11) so too is the conduct of palliative care research. In both settings, attention to staff resilience is necessary. Our "Palliative Care and Resilience" research lab was founded in 2014. In its first 2 years, 3 out of 4 staff quit, citing the emotional toll of conducting palliative care research. Nearly all members of the team experienced some degree of emotional distress, anxiety, or burnout. In the ensuing years, we developed internal procedures to build team resilience and sustainability. The objective of this special report is to share our lessons-learned and strategies for improvement. Our hope is that this report provides perspective and ideas to other established and emerging palliative care research programs. Palliative care research is inherently broad and includes basic (bench) sciences, clinical and translational research, and population based epidemiologic studies. Our program focuses on clinical (patientcentered) research, and more specifically on interventions designed to build resilience, alleviate suffering, and improve quality of life. Conducting our studies involves direct contact with patients and families in the form of project coordination, survey-based data-collection, patient-and family-based interviews, and intervention delivery. Hence, our team includes diverse research staff (Clinical Research Coordinators [CRCs] and interventionists), methodologists (biostatisticians and qualitative research analysts), and both early and senior career faculty ( Table 1) . When we launched the lab, all team-members understood that our research participants would be patients who were seriously ill and family-members who might be distressed and/or bereaved. Where team-members struggled, however, was with the emotional tolls of witnessing and vicariously living with serious illness (Table 1) . Specifically, patient and family experiences reminded team-members of their own, previously suffered losses and traumas. CRCs, interventionists, and qualitative analysts who spent time working directly with patients and families shared that their built-relationships were meaningful for both themselves and the research participants. They felt unprepared to navigate processes of grief and bereavement when patients became more seriously ill or died. They mourned the loss of relationships when studies ended. Both qualitative analysts and biostatisticians who were otherwise removed from direct patient contact still reported the jarring emotional impact of observing illness and death second-hand. (12) Many of our CRCs and interventionists came into their positions with limited work experience; few had prior life experience with seriously ill patients. They reported a sense of imposition when interacting with ill or distressed patients and families ( Table 1) . They shared that not knowing if or when patients would die provoked severe anxiety. In contrast, some of our interventionists and qualitative analysts had more extensive training and life experience. For them, the challenges revolved around navigating tensions between following an intervention or interview "script" versus responding skillfully to patient or family emotions in real time. They shared that maintaining role-identity and creating professional boundaries were struggles. The stressors of early and later career investigators were often different from those of other study staff (Table 1) . Here, sources of stress tended to center on career development, including securing funding for research studies and publishing the results. Compounding these challenges were the philosophical processes of early academic careers, including establishing long-term goals and career-identities. Often for the first time, early career investigators felt responsible for their own future. Many started their careers in a clinical fields being inspired to do research based on what they observed. Now they were learning to balance clinical and research roles, responsibilities to themselves and their team, and the sense that they were in the defining moments of their career. Finally, senior investigators felt unprepared to navigate the stress of establishing and leading the research program (Table 1) . Indeed, few senior investigators have formal training or mentorship in skills such as human resources, advocacy, team-building, strategic planning, or budget management; most arrive in their leadership roles based on academic productivity and seniority. (13) (14) (15) In our case, the senior investigators were simultaneously learning to manage and support the team's emotional struggles and career development needs. The added degree of staff turn-over created challenges for budgets and productivity. Errors were made, projects were stalled, and team morale was low. Taken together, the program's sustainability was at risk. The necessity of addressing burnout among palliative care clinicians is well-established. (11, 16) Briefly, burnout is a syndrome resulting from chronic workplace stress.(17) It is characterized by feelings of energy depletion or exhaustion, mental distancing or negativity related to work, and reduced professional efficacy. The evolution and relative prevalence of each of these experiences vary. In the palliative care community, burnout is predominantly characterized by energy depletion and corresponding emotional exhaustion.(11) Individual factors associated with higher burnout include nonwhite race, female sex, and younger age. (18) (19) (20) Workplace factors associated with higher burnout exist at the systems-level (e.g., productivity-based performance evaluations) and at the job-level (e.g., lack of control over schedule). (11, (18) (19) (20) (21) Burnout is commonly accompanied by related experiences of moral distress and compassion fatigue. (18) Moral distress is the experience of psychological distress in response to a situation where a worker feels disempowered to do what they believe to be the morally appropriate action due to real or perceived job constraints. (22) Compassion fatigue is not, as the name would imply, an exhaustion of compassion towards others. Rather, it is a type of secondary traumatic stress defined by the emotional strain of working with those who are suffering from the consequences of traumatic events like serious illness. (23) Taken together, palliative care researchers are at high risk for burnout, moral distress, and compassion fatigue. Consider the experience of the young CRC who feels an obligation to complete certain tasks or has little control over their schedule. Consider the experience of the interventionist who feels a need to resist their psychology training in responding to a patient's distress, instead focusing on adhering to an intervention script. Consider the biostatistician who distances themself from the work because it was reminiscent of their own trauma. Consider the qualitative analyst who vicariously experiences and then carries the grief of bereaved parents. Consider the early career investigator who constantly struggles with their uncertain future. Consider the program leader who feels responsible for the whole team. Importantly, burnout, moral distress, and compassion fatigue are not necessarily persistent. While they certainly may be resolved with a job change or change in work-place responsibilities, they can also be addressed with targeted coping strategies.(24) We define resilience as "the process of harnessing the resources needed to sustain well-being in the face of stress or adversity." (25) (26) (27) This definition is grounded in resilience theory and decades of our and other teams' research. Indeed, during adversities as variable as illness, natural disaster, poverty, and war, people tend to draw from the same three buckets of resilience resources: (1) "Individual" resources (e.g., personal characteristics such as grit, hardiness, humor, optimism and skills such as stress-management, mindfulness, goal-setting, and self-compassion); (2) "Community" resources (e.g., social networks, support from peers, family, or faith-communities); and, (3) "Existential" resources (e.g., skills in re-appraisal and re-framing what matters, the search for meaning and purpose, the ability to reflect and learn lessons after adversity). (25) Which bucket of resilience resources most helps which person or group is highly variable. Hence, two key aspects of building resilience are identifying one's go-to buckets ("where do I already have resilience resources?", or more simply, "what do I do that helps me navigate tough times?"), and, diversifying one's resilience resource portfolio ("which of these buckets is relatively empty, and how can I fill it?") Asking these questions implies not only that the process of resilience must be deliberate, but also that resilience can be learned. (25) Finally, it is important to note that resilience, like burnout, is fluid. (25) The process evolves over time and may vary depending on the type of adversity. Resilience is not the opposite of burnout, rather, it may buffer the impact of burnout or it may be what we leverage to weather experiences like burnout. In our experience, the first phase of the process of resilience is recognizing the stressor and then normalizing and accepting our emotional response to it. We call this phase "getting through." This is a particularly important phase for navigating challenging feelings like moral distress and compassion fatigue. Experiencing them does not mean we are not resilient. It means we are currently, and perhaps with good reason, having a hard time. A key to successfully "getting through" is a culture of psychological safety. Leaders who demonstrate vulnerability, compassion, integrity, transparency, and commitment to their people can more successfully support team-members in this phase. We call the second phase of resilience the "harnessing resources" phase. This is when we contemplate how to move forward. Here, actions and thoughts must be deliberate and might include cultivating skills in stress-management, emotional awareness, mindfulness, self-compassion, goal-setting, and cognitive reframing. This phase takes work, time, and practice. To support their teams, leaders may need to prioritize these skills and create opportunities for team-members to develop them. (25) The third and final phase of resilience ("looking back and learning") comes when we are able to reflect on the impact of an experience on our identities, goals, and values. It is when we note the lessons we learned, the perspectives we gained, the things for which we are not grateful, and the ways in which we want to comport ourselves in the future. Here, leaders can facilitate this phase by providing opportunities for shared reflection and identity-building. (25) We target resilience in our palliative care research program because we believe it is a pathway to achieving palliative care's goals of alleviating suffering and improving quality of life. Once we recognized that our team was struggling, we also recognized that our team's resilience resource buckets demanded attention. Identify the "Why." Business and executive literature suggest that full and selfless focus on the best interests of individual colleagues and employees is the best way to inspire commitment and ensure success.(28) Helping individuals and teams identify their meaning, purpose, passion, and direction facilitates engagement and productivity. With this in mind, we gathered perspectives and conducted a series of workshops to identify individual and shared needs, goals, and values. As a group, we decided that the mission of our palliative care research program was "to develop evidence-based interventions to promote resilience, alleviate suffering, and improve quality of life among children with serious illness and their families." We broadly defined "interventions" to include formal protocoled packages like our resilience training program, as well as tools to support communication, decision-making, psychosocial and spiritual needs, and symptom-management among both patients and families and health-care personnel. We then explored how each member of the research program could align their own, personal mission with that of our shared work. Next, the full research team identified 6 team "core values" to serve as the foundation for our culture Identify the "What." After establishing our mission and values, we conducted an assessment of the team's resilience resources using the framework of our prior research. (26, 29) Notably, group or organizational resilience resources may be different from individual resources.(25) As a group, instead of asking "who helps me when times are tough?" we asked "how do we help each other?" We followed these questions with an exploration of what we "should" do to bolster each category of resources. Finally, we created a plan that integrated attention to each of these categories for both individual members of the research program, as well as for the whole group (Figure 2) . For example, we recognized that individual (personal) resources would strengthen with consistent focus on how to meet each person's career development goals. Developing individual and group skills in stress-management and self-care provided a buffer to the invariable stressors palliative care research teams experience. Group support for bereavement and difficult encounters bolstered the team's community (group) resilience resources, and attention to individual and group sense of purpose strengthened existential resources. Creating a norm where all group members felt empowered to speak during meetings facilitated a sense of community and recognition that our diversity of perspective and experience made us stronger. Identify the "How." Ultimately, we needed to determine how to creatively foster team resilience and fill our respective resilience resource buckets. Leveraging the multidisciplinary expertise of the team, we designed and implemented a curriculum called "Check, Act, Resilience, Engagement" (CARE, Figure 3 ). Briefly, CARE sought to address the needs we most often heard were unmet on the team: dealing with grief and loss, maintaining work-life balance, recognizing and navigating burnout, strategies for stress-management and self-care, skills in mindfulness and self-compassion, and integrating religion, spirituality, and the search for meaning and purpose into our daily work. Since then, it has expanded to include new challenges as they arise within the team and our broader community. In the past year for example, we held workshops focused on trauma stewardship, the experience of bias, racism, and sexual harassment, the stress and uncertainties brought on by COVID-19, and how to be anti-racist. CARE topics are addressed as brief workshops during research program meetings as often as once quarterly, and in more depth at twice-annual retreats. Team members share the responsibility of signing up for a topic they have either experienced, want to learn about, or both. They work independently or with internal or external mentors, based on their preference and style, to "present" the topic and provide a foundation for open discussion and shared resilience-building. Materials from each presentation are archived and available to the team. To date, the program has been feasible and highly valued. Since the implementation of our shared mission, core values, and procedures to build resilience in 2017, our team has had zero turnover due to burnout or distress. We have, however, experienced turnover for other reasons: two of our first CRCs left to attend graduate school with celebration from the rest of the team. Each person has continued to remotely join research program meetings for learning and professional development, citing the culture as critically helpful to their learning. Other staff have successfully shifted their roles to meet career development goals. Additional change has been in growth; several students who started as volunteers applied for entry-level CRC or interventionist jobs on the team, and we have tripled in size. Moreover, the program now supports several early palliative care researchers and clinicians across the country. All members routinely participate in research program and other meetings. Our leadership team has grown, too, and includes members representing the various professional roles of our team, including CRCs, interventionists, methodologists, and investigators. Where it may seem that the increased activities created to build our team's resilience would increase the leadership workload, our experience has been the opposite. Investing in team well-being paid off; turnover is lower, and engagement, productivity, and sense of commitment are higher. For example, as part of our 5-year anniversary, we asked all team members to answer the question: "In one word, what do you most appreciate about the Palliative Care and Resilience Research program?" Twenty-three members responded and provided answers like "community," "compassion," "courage," and "passion" (Figure 4) . In the first few years after we launched our palliative care research program, burnout, moral distress, compassion fatigue, and turnover were high. To address our sustainability and create a thriving team, we translated resilience theory to practice by identifying and championing shared mission and values, building group resilience resources, and targeting unmet needs. Since then, we have come together, grown, and flourished. We weathered the first phase of the resilience process ("getting through"). Now, we are in a constant iterative cycle between the second two phases ("harnessing resources" and "looking back"). We have not learned everything we need to know or how to solve every problem; we have an approach that enables us to continue to learn and reflect together. Our conclusion? Conducting palliative care research can be personally and professionally challenging. Targeting person and program resilience helps champion the fact that it is also highly rewarding and meaningful work. None of the authors has a financial or other conflict of interest to disclose. This project was not supported by a particular funding mechanism; however, the authors would like to thank the University Team core values were determined by team consensus and designed to meet both individual and collective missions. 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